Induction chemotherapy followed by concurrent chemoradiation for patients with non-operable stage III non-small-cell lung cancer

被引:8
作者
Iranzo, Vega [1 ]
Bremnes, Roy M. [2 ]
Almendros, Piedad [3 ]
Gavila, Joaquin [1 ]
Blasco, Ana [1 ]
Sirera, Rafael [1 ,4 ]
Camps, Carlos [1 ,4 ]
机构
[1] Hosp Gen Univ, Med Oncol Serv, Valencia 46014, Spain
[2] Univ Tromso, Fac Med, Inst Clin Med, N-9001 Tromso, Norway
[3] Hosp Gen Univ, ERESA, Serv Radioterapia, Valencia 46014, Spain
[4] Fdn Hosp Gen Univ Valencia, Oncol Mol Lab, Valencia, Spain
关键词
Non-small-cell lung cancer; Stage III; Chemoradiotherapy; Radiotherapy; Chemotherapy; Concurrent; Sequential; COOPERATIVE-ONCOLOGY-GROUP; THORACIC RADIATION-THERAPY; COMBINED-MODALITY THERAPY; RANDOMIZED PHASE-II; LEUKEMIA GROUP-B; COMBINED CHEMORADIOTHERAPY; WEEKLY PACLITAXEL; RADIOTHERAPY; TRIAL; METAANALYSIS;
D O I
10.1016/j.lungcan.2008.04.016
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Combined modality treatment with chemotherapy (CT) and radiotherapy (RT) in stage III non-small-cell lung cancer is considered as standard therapy. As concomitant CT appears to be beneficial, the choice of anticancer agents and the role of induction chemotherapy is still unresolved. We present our experience based on an induction CT scheme with carboplatin plus paclitaxel followed by RT and concomitant CT. 31 patients with non-operable stage IIIA or IIIB NSCLC without pleural effusion were included in this study: 30 males, 1 female; median age 66 years (range: 50-81); 32% with non-operable stage IIIA and 68% with stage IIIB without pleural effusion: 61% squamous cell carcinoma, 32% adenocarcinoma and 7% other histologies. Regarding performance status (PS), 9.7% PS 0 and 90% PS 1 were included. Patients received 3 courses of induction CT with carboplatin AUC = 6 and paclitaxel 175 mg/m(2), administrated i.v. on day 1 of each 21-day cycle, followed by thoracic irradiation (total dose 60-65 Gy, daily fractions 1.8-2 Gy) with two concurrent courses of carboplatin/paclitaxel. 16.2% of the patients achieved complete response, 48.4% partial response, 25.8% stable disease and 9.6% progression of disease. Median progression-free and overall survival was 12 and 18 months, respectively. The most frequent haematological toxicities were grade (G) 3 anaemia in 19.3%, G3 neutropenia in 9.6% and G4 neutropenia in 12.9%. Esophageal G2 toxicity (RTOG) was observed in 28.1% of cases. The induction CT followed by concomitant chemoradiation used in this study appears feasible, safe and effective when administered to an unselected inoperable NSCLC stage III patient cohort in the everyday routine clinical practice. Further, our results are comparable to previously published phase III studies. (c) 2008 Elsevier Ireland Ltd. All rights reseved.
引用
收藏
页码:63 / 67
页数:5
相关论文
共 35 条
[1]
ALBERTI W, 1995, BRIT MED J, V311, P899
[2]
Concomitant radio-chemotherapy based on platin compounds in patients with locally advanced non-small cell lung cancer (NSCLC):: A meta-analysis of individual data from 1764 patients [J].
Aupérin, A ;
Le Péchoux, C ;
Pignon, JP ;
Koning, C ;
Jeremic, B ;
Clamon, G ;
Einhorn, L ;
Ball, D ;
Trovo, MG ;
Groen, HJM ;
Bonner, JA ;
Le Chevalier, T ;
Arriagada, R .
ANNALS OF ONCOLOGY, 2006, 17 (03) :473-483
[3]
Phase III study of the eastern cooperative oncology group (ECOG 2597): Induction chemotherapy followed by either standard thoracic radiotherapy or hyperfractionated accelerated radiotherapy for patients with unresectable stage IIIA and B non-small-cell lung cancer [J].
Belani, CP ;
Wang, W ;
Johnson, DH ;
Wagner, H ;
Schiller, J ;
Veeder, M ;
Mehta, M .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (16) :3760-3767
[4]
Combined chemoradiotherapy regimens of paclitaxel and carboplatin for locally advanced non-small-cell lung cancer: A randomized phase II locally advanced multi-modality protocol [J].
Belani, CP ;
Choy, H ;
Bonomi, P ;
Scott, C ;
Travis, P ;
Haluschak, J ;
Curran, WJ .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (25) :5883-5891
[5]
Randomised trial of sequential versus concurrent chemo-radiotherapy in patients with inoperable non-small cell lung cancer (EORTC 08972-22973) [J].
Belderbos, Jose ;
Uitterhoeve, Lon ;
van Zandwijk, Nico ;
Belderbos, Huub ;
Rodrigus, Patrick ;
van de Vaart, Paul ;
Belderbos, Huub ;
Rodrigus, Patrick ;
van de Vaart, Paul ;
Price, Allan ;
van Walree, Nico ;
Legrand, Catherine ;
Dussenneh, Sonia ;
Bartelink, Harry ;
Giaccone, Giuseppe ;
Koning, Caro .
EUROPEAN JOURNAL OF CANCER, 2007, 43 (01) :114-121
[6]
A RANDOMIZED PHASE-I/II TRIAL OF HYPERFRACTIONATED RADIATION-THERAPY WITH TOTAL DOSES OF 60.0 GY TO 79.2 GY - POSSIBLE SURVIVAL BENEFIT WITH GREATER-THAN-OR-EQUAL-TO 69.6 GY IN FAVORABLE PATIENTS WITH RADIATION-THERAPY ONCOLOGY GROUP STAGE-III NON-SMALL-CELL LUNG-CARCINOMA - REPORT OF RADIATION-THERAPY ONCOLOGY GROUP 83-11 [J].
COX, JD ;
AZARNIA, N ;
BYHARDT, RW ;
SHIN, KH ;
EMAMI, B ;
PAJAK, TF .
JOURNAL OF CLINICAL ONCOLOGY, 1990, 8 (09) :1543-1555
[7]
CURRAN W, 2000, P AM SOC CLIN ONCOL, V19
[8]
Improved survival in stage III non-small-cell lung cancer: Seven-year follow-up of cancer and leukemia group B (CALGB) 8433 trial [J].
Dillman, RO ;
Herndon, J ;
Seagren, SL ;
Eaton, WL ;
Green, MR .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1996, 88 (17) :1210-1215
[9]
An overview of eastern cooperative oncology group stage III non-small cell lung cancer studies [J].
Ettinger, DS .
SEMINARS IN ONCOLOGY, 2005, 32 (02) :S109-S110
[10]
Randomized phase III trial of sequential chemoradiotherapy compared with concurrent chemoradiotherapy in locally advanced non-small-cell lung cancer:: Groupe Lyon-Saint-Etienne d'Oncologie Thoracique-Groupe Francais de Pneumo-Cancerologie NPC 95-01 Study [J].
Fournel, P ;
Robinet, G ;
Thomas, P ;
Souquet, PJ ;
Léna, H ;
Vergnenégre, A ;
Delhoume, JY ;
Le Treut, J ;
Silvani, JA ;
Dansin, E ;
Bozonnat, MC ;
Daurés, JP ;
Mornex, F ;
Pérol, M .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (25) :5910-5917