Concurrent cisplatin/etoposide plus 3D-conformal radiotherapy followed by surgery for stage IIB (superior sulcus T3N0)/III non-small cell lung cancer yields a high rate of pathological complete response

被引:40
|
作者
Pourel, Nicolas [1 ]
Santelmo, Nicola [3 ]
Naafa, Nidal [3 ]
Serre, Antoine [1 ]
Hilgers, Werner [2 ]
Mineur, Laurent [1 ]
Molinari, Nicolas [4 ]
Reboul, Francois [1 ]
机构
[1] Inst St Catherine, Dept Radiat Oncol, F-84082 Avignon 2, France
[2] Inst St Catherine, Dept Med Oncol, F-84082 Avignon, France
[3] Ctr Hosp Henri Duffaut, Dept Thorac Surg, Avignon, France
[4] Univ Montpellier, CHU Nimes, Serv DIM, Fac Med,Lab Biostat, Montpellier, France
关键词
induction; chemoradiation; surgery; non-small cell lung cancer; combined modality treatment;
D O I
10.1016/j.ejcts.2008.01.063
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction: Optimal preoperative treatment of stage IIB (Pancoast)/III non-small cell lung cancer (NSCLC) remains undetermined and a subject of controversy. The goat of our study is to confirm feasibility and pathological response rates after induction chemoradiation (CRT) in our community-based treatment center. Patients and methods: Patients were selected according to functional and resectability criteria. Induction treatment comprised 3D conformal 4500 cGy radiotherapy delivered to the primary tumor and pathologic hilar and/or mediastinal lymph nodes on CTscan with an extra-margin of 1-1.5 cm. Concurrent chemotherapy regimen was cisplatinum 20 mg/m(2) d1-d5 and etoposide 50 mg/m(2) d1-d5, d1-5 d29-33. Within 3-4 weeks after CRT completion, operability was re-assessed accordingly. Surgery was performed 4-6 weeks after CRT completion in patients (pts) deemed resectable. Inoperable pts were referred for a 20-25 Gy boost +/- 1 extra-cycle of cisplatinum + etoposide. Results: From 1996 to 2005, 107 pts were initially selected for treatment and received induction chemoradiation (stage IIB-Pancoast 18, IIIA 58 and IIIB 31, squamous cell carcinoma 48%, adenocarcinoma 44%, large-cell undifferentiated carcinoma 14%). After preoperative evaluation, 72 pts (67%) had a thoracotomy (pneumonectomy 21, lobectomy 45, bilobectomy 5) and all but one (unresectable tumor) had a macroscopic complete resection. During the 3-month postoperative time, five patients (6.9%) died, four after pneumonectomy (right 3, left 1). The analysis of tumoral samples showed a pathological complete response rate or microscopic residual foci of 39.5%. Median follow-up time was 22.3 months (survivors: 36.8 months), 2-year and 3-year overall survival rates were 55% and 40%, respectively (median = 26.7 months) for all the intention-to-treat population (n = 107), 62% and 51% (median = 36.5 months) for 71 resected pts, 41% and 16% for 36 non-resected pts (median = 19.1 months). On multivariate analysis, surgical resection and tumoral necrosis >50% (or pathological complete response) were the most pertinent predictive factors of the risk of death (hazard ratio = 0.50 and 0.48, p = 0.006 and 0.038, respectively). Conclusion: Surgery was feasible after induction chemoradiation, particularly lobectomy in PS 0-1, stage IIB (Pancoast)/III NSCLC pts but pneumonectomy carries a high risk of postoperative death (particularly, right pneumonectomy). Pathological response to induction chemoradiation was complete in 39.5% of patients and was a significant predictive factor of overall survival. (C) 2008 European Association for Cardio-Thoracic Surgery. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:829 / 836
页数:8
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