metricas
Cirugía Española (English Edition) Surgery for rectal cancer beyond the mesorectum: Indications, preparation, limit...
Journal Information
Vol. 103. Issue 9.
(September 2025)
Cite
Cite
Share
Download PDF
More article options
Visits
1658
Vol. 103. Issue 9.
(September 2025)
Special article
Full text access

Surgery for rectal cancer beyond the mesorectum: Indications, preparation, limits, and results

Cirugia por cáncer de recto más allá del mesorrecto: Indicaciones, preparación límites y resultados
Visits
1658
Blas Flor-Lorente, Mario J. de Miguel-Valencia
Corresponding author
mj.demiguel.valencia@navarra.es

Corresponding author.
Reference Unit for Abdominopelvic Oncologic Surgery (UR-COAP), Coloproctology Unit, General and Digestive System Surgery Department, La Fe University and Polytechnic Hospital, Valencia, Spain
This item has received
Article information
Abstract
Full Text
Bibliography
Download PDF
Statistics
Figures (5)
fig0005
fig0010
fig0015
fig0020
fig0025
Tables (3)
Table 1. Indications and contraindications of pelvic exenteration.
Tables
Table 2. Pelvic exenteration classification.52
Tables
Table 3. Clinical results of pelvic exenteration.
Tables
Special issue
This article is part of special issue:
Rectal Cancer Treatment: The Future is already the Present

Edited by: Dr. Calos Cerdán
Cirugía General y Aparato Digestivo. Unidad de Cirugía Digestiva. Hospital Universitario de la Princesa. Madrid
Dr. Matteo Frasson
Cirugía general. Hospital Universitario y Politécnico La Fe. Valencia

Last update: January 2026

More info
Abstract

Pelvic exenteration (PE) is a potentially curative surgical option for patients with locally advanced rectal cancer (LARC) orlocallyrecurrent rectal cancer (LRRC) involvingmultivisceralstructures. Originally conceived as a palliative procedure, advancements in surgical techniques and multidisciplinary management have broadened its indications, enabling R0 resections in over 60% of cases. Appropriate patient selection, based on advanced imaging and comprehensive functional assessment, is essential to optimize oncologic outcomes. Currently, the surgical indication is primarily determined by the reasonable possibility of achieving an R0 resection with acceptable morbidity in a suitable candidate, which may translate into high survival rates. Surgical planning should follow a compartmental approach and require close collaboration among colorectal, urologic, gynecologic, vascular, orthopedic, plastic, and reconstructive surgeons. Urinary, gynecologic, vascular, osseous, and soft tissue reconstructions are tailored to the tumour’s extent and the patient's individual needs. In selected cases, PE may be performed with palliative intent. Intraoperative radiotherapy (IORT) and minimally invasive approaches have emerged as valuable adjuncts. Long-term oncologic and functional outcomes are closely linked to the achievement of negative margins. While postoperative morbidity remains significant, mortality rates have declined in high-volume centres. Postoperative quality of life has become a key outcome, with increasing emphasis on patient-reported outcome measures (PROMs) to guide clinical decision-making. PE continues to challenge traditional limits of resectability, offering renewed hope to carefully selected patients.

Keywords:
Pelvic exenteration
Locally-advanced rectal cancer
Recurrent rectal cancer
R0 resection
Resumen

La exenteración pélvica (EP) representa una opción terapéutica potencialmente curativa para pacientes con cáncer de recto localmente avanzado (LARC) o recurrencia local (LRRC) con afectación multivisceral. Inicialmente concebida como un procedimiento paliativo, los avances técnicos y el enfoque multidisciplinar han ampliado sus indicaciones, permitiendo resecciones R0 en más del 60% de los casos. La correcta selección de pacientes, basada en estudios de imagen avanzados y una valoración funcional integral, es esencial para maximizar los beneficios oncológicos. En la actualidad, el límite de la indicación quirúrgica se establece en la posibilidad razonable de lograr una resección oncológica completa (R0) con una morbilidad aceptable en el paciente adecuado, lo que puede traducirse en tasas elevadas de supervivencia. La cirugía debe abordarse de forma compartimental y con la colaboración de múltiples especialidades. La reconstrucción urinaria, ginecológica, vascular, ósea y de tejidos blandos se adapta a la extensión tumoural y las necesidades del paciente. En casos seleccionados, la EP puede utilizarse con intención paliativa. La radioterapia intraoperatoria (IORT) y la cirugía mínimamente invasiva han demostrado ser estrategias complementarias prometedoras. Los resultados oncológicos y funcionales dependen en gran medida de la obtención de márgenes negativos. Aunque la morbilidad puede ser elevada, las tasas de mortalidad han disminuido en centros especializados. La calidad de vida posoperatoria se ha convertido en un parámetro clave, destacando el papel de las medidas reportadas por los pacientes (PROMs) en la toma de decisiones. La EP continúa desafiando los límites tradicionales de la resecabilidad, ofreciendo esperanza a pacientes seleccionados.

Palabras clave:
Exenteración pélvica
Cáncer de recto localmente avanzado
Cáncer de recto recurrente
Resección R0
Full Text
Introduction

Pelvic exenteration (PE) is a radical surgical procedure consisting of the en bloc multivisceral resection of at least two contiguous pelvic organs, with the goal of obtaining oncologically negative margins in cases of locally advanced or recurrent pelvic neoplasia.1,2 This technique has transformed the approach to patients previously considered inoperable, offering a curative possibility in complex settings with extensive tumour invasion.3,4

Initially described in 1948 by Alexander Brunschwig for the palliative management of recurrent cervical carcinoma, PE has evolved from a palliative approach to a viable curative option, particularly in the context of locally advanced primary rectal cancer (LARC) or locally recurrent primary rectal cancer (LRRC).1,5 Although high mortality rates and poor survival outcomes initially limited its adoption, advances in anaesthesia, transfusion, radiology, and surgical techniques have significantly improved the safety and efficacy of PE.3,5

Achieving malignancy-free surgical margins (R0) is considered the most determining factor in predicting both long-term survival and postoperative quality of life.3,6–9 Currently, both LARC and LRRC achieve R0 resection rates greater than 60%.10–13

Surgical planning by multidisciplinary committees, based on tumour topography and the prediction of invaded structures, optimises surgical outcomes.14,15 For tumour staging, the most commonly used techniques are magnetic resonance imaging (MRI), computed tomography (CT), and positron emission tomography (PET/CT), occasionally supported by 3D reconstructions.15

Given the radical nature of the procedure, there is a general consensus that PE should be reserved for cases of resectable disease with curative intent.7

Athough PE is mostly performed by laparotomy, laparoscopic and robotic approaches are becoming increasingly common.16 Perioperative management of PE requires a specialised and multidisciplinary approach, which has driven centralisation in high-volume units, favouring the standardisation of procedures and improving both oncological outcomes and morbidity, and thereby expanding the limits of resectability.2,7,8,17–19

In addition to surgical advances, the role of total neoadjuvant therapy (TNT) is being investigated, which enables improved adherence, early treatment of micrometastases, and disease downstaging, with higher rates of pathological complete response.20–23

With the safety and oncological outcomes of PE now established, the current focus is on quality of life, promoting better patient selection and more accurate preoperative counseling. PROMs (Patient Reported Outcomes Measures) have gained relevance as a key tool to assess the true impact of surgery from the patient's perspective, reinforcing the need for a comprehensive approach to cancer.24,25

Indications, contraindications, and evolving surgical limits

LARC and LRRC, which affect pelvic organs or adjacent bony or neurovascular structures, are the most common indications for PE.3,26

PE is more common in recurrent disease, due to the earlier diagnosis of the primary cancer.27 A multidisciplinary approach, multivisceral resection, and resection of important neurovascular and bone structures, along with reconstructive and rehabilitative techniques, have allowed for larger resections, reducing the impact on patient function and quality of life,26,28,29 and also improving long-term survival.26,28 Currently, the limit of surgical indication can be considered the reasonable possibility of achieving complete oncological resection (R0) with acceptable morbidity in the appropriate patient, achieving high survival rates,1,3,7,30,31 (Table 1).

Table 1.

Indications and contraindications of pelvic exenteration.

Indications 
Possibility of achieving R0 with acceptable morbidity:Locally advanced rectal cancer (LARC) or recurrent rectal cancer (LRRC) unresectable with standard TMEOther advanced pelvic tumoursPalliative PE (PPE)a for relief of intractable symptoms: pain, bleeding, sepsis, obstruction, or fistulas 
Relative contraindicationsb 
Resectable metastasesSacral S1 infiltrationExternal iliac vessel infiltrationGreater sciatic notch extension 
Absolute contraindications 
Bilateral sciatic nerve involvementCircular pelvic bone involvementUnresectable disseminated metastatic diseasePoor performance status or severe comorbidities (ASA > 3) 
a

There is currently no evidence of improved quality of life or long-term benefits of EPP; it is associated with significant morbidity and mortality.

b

Contraindications based on anatomical boundaries and technical limitations have lost relevance.4

Additionally, in selected cases, PE may be considered palliative care (PPE) with the intention of relieving debilitating symptoms, especially in patients with limited options after prior radiation therapy.3

PE is limited to patients with good general health,3,35 excluding those with poor functional status, defined as a score greater than 3 on the American Society of Anaesthesiologists (ASA) score.26

The role of PE in patients with metastatic disease is uncertain. The presence of distant metastases unsuitable for curative resection contraindicates PE, but if they are resectable, they can be considered a relative contraindication, and simultaneous liver resection is feasible. The decision should be individualisd, especially given the prolonged recovery time that may limit the administration of adjuvant chemotherapy.7,26,36–38

Historically, pelvic wall involvement was considered an absolute contraindication, particularly in patients with unilateral hydronephrosis and sciatic pain. However, technical advances and high-volume units have made it increasingly possible to perform extra-anatomical R0 resections, even in complex cases involving bone or vascular resections.7,26

Infiltration of the external iliac vessels, sacral infiltration above S2, and extension through the greater sciatic notch may be contraindications, although these are increasingly relative, as surgical complexity and the risk of poor outcomes increase.7,30,34,36

Absolute contraindications include bilateral sciatic nerve involvement or circumferential bone involvement, which are associated with adverse outcomes and technical limitations in achieving an R0 resection.34

Although the indications for this procedure have expanded significantly, careful patient selection remains essential to optimise outcomes.

Diagnosis and preoperative evaluation for pelvic exenteration in rectal cancer

A thorough multidisciplinary preoperative evaluation, including a concise perineal physical examination, including vaginal examination, colonoscopy, pelvic MRI, and even cystoscopy, is essential to confirm the diagnosis, assess for pelvic visceral involvement, and consider the possibility of achieving an R0 resection.39 Histological confirmation of malignancy is imperative for patients considered for PE for cancer.

In addition, the presence of metastatic disease should be assessed, and the patient's fitness to endure such a radical surgical procedure should be evaluated.39

MRI, CT, and PET/CT are essential for preoperative planning, assessing cancer spread and enabling accurate surgical mapping. These tests should be performed as close to the time of surgery as possible.9 High-resolution MRI is the test of choice for defining local spread to adjacent pelvic structures,7,15 since sensitivity and specificity are both very high.40 It also enables three-dimensional multiplanar volumetric reconstructions that aid in the assessment of tumour boundaries.18 CT of the chest, abdomen, and pelvis is the first-line modality for the detection of potential metastatic lesions. PET/CT complements this assessment by providing information on metabolic activity and tumour spread in the pelvis, which can modify therapeutic decisions in up to 40% of cases.15,41,42 In addition, CT arteriography and venography are useful for planning pelvic resections.15 Radiological reports should be standardised, based on recent clinical guidelines.43,44

Currently, mathematical methods are being applied to MRI that make it possible to generate three-dimensional images of the pelvis, which define the optimal surgical plane for achieving R0 resections45 (Fig. 1). Furthermore, advances in artificial intelligence, three-dimensional bioprinting, radiomics, and radiogenomics promise to expand the limits of resections and improve diagnostic accuracy in oncologic surgery.11,46

Fig. 1.

Magnetic resonance images (coronal and sagittal sections) showing a tumour corresponding to a second pelvic recurrence of a rectal neoplasm with involvement of neighboring pelvic structures, including the vaginal vault, bladder, bowel loops, and left levator ani muscle. Below, a three-dimensional anatomical reconstruction (Cella Medical Solutions® proprietary software) allows precise spatial visualisation of tumour extension and its relationship to organs and vascular structures, facilitating surgical planning in complex cases of pelvic exenteration.

Preoperative medical optimisation with a multidisciplinary approach that includes nutrition, ostomy therapy, physical therapy, thromboembolic prophylaxis, and planned anesthetic techniques is essential for managing surgical stress.47–49 Psychosocial assessment helps determine the patient's ability to tolerate the after-effects of the procedure and prolonged recovery.39 Patient involvement in decision-making and prehabilitation improves outcomes.50

The implementation of ERAS (Enhanced Recovery After Surgery)-based protocols is feasible in PE and can optimise postoperative recovery, with adherence rates exceeding 70%.51

Surgical technique

PE is the en bloc resection of at least two contiguous pelvic organs to achieve negative margins in advanced neoplasia.52 Standardising PE techniques is challenging due to variability in tumour extensión. However, the systematic division of the pelvis into five anatomical compartments (central, anterior, posterior, and two lateral) facilitates a more organised and precise surgical approach.[18] Resection should include the entire compartment when an organ is involved to minimise positive margins (Table 2) (Fig. 2).7 Tumour recurrence adds technical complexity, frequently compromising deep muscular, osseous, and neurovascular structures.18

Table 2.

Pelvic exenteration classification.52

Type of Exenteration  Description 
Total (EPT)  Resection of all pelvic organs 
Anterior  Resection of the bladder and gynecological organs in women, preserving the rectum 
Posterior  Resection of the rectum and gynecological organs in women, preserving the bladder 
Supraelevator  Resection of the levator ani muscles and the anorectal stump 
Infraelevator  Resection of the levator ani muscles and the anorectal stump 
Comppsite  Includes resection of additional structures: blood vessels, lymph nodes, muscles, or bones 
Fig. 2.

Images A and B: Sagittal and coronal sections of a pelvic MRI of a patient, illustrating the different types of pelvic exenteration according to the structures included in the resection. Image C: Coronal section of a male patient.

The orange perimeter delineates an anterior exenteration, which includes the bladder and, in women, the internal genital organs. The blue perimeter corresponds to a posterior exenteration, which affects the rectum (and also the genital organs in women). The red perimeter represents a total pelvic exenteration, which includes resection of the bladder, rectum, and genital organs. The yellow lines indicate additional structures that may be included in a compound exenteration, such as the levator muscles or bony structures. Finally, the green line indicates the plane of the levator muscles, serving as a reference for classifying the exenteration as supralevator or infralevator, depending on whether these muscles are spared.

Exteriorisation of a colostomy is standard practice, although intestinal continuity can be restored through a coloanal anastomosis and temporary diverting ileostomy if adequate margins are present.39

The success of the technique lies in the coordinated participation of various specialists to comprehensively address the challenges of PE. In addition to the colorectal surgeon, the team should include urologists, spinal trauma specialists, gynecologists, radiation oncologists, vascular surgeons, and reconstructive surgeons, both plastic and abdominal wall.

Anterior compartment

Bladder involvement in PE may require partial cystectomy (PC) or radical cystectomy (RC). PC achieves good oncological results in patients with LARC and should be considered if technically feasible. In LRRC, en bloc RC improves oncological control and preserves quality of life. Reinterventions are more common in PC, although wound-related complications are lower.53

In women, involvement of the posterior vaginal wall is common, necessitating partial vaginectomy and, in some cases, hysterectomy. In men, when the tumour penetrates Denonvilliers' fascia, it can invade the prostate, seminal vesicles, and membranous urethra, generally requiring prostatectomy and/or en bloc cystectomy.18 However, in selected cases, bladder preservation is possible, avoiding complications associated with reconstruction.54 Tumours infiltrating the pubic bone and membranous urethra, previously considered inoperable, can now be treated with curative intent.3,27 A transperineal approach has been developed for urethral resection, with or without en bloc resection of the pubic bone, which allows for a wider anterior margin compared to the traditional abdominal approach, reducing the risk of positive margins.18,30,55,56 Both radical resection of the pubic bone and urinary reconstructions pose a significant risk of morbidity.30

Posterior compartment

Involvement of the posterior pelvic compartment includes, in addition to the rectum, the presacral space, and the sacrococcyx.

Sacral involvement above S2-S3 limited the indication for PE due to its technical complexity, morbidity, and functional sequelae from nerve root sacrifice.57 However, technical modifications have reduced morbidity58,59 and allowed for "higher and wider" resections, even down to the S1 roots, with results comparable to low sacrectomy.60,61

Sacral bone preservation can be achieved by accessing the presacral plane through the presacral fascia, above the level of the tumour, using a high subcortical sacrectomy,18,62 although segmental sacrectomy techniques have also been described.59 However, an en bloc sacrectomy may be essential in situations of perforation, sepsis in the posterior compartment, or tumour invasion of the bone or its fascia.18,30 In cases of recurrence after total mesorectal excision (TME) surgery, there is usually no defined anatomical plane between the tumour and the sacrum, which implies the need for sacrectomy in most patients.18

Sacrectomies are classified as low (S3 and below) and high (S2 and above). While low sacrectomies can be approached by abdominolithotomy or in the prone position, high sacrectomies frequently require the prone position to optimise visualisation and access to the pelvic wall, thus facilitating control of the iliac vasculature and a lateral dissection of the lumbosacral trunk and sacral roots.18,58,61,63

Some studies indicate that the level of sacrectomy does not impact either the length of hospitalisation or the rate of involved margins.64,65 However, a systematic review indicates that higher resections carry a higher risk of major complications.66

Lateral compartments

Resection of the lateral compartment of the pelvis is complex due to the proximity of key neurovascular structures, such as the lumbosacral trunk, sciatic nerve, and iliac vessels. Historically, tumours in this area have had low R0 resection rates and poorer survival, but this approach is now safe in specialised centres.28,29,67 Lateral dissection may be necessary to perform en bloc resections,30,68 in cases of suspicious lymphadenopathy, for bilateral vascular control prior to sacrectomy, or when tumour extension involves structures such as the sacral roots, piriformis and obturator internus muscles, and the sciatic nerve.18 Pelvic sidewall fibrosis, which develops after chemoradiotherapy, can hamper vessel-sparing lymphadenectomy and increases the risk of bleeding which is why en bloc excision is considered a safer option.28 In advanced tumours involving the pelvic sidewalls, ligation and resection of the internal iliac vessels is frequently performed and is usually well tolerated without reconstruction, as it is often accompanied by a central exenteration in which dependent organs are removed.63,68 Bilateral ligation has been described as a safe and effective technique to prevent and help control bleeding in pelvic surgeries.69 However, when resection of the common or external iliac artery or vein is necessary, reconstruction is essential to preserve limb perfusion,18,68 although major complication rates can reach up to 70%.68 Laterally extended endopelvic resection (LEER) is a surgical technique that facilitates R0 resections and more effective locoregional tumour control, especially in cases where the tumour is fixed to the pelvic wall. This technique involves multicompartmental resection of various pelvic parietal structures, such as paravisceral fat and pelvic floor muscles. It also allows for the removal of the overlying parietal endopelvic fascia, which acts as a barrier to tumour progression.70 However, LEER is not indicated for tumours infiltrating above the level of the obturator nerve or in the sciatic foramen. The technique is frequently combined with therapeutic periaortic and pelvic lymphadenectomy for more complete regional tumour control.70

Despite reservations about extended lateral compartment excision, especially en bloc resection of the femoral or sciatic nerves due to its morbidity and functional impact, oncological outcomes are promising. A radical approach improves R0 rates and survival. In some cases, resection of the sciatic spine optimises exposure and access to the sciatic nerve.18

The diagnosis and management of lateral pelvic lymph nodes (LLNs) is crucial, as their involvement increases the risk of local recurrence. Currently, nodes in the internal iliac and obturator regions are considered regional and should be included in the dissection, while nodes in the external and common iliac regions are classified as metastatic. Despite the differences between Western and Eastern approaches, there is consensus that the combination of neoadjuvant chemoradiotherapy (nCRT) and selective LLN dissection (LLND) reduces the risk of local recurrence and improves long-term outcomes. A surgical approach based on fascial planes rather than blood vessels is preferred, which better protects pelvic autonomic nerves and reduces the risk of postoperative male urinary and reproductive dysfunction.71–73 Transanal-assisted LLND has been reported to offer advantages over the traditional transabdominal approach.74

With the advent of TNT, response rates have improved, raising questions about the management of LLNs and the need for their selective dissection. Although LPLND reduces local recurrence, it has not been shown to improve overall or disease-free survival, requiring individualised patient selection.71–73

Intraoperative radiotherapy (IORT)

Neoadjuvant chemoradiotherapy is key in primary and recurrent rectal cancers without prior radiotherapy, reducing tumour stage and local recurrence.75 Re-irradiation, although controversial due to its cumulative toxicity, improves survival with emerging techniques that optimise tumour dose without affecting healthy tissue. Its application requires precise field delimitation, adequate fractionation, and adjustment according to the interval between treatments.75,76

IORT, in its different modalities, allows for the administration of high doses (10–20 Gy) to the tumour bed after resection, minimising exposure to healthy tissue, unlike external beam radiation therapy (EBRT) (45–50 Gy). Furthermore, it has been shown to achieve excellent local control, improving disease-free survival and overall survival, without a significant increase in serious complications.77–80 IORT is especially useful in the context of pelvic exenteration (PE), although its routine use is not recommended, reserving it for areas with a high risk of local recurrence, especially in R1 resections or with compromised margins, either preoperatively or intraoperatively.63,77,79–83 Its application is more appropriate in patients who can assume a higher risk of complications in exchange for reducing recurrence.80 Its usefulness in macroscopic residual disease (R2) is limited.77 (Fig. 3).

Fig. 3.

Intraoperative radiotherapy (IORT) in patients undergoing pelvic exenteration. There are three types of IORT: intraoperative electron beam radiotherapy (IOERT) like imaging, high-dose-rate intraoperative brachytherapy (HDR-IORT), and low-kilovoltage IORT. IOERT has faster treatment times, simpler preparation, and greater tissue penetration. HDR-IORT, with more flexible applicators that better adapt to the pelvis, delivers more concentrated doses, but the treatment time is longer. Kilovoltage IORT has less penetration, requires less shielding, but its applicator is fixed and the treatment time is slower.80

(A) Case 1: IORT administration via laparotomy.

(B and C) Case 2: patient in the prone position, with IORT directed toward the lateral wall of the pelvis.

The role of minimally invasive surgery (MIS)

MIS, both laparoscopic and robotic84,85 has significantly advanced in pelvic procedures, showing similar mortality results compared to open approaches via laparotomy,86,87 which remains the most common approach. With increasing experience in MIS PE, a reduction in morbidity is expected.88 Studies consider it a safe and viable option in patients with favorable anatomy and tumours, offering lower blood loss and shorter hospital stays, albeit with longer surgical times.87,88

Genitourological reconstruction

There is no ideal urinary reconstruction, so it must be tailored to each patient. Urinary reconstruction options include proximal transection and reimplantation of the ureters, with or without a Boari flap, or ureterovesical reconstruction with an interposed ileal loop after partial cystectomy if the residual bladder volume is adequate to preserve bladder function. or a urinary diversion via an ileal (Bricker) conduit or colonic conduit in the case of radical cystectomy.18,30,89 More recent alternatives include the continent urostomy, which uses the transverse colon and ileum,39 and the increasing use of wet double-barrel colostomies in patients with short ureters or anatomical difficulties.90 Wet double-barrel colostomy simplifies management by unifying the diversions into a single stoma, reduces the risk of complications by avoiding intestinal anastomosis, separates faecal and urinary flows (compared to traditional wet colostomy), and promotes a faster recovery,91,92 As a last resort or temporary solution, cutaneous ureterostomy or nephrostomy may be used, although they carry considerable long-term morbidity due to the need for percutaneous drainage and frequent catheter changes.18 The use of intraoperative ureteral catheters facilitates their identification and protection.18 (Fig. 4).

Fig. 4.

Urinary reconstructions. Image A: construction of an inverted wet colostomy. Image B: reconstruction using ileal loop interposition (bilateral ureter-ileum-bladder anastomosis).

Various techniques exist for the reconstruction of vaginal defects, ranging from the use of skin grafts or isolated segments of bowel to rectus abdominis myofascial flaps, deep inferior epigastric artery perforator (DIEP) flaps, bilateral flat gracilis flaps, or specialised gluteus maximus flaps.39,93

Bone Reconstruction/Stabilisation

The functional benefits of bone reconstruction must be weighed against the risks of prolonged operative time, wound or prosthesis/allograft infections, and nonunion or bony nonunion. Prior radiation therapy limits prosthesis integration, so adequate soft tissue coverage is essential for any type of prosthesis. Biological reconstruction is preferable to prosthetic reconstruction in patients with high functional demands, as well as in those who cannot undergo frequent radiological and/or clinical follow-up.18 Although several fixation methods exist, there is no evidence to suggest the superiority of one over another.94

Vascular reconstruction

Vascular reconstruction is complex due to the presence of irradiated and contaminated tissue, which increases the risk of infection in synthetic grafts. The optimal method for vascular reconstruction has not yet been established. Autologous grafts, such as the great saphenous vein, are widely used due to their lower risk of thrombosis and infection, although they have limitations such as availability and differences in lumen size.68 For this reason, the use of vascular prostheses is also widespread. An alternative, although expensive, is the bovine biological graft. 81

To avoid ischaemia or compartment syndrome in the extremities, arterial reconstruction should be performed immediately.95 Recently, innovative approaches have been described that promote preventive grafting (crossed femoral-femoral95,96 or axilofemoral97 weeks before PE, reducing the risk of septic graft complications, total surgical time, and ischemia in the lower limbs.

Soft tissue reconstruction

Closure options include primary repair (with or without the use of an omental pedicle), the use of biological or synthetic mesh to reconstruct the pelvic floor, autologous myocutaneous flaps, or the use of breast prostheses.81 However, evidence on the optimal technique remains limited.48

Reconstructive techniques vary depending on the affected region: for abdominal defects, rectus abdominis (VRAM)/ORAM flaps are used; for the gluteus, VY flaps or gluteal artery perforator flaps; for the thigh, anterolateral flaps with or without the vastus lateralis or bilateral gracilis; and for the gluteal/perineal fold, pudendal artery or perineal rotation flaps.l98 The VRAM/ORAM flap is one of the most common options due to its ease of harvest and robustness.48,81

Biological mesh, usually anchored at the level of the pubic symphysis and the sacral promontory, is a quick and safe option that prevents the small intestine from protruding into the pelvis and reduces the rate of hernias in the short term.99,100 (Fig. 5)

Fig. 5.

Perineal reconstructive techniques after pelvic exenteration. In both cases, Permacol® biological mesh is used, secured with interrupted, non-absorbable monofilament sutures in a crown-shaped pattern. Skin and subcutaneous tissue closure is performed by the Plastic Surgery team using a V-Y advancement flap (case A) and a double V-Y flap (case B).

An emerging technique is the use of 3D-printed, custom prostheses specifically tailored to each patient's defects.101

Palliative Pelvic Exenteration (PPE)

PPE may be considered, exceptionally, without curative intent in patients with severe and intractable local symptoms—such as refractory pain, persistent bleeding, fistulisation into neighboring organs or the abdominal wall, and intestinal obstruction—when all conservative therapeutic alternatives have failed 32,102

In these selected cases, the patients should have a reasonable life expectancy and good functional status, who fully understand and accept the magnitude of the surgery and its sequelae, despite the lack of direct oncological benefit.

Although it can offer symptomatic relief in extreme scenarios, PPE remains a controversial procedure due to its high morbidity, its limited impact on survival, and the possible lack of recovery in quality of life, which tends to progressively deteriorate until death.32,33,39,81 Further studies are needed to more precisely define its indication and potential benefits.32

Results

The aetiological diversity, the multiple surgical technical options—including different types of pelvic exenteration (total, anterior, or posterior)—and the lack of standardisation in outcome measurement make comparative studies and meta-analyses difficult, resulting in highly variable figures in the literature.103 This technical variability significantly influences morbidity and survival, and interpreting results without considering these differences can be misleading. Coordinated international collaboration is needed to define key outcome sets, surgical classification criteria, and benchmarks that allow for more rigorous comparisons.103

Pelvic exenteration (PE) has a high overall morbidity, with rates ranging from 18% to 87%.7,10,31,104–106 These are particularly high in patients with local recurrence (LRRC: 82%) versus primary disease (LARC: 47%).104,105 The most common complications include infections, urinary or intestinal leaks, sepsis, and flap-related complications, with major complication rates ranging from 16.4% to 34.4%.107,112 Empty pelvis syndrome (EPS), responsible for up to 40% of postoperative complications, is associated with large resections and prior radiation therapy.48,99,109,115 The R0 resection rate varies widely by setting: up to 80% in LARC and 60% in LRRC.10–13,117,118

Despite its complexity, in-hospital mortality is low in specialised centres (1–5%),3,9,12,121 and 5-year survival rates reach up to 67% in some studies.9,106,122 Tumour recurrence, however, can affect up to 68% of patients, and may be local, distant, or combined.10 Quality of life after PE usually recovers progressively, especially in patients with R0 resection, and acceptable functional adaptation has been described in most cases,49,106,125,126 with variable impact on continence, urinary and sexual function, pain, and return to work.81

Table 3 presents a detailed summary of the results obtained after pelvic exenteration, along with key considerations that should be taken into account in the interpretation of these data.

Table 3.

Clinical results of pelvic exenteration.

Category  Results and clinical commentas 
Morbidity  Total: 18–87%7,10,31,104–106LARC: 47%, LRRC: 82%104,105Immediate postoperative: 40%9,107Risk factors: previous chemoradiotherapy, pelvic dead space, low tissue vascularisation, bacterial contamination92,108 
Hospìtal stay  Median: 9−29 days106 
Reinterventions  Long-term up to 17%106,109 
Common complications  Variable figures 3,92,106,110,111: sepsis, perineal wound infection, urinary complications (leaks, UTIs), gastrointestinal complications (anastomotic leaks), flap complications 
Major complications (Clavien-Dindo III-IV)  34.4% (n = 195)112; 16.4% (n = 604)107Intra-abdominal collections: up to 43.7%Woundinfection: 14%Sepsis: 3.7%–8.2%Iintestinal leak: 2.6–7.4%Urinary leak: 4.6%Postoperative bleeding: 4.4%–5.6%. 
Pain  High prevalence113,114It is not usually measured or managed adequately42Better control of R0 margins vs. R1/R2 margins or after bone resection114 
Empty Pelvis Syndrome (EPS)  Up to 40% of postoperativecomplications48,115Causes: residual void after multivisceral resection, intestinal displacement into the pelvis, pelvic floor dysfunction, impaired healing due to chronic ischaemia99,109Aggravating factors: prior radiation, devascularisation of skin flaps, large tissue defects, bone exposure (high sacrectomy, pubic resection)19,30,99,108EPS-associated complications: pelvic collections, prolonged ileus, mechanical bowel obstruction, perineal dehiscence, perineal sinuses, enteroperineal fistulas99,115,116Prevention: reconstructive techniques, although they are also associated with morbidity48,98,99,109In cases of symptomatic obstruction or fistulisation, it is preferable to isolate the fistula or perform bypass surgery, avoiding more invasive resections109 
R0 resection rate  LARC: up to 80%; LRRC: up to 60%10–13,117,118Recent systematic revision106: 23.2%–98.4% (LARC), 14.9%–77.8% (LRRC)Urological: 84.6% (primary), 73.6% (recurrences)10Gynecological: 87% (endometrium), 76% (vagina), 73% (primary cervix), 79% (recurrent cervix), 64% (primary ovary), 52% (recurrent ovary)10 
Tumour recurrence  Global: 3.2%–68%. Local: 4.3%–68%. Distant: 11%–46%. Combined: 3.2–61%10Re-exenteration can be considered a curative option30,118–120 
Mortality  Inpatient: 3.11%121At 30 days: 0–9.1%106,121Specialised centres: 1%–5%3,9,12 
Survival  Variable figuresNo differentiation between open surgery and MIS 87Survival: 1 year: >80%; 3 years: 20%–75%; 5 years: 8%–67%9,106,122Disease-free survival: 5 years: 13%–89%; 10 years: 17.4%–50%9,106,122Critical factors: R0 resection, bone resection if necessary, specialised centres10,122,123; radiotherapy improves R0 rates but not survival105 
Quality of life (QoL)  Acceptable, with gradual recovery after the immediate postoperative period49,106,125R0 offers better long-term outcomes; most patients manage to adapt and maintain a stable functional status126Physical, functional, emotional, and social dimensions: urinary and sexual function, continence, pelvic pain, musculoskeletal function, and employability81 

In recent years, the approach to PE has transcended morbidity and survival, incorporating quality of life and PROMS as key parameters for individualising treatment according to patient needs. These are standardised instruments that allow direct collection, through questionnaires, of patient perceptions of their physical, emotional, functional, and social health after surgery. In the case of PE, several studies have shown a significant impact on aspects such as urinary and sexual function, continence, pelvic pain, mobility, and return to work, especially in the first postoperative months. The outcome of these indicators may improve over time, depending on rehabilitation support and individual adaptation.23,24,109,124

Although annual volume is not the only indicator of quality, centres with more than 20 pelvic exenterations per year—considered high-volume—have shown better outcomes, supporting centralisation in specialised units and strengthening referral pathways to tertiary centres with established multidisciplinary teams.17

Conclusions

Pelvic exenteration (PE) has become established as a curative therapeutic option for advanced or recurrent pelvic cancers, with R0 margins being the primary objective for improving survival. Advances in imaging, surgical techniques, and multidisciplinary management in specialised high-volume units have expanded the indications, improving oncological and functional outcomes with reduced morbidity. Furthermore, the integration of tools such as PROMS has reinforced the need for a comprehensive approach that considers not only tumour control but also patient quality of life.

References
[1]
B. Lampe, V. Luengas-Würzinger, J. Weitz, et al.
Opportunities and limitations of pelvic exenteration surgery.
Cancers (Basel)., 13 (2021),
[2]
R.L. Venchiarutti, M.J. Solomon, C.E. Koh, J.M. Young, D. Steffens.
Pushing the boundaries of pelvic exenteration by maintaining survival at the cost of morbidity.
Br J Surg., 106 (2019), pp. 1393-1403
[3]
K.G.M. Brown, M.J. Solomon, C.E. Koh.
Pelvic exenteration surgery: the evolution of radical surgery techniques for advanced and recurrent pelvic malignancy.
Dis Colon Rectum, 60 (2017), pp. 745-754
[4]
M.J. Solomon, K.G.M. Brown.
Extended radical resection: the standard of care for patients with advanced pelvic malignancy.
Ann Surg Oncol, 27 (2020), pp. 323-324
[5]
A. Brunschwig.
Complete excision of pelvic viscera for advanced carcinoma; a one-stage abdominoperineal operation with end colostomy and bilateral ureteral implantation into the colon above the colostomy.
[6]
S.U. Saqib, M.Z. Raza, J. Twigg, O. Altan, A.A. Bajwa.
Feasibility of robotic platform to perform R0 resection for locally advanced multi-visceral pelvic malignancy: an institutional experience on outcomes of robotic pelvic exenteration.
Langenbecks Arch Surg., 409 (2023), pp. 9
[7]
C.E. Koh, M.J. Solomon, K.G. Brown, et al.
The evolution of pelvic exenteration practice at a single centre: lessons learned from over 500 cases.
Dis Colon Rectum., 60 (2017), pp. 627-635
[8]
D. Steffens, M.J. Solomon, J.M. Young, et al.
Cohort study of long-term survival and quality of life following pelvic exenteration.
BJS Open, 2 (2018), pp. 328-335
[9]
PelvEx Collaborative.
Surgical and survival outcomes following pelvic exenteration for locally advanced primary rectal cancer: results from an international collaboration.
Ann Surg, 269 (2019), pp. 315-321
[10]
PelvExCollaborative.
Pelvic exenteration for advanced nonrectal pelvic malignancy.
Ann Surg., 270 (2019), pp. 899-905
[11]
PelvEx Collaborative.
Contemporary management of locally advanced and recurrent rectal cancer: views from the PelvEx Collaborative.
[12]
E. Platt, G. Dovell, S. Smolarek.
Systematic review of outcomes following pelvic exenteration for the treatment of primary and recurrent locally advanced rectal cancer.
Tech Coloproctol, 22 (2018), pp. 835-845
[13]
L.C. de Nes, J.A. van der Heijden, M.G. Verstegen, et al.
Predictors of undergoing multivisceral resection, margin status and survival in Dutch patients with locally advanced colorectal cancer.
Eur J Surg Oncol, 48 (2022), pp. 1144-1152
[14]
Z. Rokan, C. Simillis, C. Kontovounisios, B.J. Moran, P. Tekkis, G. Brown.
Systematic review of classification systems for locally recurrent rectal cancer.
BJS Open, 5 (2021),
[15]
P.I. Causa Andrieu, S. Woo, E. Rios-Doria, Y. Sonoda, S. Ghafoor.
The role of imaging in pelvic exenteration for gynecological cancers.
Br J Radiol, 94 (2021),
[16]
S. Cianci, M. Arcieri, G. Vizzielli, et al.
Robotic pelvic exenteration for gynecologic malignancies, anatomic landmarks, and surgical steps: a systematic review.
Front Surg., 8 (2021),
[17]
PelvEx Collaborative.
Changing outcomes following pelvic exenteration for locally advanced and recurrent rectal cancer.
BJS Open, 3 (2019), pp. 516-520
[18]
PelvEx Collaborative.
Minimum standards of pelvic exenterative practice: PelvEx Collaborative guideline.
Br J Surg., 109 (2022), pp. 1251-1263
[19]
A.S. Jacombs, P. Rome, J.D. Harrison, M.J. Solomon.
Assessment of the selection process for myocutaneous flap repair and sur gical complications in pelvic exenteration surgery.
Br J Surg., 100 (2013), pp. 561-567
[20]
R.R. Bahadoer, E.A. Dijkstra, B. van Etten, RAPIDO collaborative investigators, et al.
Short-course radiotherapy followed by chemotherapy before total mesorectal excision (TME) versus preoperative chemoradiotherapy, TME, and optional adjuvant chemotherapy in locally advanced rectal cancer (RAPIDO): a randomised, open-label, phase 3 trial.
Lancet Oncol, 22 (2021), pp. 29-42
[21]
P. Goffredo, A. Khan, S.L. Mott, et al.
Total neoadjuvant therapy versus standard neoadjuvant chemoradiation in patients with locally advanced rectal cancer: a comparison of short- and long-term oncologic outcomes.
Ann Surg., 276 (2022), pp. e819-e824
[22]
G. Turri, G. Ostuzzi, G. Vita, et al.
Treatment of locally advanced rectal cancer in the era of total neoadjuvant therapy: a systematic review and network meta-analysis.
[23]
A. Cercek, C.S. Roxburgh, P. Strombom, et al.
Adoption of total neoadjuvant therapy for locally advanced rectal cancer.
JAMA Oncol., 4 (2018),
[24]
K.G.M. Brown, M.J. Solomon.
Understanding quality of life after pelvic exenteration for patients with rectal cancer.
Ann Surg Oncol, 31 (2024), pp. 7668-7670
[25]
K. Meadows.
Patient-reported outcome measures—A call for more narrative evidence.
J. Patient Exp, (2021),
[26]
C.S. van Kessel, M.J. Solomon.
Understanding the philosophy, anatomy, and surgery of the extra-TME plane of locally advanced and locally recurrent rectal cancer; single institution experience with international benchmarking.
Cancers (Basel)., 14 (2022),
[27]
P.S. Waters, O. Peacock, S.K. Warrier, et al.
Evolution of pelvic exenteration surgery- resectional trends and survival outcomes over three decades.
Eur J Surg Oncol., 45 (2019), pp. 2325-2333
[28]
M.J. Solomon, K.G.M. Brown, C.E. Koh, P.J.M. Lee, K.K.S. Austin, L. Masya.
Lateral pelvic compartment excision during pelvic exenteration.
Br J Surg, 102 (2015), pp. 1710-1717
[29]
M. Kazi, V. Sukumar, A. Desouza, A. Saklani.
State-of-the-art surgery for recurrent and locally advanced rectal cancers.
Langenbeck’s Arch. Surg., 406 (2021), pp. 1763-1774
[30]
Y.C. Lau, K.G.M. Brown, P. Lee.
Pelvic exenteration for locally advanced and recurrent rectal cancer-how much more?.
J Gastrointest Oncol, 10 (2019), pp. 1207-1214
[31]
J.M. Young, T. Badgery-Parker, L.M. Masya, et al.
Quality of life and other patient-reported outcomes following exenteration for pelvic malignancy.
Br J Surg, 101 (2014), pp. 277-287
[32]
PelvEx Collaborative.
Palliative pelvic exenteration: a systematic review of patient-centreed outcomes.
Eur J Surg Oncol., 45 (2019), pp. 1787-1795
[33]
A.J. Quyn, M.J. Solomon, P.M. Lee, T. Badgery-Parker, L.M. Masya, J.M. Young.
Palliative pelvic exenteration: clinical outcomes and quality of life.
Dis Colon Rectum., 59 (2016), pp. 1005-1010
[34]
Beyond TME Collaborative.
Consensus statement on the multidisciplinary management of patients with recurrent and primary rectal cancer beyond total mesorectal excision planes.
Br J Surg., 100 (2013), pp. E1-33
[35]
D.J. Lee, P.M. Sagar, G. Sadadcharam, K.Y. Tan.
Advances in surgical management for locally recurrent rectal cancer: how far have we come?.
World J Gastroenterol., 23 (2017), pp. 4170-4180
[36]
Y.N. You, J.M. Skibber, C.Y. Hu, et al.
Impact of multimodal therapy in locally recurrent rectal cancer.
Br J Surg, 103 (2016), pp. 753-762
[37]
PelvEx Collaborative.
Management strategies for patients with advanced rectal cancer and liver metastases using modified Delphi methodology: results from the PelvEx collaborative.
Colorectal Dis, 22 (2020), pp. 1184-1188
[38]
PelvEx Collaborative.
Simultaneous pelvic exenteration and liver resection for primary rectal cancer with synchronous liver metastases: results from the PelvEx Collaborative.
Colorectal Dis., 22 (2020), pp. 1258-1262
[39]
W.R. Grimes, C.J. Dunton, M. Stratton.
Pelvic Exenteration.
In: StatPearls [Internet], StatPearls Publishing, (2024),
[40]
P.A. Georgiou, P.P. Tekkis, V.A. Constantinides, et al.
Diagnostic accuracy and value of magnetic resonance imaging (MRI) in planning exenterative pelvic surgery for advanced colorectal cancer.
Eur J Cancer., 49 (2013), pp. 72-81
[41]
S.R. Kim, Y.Y. Lee, H. Brar, et al.
Utility of 18F-FDG-PET/CT imaging in patients with recurrent gynecological malignancies prior to pelvic exenteration.
Int J Gynecol Cancer., (2019),
[42]
C.S.H. Johnstone, D. Roberts, S. Mathieson, et al.
Pain, pain management and related outcomes following pelvic exenteration surgery: a systematic review.
Colorectal Dis., 25 (2023), pp. 562-572
[43]
S. Nougaret, D.M.J. Lambregts, G.L. Beets, et al.
Imaging in pelvic exenteration-a multidisciplinary practice guide from the ESGAR-SAR-ESUR-PelvEx collaborative group.
[44]
W.E. Brown, C.E. Koh, T. Badgery-Parker, M.J. Solomon.
Validation of MRI and surgical decision making to predict a complete resection in pelvic exenteration for recurrent rectal cancer.
Dis Colon Rectum, 60 (2017), pp. 144-151
[45]
A. Garcia-Granero, G. Pellino, F. Giner, et al.
A mathematical 3D-method applied to MRI to evaluate prostatic infiltration in advanced rectal cancer.
Tech Coloproctol., 24 (2020), pp. 605-607
[46]
N. Horvat, D.D.B. Bates, I. Petkovska.
Novel imaging techniques of rectal cancer: what do radiomics and radiogenomics have to offer? A literature review.
Abdom. Radiol., 44 (2019), pp. 3764-3774
[47]
I. Drami, A.C. Lord, P. Sarmah, et al.
Preoperative assessment and optimisation for pelvic exenteration in locally advanced and recurrent rectal cancer: a review.
Eur J Surg Oncol., 48 (2022), pp. 2250-2257
[48]
Y.Y.L. Johnson, M.M.A. West, L.E. Gould, et al.
Empty pelvis syndrome: a systematic review of reconstruction techniques and their associated complications.
Colorectal Dis., 24 (2021), pp. 16-26
[49]
P. Persson, P. Chong, C.W. Steele, M. Quinn.
Prevention and management of complications in pelvic exenteration.
Eur J Surg Oncol., 48 (2022), pp. 2277-2283
[50]
D.W. Hamilton, B. Heaven, R.G. Thomson, J. Wilson, C. Exley.
Multidisciplinary team decision-making in cancer and the absent patient: a qualitative study.
BMJ Open, 6 (2016),
[51]
S. Nordkamp, D.M.J. Creemers, S. Glazemakers, et al.
Implementation of an enhanced recovery after surgery protocol in advanced and recurrent rectal cancer patients after beyond total mesorectal excision surgery: a feasibility study.
Cancers (Basel)., 15 (2023),
[52]
L. Carballo, J.M. Enríquez-Navascués, Y. Saralegui, et al.
Total pelvic exenteration for the treatment of advanced primary or recurrent pelvic neoplasia.
Cir Esp., 93 (2015), pp. 174-180
[53]
C.A. Palma, C.S. van Kessel, M.J. Solomon, et al.
Bladder preservation or complete cystectomy during pelvic exenteration of patients with locally advanced or recurrent rectal cancer, what should we do?.
Eur J Surg Oncol, 49 (2023), pp. 1250-1257
[54]
R. Jaganmurugan, M. Kazi, V. Sukumar, et al.
Bladder preserving robotic pelvic exenteration for locally advanced rectal cancer-technique and short-term outcomes.
J Surg Oncol., (2022),
[55]
K.K.S. Austin, A.J. Herd, M.J. Solomon, K. Ly, P.J. Lee.
Outcomes of pelvic exenteration with en bloc partial or complete pubic bone excision for locally advanced primary or recurrent pelvic cancer.
Dis Colon Rectum, 59 (2016), pp. 831-835
[56]
M.J. Solomon, K.K. Austin, L. Masya, et al.
Pubic bone excision and perineal urethrectomy for radical anterior compartment excision during pelvic exenteration.
Dis Colon Rectum, 58 (2015), pp. 1114-1119
[57]
D.P. Harji, B. Griffiths, D.R. McArthur, P.M. Sagar.
Surgery for recurrent rectal cancer: higher and wider?.
Colorectal Dis., 15 (2013), pp. 139-145
[58]
M.J. Solomon, K.K. Tan, R.G. Bromilow, et al.
Sacrectomy via the abdominal approach during pelvic exenteration.
Dis Colon Rectum, 57 (2014), pp. 272-277
[59]
K.G. Brown, M.J. Solomon, K.K. Austin, et al.
Posterior high sacral segmental disconnection prior to anterior en bloc exenteration for recurrent rectal cancer.
Tech Coloproctol, 20 (2016), pp. 401-404
[60]
I. Shaikh, I. Holloway, W. Aston, Complex Cancer Clinic St Mark’s Hospital London, et al.
High subcortical sacrectomy: a novel approach to facilitate complete resection of locally advanced and recurrent rectal Cancer with high (S1-S2) sacral extension.
ColorectalDis., 18 (2016), pp. 386-392
[61]
T. Milne, M.J. Solomon, P. Lee, et al.
Assessing the impact of a sacral resection on morbidity and survival after extended radical surgery for locally recurrent rectal cancer.
Ann Surg, 258 (2013), pp. 1007-1013
[62]
A.C. Rogers, J.T. Jenkins, S. Rasheed, et al.
Towards standardisation of technique for en bloc sacrectomy for locally advanced and recurrent rectal cancer.
Clin Med, 10 (2021),
[63]
M.R. Fahy, C. Hayes, M.E. Kelly, D.C. Winter.
Updated systematic review of the approach to pelvic exenteration for locally advanced primary rectal cancer.
Eur J Surg Oncol., 48 (2022), pp. 2284-2291
[64]
Y.C. Lau, K. Jongerius, C. Wakeman, et al.
Influence of the level of sacrectomy on survival in patients with locally advanced and recurrent rectal cancer.
Br J Surg, 106 (2019), pp. 484-489
[65]
T. Milne, M.J. Solomon, P. Lee, et al.
Sacral resection with pelvic exenteration for advanced primary and recurrent pelvic cancer.
Dis Colon Rectum, 57 (2014), pp. 1153-1161
[66]
A. Sasikumar, C. Bhan, J.T. Jenkins, A. Antoniou, J. Murphy.
Systematic review of pelvic exenteration with En bloc sacrectomy for recurrent rectal adenocarcinoma: R0 resection predicts disease-free survival.
Dis Colon Rectum, 60 (2017), pp. 346-352
[67]
H.G. Moore, M. Shoup, E. Riedel, et al.
Colorectal cancer pelvic recurrences: determinants of Resectability.
Dis Colon Rectum, 47 (2004), pp. 1599-1606
[68]
K.K. Austin, M.J. Solomon.
Pelvic exenteration with en bloc iliac vessel resection for lateral pelvic wall involvement.
Dis Colon Rectum, 52 (2009), pp. 1223-1233
[69]
M. Movahedi, Z. Niakan, Z. Shahshahan, A.R. Hooshmand Meibodi, A. Babak, M. Saeidi.
Prophylactic hypogastric arterial ligation before cesarean hysterectomy for controlling complications in pregnant women with placenta adherent abnormality: a randomized controlled clinical trial.
J Res Med Sci., 27 (2022), pp. 63
[70]
M. Höckel.
Laterally extended endopelvic resection (LEER)--principles and practice.
Gynecol Oncol., 111 (2008), pp. S13-7
[71]
G.S. Choi, H.J. Kim.
The role of lateral pelvic lymph node dissection in advanced rectal cancer: a review of current evidence and outcomes.
Ann Coloproctol, 40 (2024), pp. 363-374
[72]
T. Xiao, J. Chen, Q. Liu.
Management of internal iliac and obturator lymph nodes in mid-low rectal cancer.
World J Surg Oncol., 22 (2024), pp. 153
[73]
T. Sammour.
The oncologic benefits of lateral lymph node dissection after neoadjuvant therapy - local control or survival?.
Tech Coloproctol., 29 (2025), pp. 51
[74]
S. Narihiro, et al.
Two-team lateral lymph node dissection assisted by the transanal approach for locally advanced lower rectal cancer: comparison with the conventional transabdominal approach.
SurgEndosc., 37 (2023), pp. 5256-5264
[75]
B. Glimelius.
Recurrent rectal cancer. The pre-irradiated primary tumour: can more radiotherapy be given?.
Colorectal Dis., 5 (2003), pp. 501-503
[76]
J. Lukovic, J.-M. Bourque, M. Abdel-Wahab.
A systematic review on the role for reirradiation in locally recurrent rectal cancer.
J Radiat Oncol., 4 (2015), pp. 141-148
[77]
R. Mirnezami, G.J. Chang, P. Das, et al.
Intraoperative radiotherapy in colorectal cancer: systematic review and meta-analysis of techniques, long-term outcomes, and complications.
Surg Oncol., 22 (2012), pp. 22-35
[78]
J.R. Hyngstrom, C.W. Tzeng, S. Beddar, et al.
Intraoperative radiation therapy for locally advanced primary and recurrent colorectal cancer: Ten-year institutional experience.
J Surg Oncol, 109 (2014), pp. 652-658
[79]
M.G. Haddock.
Intraoperative radiation therapy for colon and rectal cancers: a clinical review.
Radiat Oncol., 12 (2017), pp. 11
[80]
M. Nimer, F.G. Ali.
Use of intraoperative radiation therapy in rectal cancer.
Dis Colon Rectum., 67 (2024), pp. 1101-1105
[81]
R.J. Shine, T. Glyn, F. Frizelle.
Pelvic exenteration: a review of current issues/controversies.
ANZ J Surg., 92 (2022), pp. 2822-2828
[82]
A. Pilar, M. Gupta, S.G. Laskar, S. Laskar.
Intraoperative radiotherapy: review of techniques and results.
E Cancer med. Sci., 11 (2017), pp. 750
[83]
R.C. Dresen, M.J. Gosens, H. Martijn, et al.
Radical resection after IORT-containing multimodality treatment is the most important determinant for outcome in patients treated for locally recurrent rectal cancer.
Ann Surg Oncol., 15 (2008), pp. 1937-1947
[84]
M. Williams, M. Perera, F.X. Nouhaud, G. Coughlin.
Robotic pelvic exenteration and extended pelvic resections for locally advanced or synchronous rectal and urological malignancy.
Investig Clin Urol., 62 (2021), pp. 111-120
[85]
T.P. Chang, A.Y. Chok, D. Tan, et al.
The emerging role of robotics in pelvic exenteration surgery for locally advanced rectal cancer: a narrative review.
J Clin Med., 10 (2021),
[86]
M. Williams, M. Perera, F.-X. Nouhaud, G. Coughlin.
Robotic pelvic exenteration and extended pelvic resections for locally advanced or synchronous rectal and urological malignancy.
Investig Clin Urol., 62 (2021), pp. 111-120
[87]
O.K. Ryan, K.L. Doogan, ÉJ. Ryan, et al.
Comparing minimally invasive surgical and open approaches to pelvic exenteration for locally advanced or recurrent pelvic malignancies - Systematic review and meta-analysis.
Eur J Surg Oncol., 49 (2023), pp. 1362-1373
[88]
PelvEx Collaborative.
Minimally invasive surgery techniques in pelvic exenteration: a systematic and meta-analysis review.
SurgEndosc., 32 (2018), pp. 4707-4715
[89]
R.K. Lee, H. Abol-Enein, W. Artibani, et al.
Urinary diversion after radical cystectomy for bladder cancer: options, patient selection, and outcomes.
BJU Int, 113 (2014), pp. 11-23
[90]
M. Gachabayov, H. Lee, I. Tulina, et al.
Double-barreled wet colostomy versus separate urinary and fecal diversion in patients undergoing total pelvic exenteration: a cohort meta-analysis.
Surg Technol Int, 35 (2019), pp. 148-152
[91]
F.J. Backes, B.J. Tierney, E.L. Eisenhauer, et al.
Complications after double- barreled wet colostomy compared to separate urinary and fecal diversion during pelvic exenteration: time to change back?.
Gynecol Oncol, 128 (2013), pp. 60-64
[92]
H. Cholewa, J. Sancho-Muriel, B. Flor-Lorente.
Double-Barreled wet colostomy after pelvic exenteration.
Dis Colon Rectum., 67 (2024), pp. e13-e14
[93]
M. Jurado, A. Bazán, J.L. Alcázar, E. Garcia-Tutor.
Primary vaginal reconstruction at the time of pelvic exenteration for gynecologic cancer: morbidity revisited.
Ann Surg Oncol, 16 (2009), pp. 121-127
[94]
N. Griffin, J. Rabouhans, L.A. Grant, et al.
Pelvi-perineal flap reconstruction: Normal imaging appearances and post-operative complications on cross-sectional imaging.
Insights Imaging, 2 (2011), pp. 215-223
[95]
K.G.M. Brown, C.E. Koh, M.J. Solomon, Q. Qasabian, D. Robinson, S. Dubenec.
Outcomes after en bloc iliac vessel excision and reconstruction during pelvic exenteration.
Dis Colon Rectum, 58 (2015), pp. 850-856
[96]
O. Peacock, N. Smith, P.S. Waters, et al.
Preemptive femoral femoral crossover grafting of artery and vein before pelvic exenterative surgery for locally advanced and recurrent pelvic malignancy involving the aortoiliac axis.
Dis Colon Rectum, 64 (2020), pp. e2-e5
[97]
K. Komori, H. Suda, T. Kinoshita, Y. Sato, A. Ouchi, Y. Shimizu.
Resection of the external iliac artery with axillofemoral bypass for local recurrence of rectal cancer.
Tech Coloproctol, 25 (2021), pp. 1329-1331
[98]
C. Devulapalli, A.T. Jia Wei, J.R. DiBiagio, et al.
Primary versus flap closure of perineal defects following oncologic resection: a system atic review and meta-analysis.
Plast Reconstr Surg., 137 (2016), pp. 1602-1613
[99]
P. Lee, W.J. Tan, K.G.M. Brown, M.J. Solomon.
Addressing the empty pelvic syndrome following total pelvic exenteration: does mesh re construction help?.
Colorectal Dis., 21 (2019), pp. 365-369
[100]
P.W. Thomas, J.E.M. Blackwell, P.J.J. Herrod, et al.
Long-term outcomes of biological mesh repair following extra levator abdominoperineal excision of the rectum: an observational study of 100 patients.
Tech. Col oproctol, 23 (2019), pp. 761-767
[101]
Y. Lu, G. Chen, Z. Long, et al.
Novel 3D-printed prosthetic composite for reconstruction of massive bone defects in lower extremities after malignant tumour resection.
J Bone Oncol., 16 (2019),
[102]
M. Mori, A. Elsayem, S.K. Reddy, E. Bruera, N.A. Fadul.
Unrelieved pain and suffering in patients with advanced cancer.
Am J Hosp Palliat Med., 29 (2011), pp. 236-240
[103]
K.G.M. Brown, J. Pisaniello, K.S. Ng, et al.
Variation in outcome measurement and reporting in studies of pelvic exenteration for locally advanced and recurrent rectal cancer: a systematic review.
Colorectal Dis., 26 (2024), pp. 272-280
[104]
A. Lewandowska, S. Szubert, K. Koper, A. Koper, G. Cwynar, L. Wicherek.
Analysis of long-term outcomes in 44 patients following pelvic exenteration due to cervical cancer.
World J Surg Oncol., 18 (2020), pp. 234
[105]
A. Bogner, J. Fritzmann, B. Müssle, et al.
Pelvic exenteration for colorectal and non-colorectal cancer: a comparison of perioperative and oncological outcome.
Int J Colorectal Dis., 36 (2021), pp. 1701-1710
[106]
J. Maudsley, R.E. Clifford, O. Aziz, P.A. Sutton.
A systematic review of oncosurgical and quality of life outcomes following pelvic exenteration for locally advanced and recurrent rectal cancer.
Ann R Coll Surg Engl., (2024),
[107]
O. Peacock, P.S. Waters, J.C. Kong, et al.
Complications after extended radical resections for locally advanced and recurrent pelvic malignancies: a 25-year experience.
Ann Surg Oncol., 27 (2020), pp. 409-414
[108]
G.H. Ramshorst, J.M. Young, M.J. Solomon.
Complications and impact on quality of life of vertical rectus abdominis myocutaneous flaps for reconstruction in pelvic exenteration surgery.
Dis Colon Rectum, 63 (2020), pp. 1225-1233
[109]
P.A. Sutton, K.G.M. Brown, N. Ebrahimi, M.J. Solomon, K.K.S. Austin, P.J. Lee.
Long-term surgical complications following pelvic exenteration: operative management of the empty pelvis syndrome.
Colorectal Dis., 24 (2022), pp. 1491-1497
[110]
K.G. Brown, M.J. Solomon, E.R. Latif, et al.
Urological complications after cystectomy as part of pelvic exenteration are higher than that after cystectomy for primary bladder malignancy.
J Surg Oncol, 115 (2017), pp. 307-311
[111]
K. Harada, I. Sakai, M. Muramaki, et al.
Reconstruction of urinary tract combined with surgical management of locally advanced non-urological cancer involving the genitourinary organs.
Urol Int, 76 (2006), pp. 82-86
[112]
C.K. Pleth Nielsen, M.M. Sørensen, H.K. Christensen, J.A. Funder.
Complications and survival after total pelvic exenteration.
Eur J Surg Oncol., 48 (2022), pp. 1362-1367
[113]
K. Vuong, L.M. Alchin, M.J. Solomon, C.E. Koh, D. Steffens.
A prospective investigation of pain and fatigue following pelvic exenteration.
Eur J Surg Oncol., 47 (2021),
[114]
T.J. Miner, D.P. Jaques, P.B. Paty, J.G. Guillem, W.D. Wong.
Symptom control in patients with locally recurrent rectal cancer.
Ann Surg Oncol., 10 (2003), pp. 72-79
[115]
PelvEx Collaborative.
Beating the empty pelvis syndrome: the PelvEx Collaborative core outcome set study protocol.
BMJ Open., 14 (2024),
[116]
R.E. Jimenez, M. Shoup, A.M. Cohen, P.B. Paty, J. Guillem, D.W. Wong.
Contemporary outcomes of total pelvic exenteration in the treatment of colorectal cancer.
Dis Colon Rectum., (2003), pp. 46
[117]
Y.N. You, J.M. Skibber, C. Hu, et al.
Impact of multimodal therapy in locally recurrent rectal cancer.
Br J Surg, 103 (2016), pp. 753-762
[118]
C. Harris, M. Solomon, A.G. Heriot, et al.
The outcomes and patterns of treatment failure after surgery for locally recurrent rectal cancer.
Ann Surg, 264 (2016), pp. 323-329
[119]
D.P. Harji, P.M. Sagar, K. Boyle, et al.
Outcome of surgical resection of second-time locally recurrent rectal cancer.
Br J Surg, 100 (2013), pp. 403-409
[120]
D.T. Colibaseanu, K.L. Mathis, Z.M. Abdelsattar, et al.
Is curative resection and long-term survival possible for locally re-recurrent colorectal cancer in the pelvis?.
Dis Colon Rectum, 56 (2013), pp. 14-19
[121]
A. Esmailzadeh, M.S. Fakhari, N. Saedi, N. Shokouhi, A. Almasi-Hashiani.
A systematic review and meta-analysis on mortality rate following total pelvic exenteration in cancer patients.
BMC Cancer., 24 (2024), pp. 593
[122]
S.R. Miri, S. Akhavan, A.S. Mousavi, et al.
A systematic review on overall survival and disease-free survival following total pelvic exenteration.
Asian Pac J Cancer Prev., 23 (2022), pp. 1137-1145
[123]
PelvEx Collaborative.
Factors affecting outcomes following pelvic exenteration for locally recurrent rectal cancer.
Br J Surg., 105 (2018), pp. 650-657
[124]
D.P. Harji, B. Griffiths, G. Velikova, et al.
Systematic review of health-related quality of life in patients undergoing pelvic exenteration.
Eur J Surg Oncol, 42 (2016), pp. 1132-1145
[125]
A.S.E. McCarthy, M.J. Solomon, C.E. Koh, A. Firouzbakht, S.A. Jackson, D. Steffens.
Quality of life and functional outcomes following pelvic exenteration and sacrectomy.
Color. Dis., 22 (2020), pp. 521-528
[126]
J. Young, M. Solomon, D. Steffens, C. Koh.
Long-term consequences of exenterative surgery for people with pelvic cancer.
J Clin Oncol, 36 (2018), pp. 118

CURRENT ADDRESS: Avinguda de Fernando Abril Martorell, 106, Quatre Carreres, 46026 València, Hospital Universitario y Politécnico La Fe, Torre G, planta 5, Coloproctology Unit. General and Digestive System Surgery Department.

asdasdasd
Article options
Tools