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Vol. 92. Issue 4.
Pages 277-282 (April 2014)
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Vol. 92. Issue 4.
Pages 277-282 (April 2014)
Original article
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Resected Non-Small Cell Bronchogenic Carcinoma Stage pIIIA-N2. Which Patients Will Benefit Most From Adjuvant Therapy?
Carcinoma broncogénico no microcítico resecado, estadio pIIIA-N2. ¿En qué pacientes la adyuvancia ofrece mayor beneficio?
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Ana M. Gómeza,
Corresponding author
agm912@hotmail.com

Corresponding author.
, José Ramón Jaraboa, Cristina Fernandezb, Joaquín Calatayuda, Elena Fernándeza, Antonio J. Torresa, José L. Balibreaa, Florentino Hernandoa, the Bronchogenic Carcinoma Cooperative Group of the Spanish Society of Pneumology and Thoracic Surgery (GCCB-SEPAR)
a Servicio de Cirugía General II y Cirugía Torácica, Hospital Clínico San Carlos, Madrid, Spain
b Servicio de Medicina Preventiva, Hospital Clínico San Carlos, Madrid, Spain
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Table 1. Descriptive Data of the Series.
Table 2. Surgical Data of the Series.
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Abstract
Background

Controversy persists as regards the indications and results of surgery in the treatment of patients with stage pIIIA-N2 non-small cell lung cancer (NSCLC). The objective of this study was to analyze the overall survival of a multicenter series of these patients and the role of adjuvant treatment, looking for factors that may define subgroups of patients with an increased benefit from this treatment.

Methods

A retrospective study was conducted on 287 patients, with stage pIIIA-N2 NSCLC subjected to complete resection, taken from a multi-institutional database of 2994 prospectively collected consecutive patients who underwent surgery for lung cancer. Adjuvant treatment was administered in 238 cases (82.9%). Analyses were made of the age, gender, histological type, administration of induction and adjuvant chemotherapy and/or radiation therapy treatments.

Results

The 5-year survival was 24%, with a median survival of 22 months. Survival was 26.5% among patients receiving with adjuvant treatment, versus 10.7% for those without it (P=.069). Age modified the effect of adjuvant treatment on survival (interaction P=.049). In patients under 70 years of age with squamous cell carcinoma, adjuvant treatment reduced the mortality rate by 37% (hazard ratio: 0.63; 95% CI; 0.42–0.95; P=.036).

Conclusions

Completely resected patients with stage pIIIA-N2 NSCLC receiving adjuvant treatment reached higher survival rates than those who did not. Maximum benefit was achieved by the subgroup of patients under 70 years of age with squamous cell carcinoma.

Keywords:
Stage IIIA
N2
Lung cancer
Surgery
Survival
Adjuvant treatment
Resumen
Introducción

Las indicaciones y resultados de la cirugía en el tratamiento de pacientes con carcinoma broncogénico no microcítico (CBNM) en estadio IIIA-N2 continúa siendo objeto de debate. Este estudio analiza la supervivencia global y el papel del tratamiento adyuvante en una serie multicéntrica de pacientes en estadio IIIA-N2 completamente resecados, buscando factores que puedan definir subgrupos de pacientes en quienes esta adyuvancia resulte más beneficiosa.

Material y métodos

Estudio retrospectivo de una serie multicéntrica de pacientes con CBNM resecado en estadio IIIA por N2 tomados de una base de datos con 2.994 pacientes intervenidos por CBNM recogidos prospectivamente. Se estudia la supervivencia y la influencia de las variables edad, género, tipo histológico y administración de tratamiento neoadyuvante y coadyuvante con quimioterapia o radioterapia.

Resultados

La supervivencia global de la serie a 5 años fue del 24% con una supervivencia media de 22 meses. En pacientes con tratamiento adyuvante fue de 26,5%, contra un 10,7% en aquellos sin adyuvancia (p=0,069). La edad modificó el efecto de la adyuvancia (interacción p=0,049). En pacientes por debajo de 70 años con carcinoma epidermoide, el tratamiento adyuvante redujo la tasa de mortalidad un 37% (hazard ratio: 0,63; p=0,036).

Conclusiones

El tratamiento adyuvante aumentó la supervivencia en los pacientes con CBNM resecado en estadio IIIA-N2. El beneficio fue mayor en pacientes de menos de 70 años con carcinoma epidermoide.

Palabras clave:
Estadio IIIA
N2
Cáncer de pulmón
Cirugía
Supervivencia
Adyuvancia
Full Text
Introduction

Up to 80% of lung neoplasms are non-small-cell lung cancer (NSCLC). Approximately 15% are found in stage IIIA-N2 at diagnosis,1 meaning that they have ipsilateral mediastinal lymph node involvement. However, it is a very heterogenous group of patients whose treatment is still the object of debate.2–4 It is still not clear which patients will benefit from surgical resection. Many studies have tried to identify prognostic factors in this stage. What seems to be becoming more and more evident is that it is a disease that requires multidisciplinary treatment in most cases.5 The objective of this study is to analyze overall survival in a multicenter study of patients with NSCLC and resected N2 mediastinal disease, and to determine the role of adjuvant treatment while analyzing whether there is a subgroup of patients in whom adjuvant therapy was significantly more beneficial.

Materials and Methods

This is an observational, retrospective, multicenter study of patients with NSCLC in surgical-pathological stage IIIA-N2 that had been completely resected. The cases came from a database of 2994 patients who underwent surgery for lung cancer at hospitals belonging to the Bronchogenic Carcinoma Workgroup of the Spanish Society of Pulmonology and Thoracic Surgery (in Spanish, GCCB-SEPAR) between October 1993 and September 1997.6 These patients represent approximately 50% of the cases with these characteristics in Spain during this time period. Although the hospitals were of different types, the surgical and oncologic aspects were homogeneous.7 The data collection process underwent a strict quality control to ensure the reliability and homogeneity of the determinations.8 The study was approved by the Ethics Committee of the coordinating hospital center. Staging was done in accordance with the TNM classification for NSCLC published in 1997.1 Induction chemotherapy was indicated in patients with histologic confirmation of N2 mediastinal lymph node involvement. In all the cases analyzed, the resection was complete, meaning that there were tumor-free resection margins, no extracapsular extension of the lymph nodes, no involvement of the most cranial or most caudal lymph node stations analyzed, and cytology confirmation negative for malignancy in the cases with associated pleural effusion.9 For our study, we selected the 319 cases with N2 post-op pathology diagnosis, in other words, patients with resected N2 disease. We excluded the 32 patients who died during the post-op period (either in hospital or within the first 30 days after resection). The remaining 287 patients made up the final sample of our study. The patients were followed up in the outpatient setting for more than 5 years with thoracoabdominal computed tomography (CT) at least every 6 months. The following variables were analyzed: sex, age (in 2 age groups: younger than 70, or 70 and older), histology, resection type and adjuvant treatment (chemotherapy or radiotherapy and time of administration). The qualitative variables are shown in their distribution of frequencies, and the quantitative variables as mean with standard deviation or as mean and interquartile range. For the survival analysis, the Kaplan–Meier method was used. For the analysis of the possible impact on survival of the different variables, the Cox proportional hazards model was used. The hazard ratios (HR) are presented with a 95% confidence interval (95% CI). The statistical study was performed with the SPSS 15.0 program (IBM Systems, Chicago, United States).

Results

The total number of patients who met the inclusion criteria was 287. The average follow-up period was 92 months (range 66–113), meaning that the patients were followed for more than 5 years, which was one of the initial conditions of the study. The basic characteristics of the patients are detailed in Table 1. The types of surgical resection performed are detailed in Table 2. In all cases, systematic mediastinal lymph node dissection, systematic lymph node sampling or lobe-specific lymph node samplings were performed.

Table 1.

Descriptive Data of the Series.

Variable  Value (n=287) 
Mean age  61.4 (range 37–81) 
Under 70  215 (75%) 
70 or older  72 (25%) 
Sex
Males  266 (93.7%) 
Female  21 (6.3%) 
Histology
Squamous  166 (57.8%) 
Adenocarcinoma  88 (30.7%) 
Bronchioloalveolar  4 (1.4%) 
Undifferentiated large-cell  18 (6.3%) 
Other  11 (3.8%) 
Adjuvants
Neoadjuvant CTx  18 (6%) 
Post-operative CTx  78 (27.2%) 
Post-operative RTx  65 (22.6%) 
Postoperative CRT  95 (33.1%) 
No postoperative adjuvant treatment  49 (17.1%) 

CRT: chemoradiotherapy; CTx: chemotherapy; RTx: radiotherapy.

Table 2.

Surgical Data of the Series.

Type of resection  Number of patients (n=287) 
Pneumonectomy  134 (46.7%) 
Left  79 
Right  55 
Bilobectomy  15 (5.2%) 
Lobectomy  115 (40.1%) 
Segmental resection  23 (8%) 

The actuarial survival estimated by applying the Kaplan–Meier method for the entire series of 287 patients at 12, 24, 36, 48 and 60 months was 71%, 48%, 36%, 30%, and 24%, respectively.

Among the 238 patients who were administered postoperative adjuvant treatment (83% of the total series), the actuarial survival estimated at 12, 24, 36, 48, and 60 months was 72%, 49%, 39%, 32%, and 26%, respectively. The survival rates were greater than those of the patients who did not receive adjuvant therapy (61%, 42%, 22%, 13%, and 11%). These differences did not reach statistical significance, although they did show a clear trend (P=.069) (Fig. 1).

Fig. 1.

Survival curves of the series of those patients who either received postoperative adjuvant treatment or not. The survival of patients who received adjuvant therapy was longer, although without reaching a significant difference (P=.069).

(0.11MB).

When histology was analyzed, the difference in survival in favor of the patients who received adjuvant treatment was significant when the tumor was squamous-cell carcinoma. Thus, among the 113 cases of epidermoid carcinoma, survival at 12, 24, 36, 48 and 60 months was 67%, 47%, 37%, 29%, and 24%, respectively, for those who received adjuvant therapy, and 52%, 31%, 10%, 7%, and 7%, respectively, for those who did not (P=.02) (Fig. 2).

Fig. 2.

Survival curves of the series according to adjuvant treatment in patients with epidermoid carcinoma. The differences in favor of adjuvant treatment reached statistical significance (P=.02).

(0.06MB).

In patients with NSCLC with non-squamous histology, these differences disappear (75%, 59%, 29%, 23%, and 18% vs 74%, 49%, 40%, 35%, and 28%–with and without adjuvant treatment, respectively).

There were no differences in survival with respect to sex. However, when classified by age with the arbitrary cut-off of 70, we found that the effect of adjuvant therapy seems to be influenced by this variable.

Thus, in patients under the age of 70, the actuarial survival at 12, 24, 36, 48 and 60 months was 50%, 35%, 25%, 21%, and 19%, which ascends to 77%, 55%, 44%, 36%, and 30%, respectively, in patients who received adjuvant treatment. In contrast, the patients aged 70 or older who did not receive adjuvancy presented higher survival rates, although this finding was not significant.

The Cox proportional hazards analysis demonstrates that, in patients under the age of 70 with epidermoid NSCLC, adjuvant treatment reduces the mortality rate by 37% (HR: 0.63; 95% CI: 0.42–0.95). This result is statistically significant (P=.036) (Fig. 3).

Fig. 3.

Role of adjuvant therapy in the survival of patients under the age of 70 with epidermoid carcinoma: the variable acts as a protective factor against mortality (P=.036).

(0.08MB).
Discussion

The overall 5-year survival for patients with NSCLC in stage IIIA due to ipsilateral mediastinal lymph node involvement (N2) ranges from 15% to 30%. These rates have hardly changed in the last 20 years.4,10,11

A recent European survey of thoracic surgeons demonstrated the heterogeneity of NSCLC in stage IIIA-N2. While 50% of survey participants were in favor of neoadjuvant therapy and a subsequent proposal of surgical resection, almost one-third opted directly for definitive chemo-radiotherapy treatment. And a significant group of those surveyed would proceed directly to surgical resection. The most recent edition of the clinical practice guidelines published by the American College of Chest Physicians (ACCP) indicates that “In patients with discrete N2 involvement by NSCLC identified preoperatively (IIIA), primary surgical resection followed by adjuvant therapy is not recommended (except as part of a clinical trial),” and that the standard treatment is chemo-radiotherapy.12 In addition, the only two randomized clinical trials published to date, the European Organization for Research and Treatment of Cancer-Lung Cancer Group (EORTC) and the Radiation Therapy Oncology Group (RTOG), do not support surgical treatment in N2.13,14 Nevertheless, it is becoming clearer that there are patient subgroups with favorable factors (patient-related as well as tumor-related) that can benefit from multidisciplinary treatment including surgery in N2.15,16 The clinical guidelines of the ACCP classifies N2 disease into 4 groups: 1) incidental N2, which is detected in the histopathology study after surgical resection; 2) incidental N2, found intraoperatively; 3) pre-operative N2 with histologic confirmation; and 4) multiple/bulky N2.12

This classification is frequently reduced to patients with pre-operatively discovered N2 and those with “incidental N2”, or those cases that are found in the pathology studies after resection.17,18 But it seems that heterogeneity also has an influence, to the point that the type of lymph node tumor involvement (extracapsular or not) or the number of affected lymph nodes or regions play an important role in the prognosis of these patients.19,20 One cannot forget that the surgery variable in this type of studies, meaning the type of lymph node dissection used, also defines the precision of patient staging.21,22

Most consensuses propose adjuvant treatment with chemotherapy or radiotherapy in patients with resected NSCLC in stage IIIA-N2.23–26

Adjuvant radiotherapy has been shown to reduce both locoregional and distant recurrences, together with an overall increase in survival.25,27 This benefit is clearer when the involvement is single station.28

With regards to adjuvant chemotherapy after complete surgical resection, some randomized studies have demonstrated that platin-based treatment increases survival.29 Douillard and Rosell30 found in the ANITA study an increase in 5-year survival, 19% in the group without treatment and 40% in the group with adjuvant therapy. These high rates, compared with our study, may be related with a lower percentage of pneumonectomies in the ANITA study (38% vs 47%). In addition, they established the cut-off age for the comparative study at 55 instead of 70, which was the cut-off age in our article. The meta-analysis performed by the LACE workgroup shows a reduction in the risk of mortality between 17% and 20% with adjuvant chemotherapy treatment based on cisplatin.31

Even though adjuvant chemotherapy in resected N2 patients is accepted, it is not clear whether the combination with radiotherapy can improve results in terms of survival and recurrence-free interval.32–35

The most recent meta-analysis analyzing the role of adjuvant chemotherapy in completely resected stage N2 CPNM demonstrates an increase of 4% in the 5-year survival (HR 0.86; 95% CI: 0.81–0.92).

Even with all the limitations of a retrospective study, our series shows that the patients who received adjuvant therapy after surgical resection presented longer survival rates than those who did not, although the difference was not significant. It demonstrates that the role of adjuvant therapy was significant among patients under the age of 70 with epidermoid carcinomas, with a reduction of 37% in the 5-year mortality rate (P=.036), adjusting the remaining variables with the Cox proportional hazard model.

In spite of the fact that it is a series with a rather significant number of patients for a national study (n=283), it presents the limitations of the studies in patients with CPNM in stage IIIA due to N2, which is its own heterogeneity. Thus, the causes for which the group without treatment did not receive adjuvant therapy are not homogenous. Likewise, the series has a high percentage of pneumonectomies, which itself is a factor that could bias the results.

In conclusion, in our series of patients who had complete stage N2 CPNM resection, adjuvant treatment was associated with increased overall survival, which was significant only in patients under the age of 70 who presented epidermoid carcinoma.

The confirmation of these data in a prospective study might question the indication for adjuvant treatment in patients over the age of 70, and especially those with non-epidermoid histology, in whom the benefits of this therapy are less clear.

Conflict of Interests

The authors have no conflict of interests to declare.

Addendum 1
Coordinators

José Luis Duque (Hospital Universitario, Valladolid); Angel López Encuentra, (Hospital Universitario 12 de Octubre, Madrid); Ramón Rami Porta, (Hospital Mutua de Terrassa, Barcelona).

Addendum 2
Local Representatives

Julio Astudillo (Hospital Germans Trias i Pujol, Barcelona); Josep Maria Gimferrer (Hospital Clinic, Barcelona); Antonio Cantó (Hospital Clínico, Valencia); Juan Casanova (Hospital de Cruces, Bilbao); Jorge Cerezal (Hospital Universitario, Valladolid); Antonio Fernández de Rota (Hospital Carlos Haya, Málaga); Federico González Aragoneses (Hospital Gregorio Marañón, Madrid); Jorge Freixinet (Hospital Nuestra Señora del Pino, Las Palmas); Nicolás Llobregat (Hospital Universitario del Aire, Madrid); Nuria Mañes (Fundación Jiménez Díaz, Madrid); Miguel Mateu (Hospital Mutua de Terrassa, Barcelona); José Luis Martín de Nicolás (Hospital Universitario 12 de Octubre, Madrid); Nuria Novoa (Complejo Hospitalario, Salamanca); Jesús Rodríguez (Complejo Hospitalario, Oviedo); Antonio José Torres García (Hospital Universitario San Carlos, Madrid); Mercedes de la Torre (Hospital Juan Canalejo, La Coruña); Abel Sánchez-Palencia (Hospital Virgen de las Nieves, Granada); Andrés Varela Ugarte (Clínica Puerta de Hierro, Madrid); Yat Wah Pun (Hospital de la Princesa, Madrid).

References
[1]
C.F. Mountain.
Revisions in the international system for staging lung cancer.
Chest, 111 (1997), pp. 1710-1717
[2]
G. Rocco.
Results of cutting-edge surgery in stage IIIA-N2 nonsmall cell lung cancer.
Curr Opin Oncol, 21 (2009), pp. 105-109
[3]
G. Rocco, F. Perrone, A. Rossi, C. Gridelli.
Surgical management of non-small cell lung cancer with mediastinal lymphadenopathy.
Clin Oncol (R Coll Radiol), 22 (2010), pp. 325-333
[4]
K. Chansky, J.P. Sculier, J.J. Crowley, D. Giroux, J. van Meerbeeck, P. Goldstraw.
The International Association for the Study of Lung Cancer Staging Project: prognostic factors and pathologic TNM stage in surgically managed non-small cell lung cancer.
J Thorac Oncol, 4 (2009), pp. 792-801
[5]
M. Bakir, S. Fraser, T. Routledge, M. Scarci.
Is surgery indicated in patients with stage IIIa lung cancer and mediastinal nodal involvement?.
Interact Cardiovasc Thorac Surg, 13 (2011), pp. 303-310
[6]
The surgery of bronchogenic carcinoma in, Spain, A., descriptive, study. The Cooperative Group on Bronchogenic Carcinoma of SEPAR., (GCCB-S).
Sociedad Española de Neumología y Cirugía Torácica.
Arch Bronconeumol, 31 (1995), pp. 303-309
[7]
A. Lopez Encuentra.
Criteria of functional and oncological operability in surgery for lung cancer: a multicenter study. The Bronchogenic Carcinoma Cooperative Group of the Spanish Society of Pneumology and Thoracic Surgery (GCCB-S).
Lung Cancer, 20 (1998), pp. 161-168
[8]
Grupo Cooperativo de Carcinoma Broncogénico de SEPAR (GCCB-S).
Control de calidad en un registro multiinstitucional de carcinoma broncogénico.
Arch Bronconeumol, 32 (1996), pp. S70
[9]
R. Rami-Porta, M. Mateu-Navarro, J. Freixinet, M. de la Torre, A.J. Torres-Garcia, Y.W. Pun, et al.
Type of resection and prognosis in lung cancer. Experience of a multicentre study.
Eur J Cardiothorac Surg, 28 (2005), pp. 622-628
[10]
N. Martini, B.J. Flehinger.
The role of surgery in N2 lung cancer.
Surg Clin North Am, 67 (1987), pp. 1037-1049
[11]
J.F. Vansteenkiste, P.R. de Leyn, G.J. Deneffe, T.E. Lerut, M.G. Demedts.
Clinical prognostic factors in surgically treated stage IIIA-N2 non-small cell lung cancer: analysis of the literature.
Lung Cancer, 19 (1998), pp. 3-13
[12]
L.A. Robinson, J.C. Ruckdeschel, H. Wagner Jr., C.W. Stevens.
Treatment of non-small cell lung cancer-stage IIIA: ACCP evidence-based clinical practice guidelines (2nd edition).
Chest, 132 (2007), pp. 243S-265S
[13]
K.S. Albain, R.S. Swann, V.W. Rusch, A.T. Turrisi 3rd, F.A. Shepherd, C. Smith, et al.
Radiotherapy plus chemotherapy with or without surgical resection for stage III non-small-cell lung cancer: a phase III randomised controlled trial.
[14]
J. Vansteenkiste, D. Betticher, W. Eberhardt, P. de Leyn.
Randomized controlled trial of resection versus radiotherapy after induction chemotherapy in stage IIIA-N2 non-small cell lung cancer.
J Thorac Oncol, 2 (2007), pp. 684-685
[15]
P. Garrido, J.L. Gonzalez-Larriba, A. Insa, M. Provencio, A. Torres, D. Isla, et al.
Long-term survival associated with complete resection after induction chemotherapy in stage IIIA (N2) and IIIB (T4N0-1) non small-cell lung cancer patients: the Spanish Lung Cancer Group Trial 9901.
J Clin Oncol, 25 (2007), pp. 4736-4742
[16]
J.A. Roth, F. Fossella, R. Komaki, M.B. Ryan, J.B. Putnam Jr., J.S. Lee, et al.
A randomized trial comparing perioperative chemotherapy and surgery with surgery alone in resectable stage IIIA non-small-cell lung cancer.
J Natl Cancer Inst, 86 (1994), pp. 673-680
[17]
C. Casali, A. Stefani, P. Natali, G. Rossi, U. Morandi.
Prognostic factors in surgically resected N2 non-small cell lung cancer: the importance of patterns of mediastinal lymph nodes metastases.
Eur J Cardiothorac Surg, 28 (2005), pp. 33-38
[18]
J.P. Van Meerbeeck, V.F. Surmont.
Stage IIIA-N2 NSCLC: a review of its treatment approaches and future developments.
Lung Cancer, 65 (2009), pp. 257-267
[19]
J.G. Lee, C.Y. Lee, I.K. Park, D.J. Kim, S.H. Cho, K.D. Kim, et al.
The prognostic significance of multiple station N2 in patients with surgically resected stage IIIA N2 non-small cell lung cancer.
J Korean Med Sci, 23 (2008), pp. 604-608
[20]
G.B. Ratto, R. Costa, P. Maineri, A. Alloisio, P. Bruzzi, B. Dozin.
Is there a subset of patients with preoperatively diagnosed N2 non-small cell lung cancer who might benefit from surgical resection?.
J Thorac Cardiovasc Surg, 138 (2009), pp. 849-858
[21]
N. Ilic, A. Petricevic, D. Arar, S. Kotarac, J. Banovic, N.F. Ilic, et al.
Skip mediastinal nodal metastases in the IIIa/N2 non-small cell lung cancer.
J Thorac Oncol, 2 (2007), pp. 1018-1021
[22]
W. Zhong, X. Yang, J. Bai, J. Yang, C. Manegold, Y. Wu.
Complete mediastinal lymphadenectomy: the core component of the multidisciplinary therapy in resectable non-small cell lung cancer.
Eur J Cardiothorac Surg, 34 (2008), pp. 187-195
[23]
P. Goldstraw, G.C. Mannam, D.K. Kaplan, P. Michail.
Surgical management of non-small-cell lung cancer with ipsilateral mediastinal node metastasis (N2 disease).
J Thorac Cardiovasc Surg, 107 (1994), pp. 19-27
[24]
J.F. Regnard, P. Magdeleinat, D. Azoulay, P. Dartevelle, M. Deneuville, A. Rojas-Miranda, et al.
Results of resection for bronchogenic carcinoma with mediastinal lymph node metastases in selected patients.
Eur J Cardiothorac Surg, 5 (1991), pp. 583-586
[25]
M. Debevec, M. Bitenc, S. Vidmar, T. Rott, J. Orel, P. Strojan, et al.
Postoperative radiotherapy for radically resected N2 non-small-cell lung cancer (NSCLC): randomised clinical study 1988–1992.
Lung Cancer, 14 (1996), pp. 99-107
[26]
K. Kim, E.K. Chie, J.Y. Jang, S.W. Kim, D.Y. Oh, S.A. Im, et al.
Role of adjuvant chemoradiotherapy for ampulla of Vater cancer.
Int J Radiat Oncol Biol Phys, 75 (2009), pp. 436-441
[27]
S.M. Keller, S. Adak, H. Wagner, A. Herskovic, R. Komaki, B.J. Brooks, et al.
A randomized trial of postoperative adjuvant therapy in patients with completely resected stage II or IIIA non-small-cell lung cancer. Eastern Cooperative Oncology Group.
N Engl J Med, 343 (2000), pp. 1217-1222
[28]
M.F. Jimenez, G. Varela, N.M. Novoa, J.L. Aranda.
Results of surgery for non-small cell lung cancer with N2 involvement unsuspected before thoracotomy.
Arch Bronconeumol, 44 (2008), pp. 65-69
[29]
K.M. Pisters, W.K. Evans, C.G. Azzoli, M.G. Kris, C.A. Smith, C.E. Desch, et al.
Cancer Care Ontario and American Society of Clinical Oncology adjuvant chemotherapy and adjuvant radiation therapy for stages I-IIIA resectable non small-cell lung cancer guideline.
J Clin Oncol, 25 (2007), pp. 5506-5518
[30]
J.Y. Douillard, R. Rosell, M. de Lena, F. Carpagnano, R. Ramlau, J.L. Gonzales-Larriba, et al.
Adjuvant vinorelbine plus cisplatin versus observation in patients with completely resected stage IB-IIIA non-small-cell lung cancer (Adjuvant Navelbine International Trialist Association [ANITA]): a randomised controlled trial.
Lancet Oncol, 7 (2006), pp. 719-727
[31]
J.P. Pignon, H. Tribodet, G.V. Scagliotti, J.Y. Douillard, F.A. Shepherd, R.J. Stephens, et al.
Lung adjuvant cisplatin evaluation: a pooled analysis by the LACE Collaborative Group.
J Clin Oncol, 26 (2008), pp. 3552-3559
[32]
B. Zou, Y. Xu, T. Li, W. Li, B. Tang, L. Zhou, et al.
A multicenter retrospective analysis of survival outcome following postoperative chemoradiotherapy in non-small-cell lung cancer patients with N2 nodal disease.
Int J Radiat Oncol Biol Phys, 77 (2010), pp. 321-328
[33]
H.A. Wakelee, P. Stephenson, S.M. Keller, H. Wagner, A. Herskovic, R. Komaki, et al.
Post-operative radiotherapy (PORT) or chemoradiotherapy (CPORT) following resection of stages II and IIIA non-small cell lung cancer (NSCLC) does not increase the expected risk of death from intercurrent disease (DID) in Eastern Cooperative Oncology Group (ECOG) trial E3590.
Lung Cancer, 48 (2005), pp. 389-397
[34]
J. Vansteenkiste, C. Dooms, P. de Leyn.
The multidisciplinarity of stage III non-small cell lung cancer.
Eur J Cancer, 45 (2009), pp. 92-105
[35]
R.J. Cerfolio, A.S. Bryant.
Survival of patients with unsuspected N2 (stage IIIA) nonsmall-cell lung cancer.
Ann Thorac Surg, 86 (2008), pp. 362-366

The names of the members of the Bronchogenic Carcinoma Cooperative Group of the Spanish Society of Pneumology and Thoracic Surgery (CBAG-SEPAR) listed in Addendums 1 and 2.

Please cite this article as: Gómez AM, Jarabo JR, Fernandez C, Calatayud J, Fernández E, Torres AJ, et al. Carcinoma broncogénico no microcítico resecado, estadio pIIIA-N2. ¿En qué pacientes la adyuvancia ofrece mayor beneficio? Cir Esp. 2014;92:277–282.

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