Cisplatin, mitomycin, and vindesine followed by intraoperative and postoperative radiotherapy for stage III non-small cell lung cancer: Final results of a phase II study

被引:6
作者
Aristu, J
Rebollo, J
MartinezMonge, R
Aramendia, JM
Viera, JC
Azinovic, I
Herreros, J
Brugarolas, A
机构
[1] UNIV NAVARRA CLIN, DEPT RADIAT ONCOL, PAMPLONA 31008, SPAIN
[2] UNIV NAVARRA CLIN, DEPT MED ONCOL, PAMPLONA 31008, SPAIN
[3] UNIV NAVARRA CLIN, DEPT CARDIOVASC & THORAC SURG, PAMPLONA 31008, SPAIN
来源
AMERICAN JOURNAL OF CLINICAL ONCOLOGY-CANCER CLINICAL TRIALS | 1997年 / 20卷 / 03期
关键词
non-small cell lung cancer; neoadjuvant chemotherapy; resectability; complete pathologic response; survival;
D O I
10.1097/00000421-199706000-00014
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Sixty-two patients with stage III non-small cell lung cancer (NSCLC) were treated with neoadjuvant chemotherapy consisting of cisplatin 120 mg/m(2) day 1, mitomycin 8 mg/m(2) day 1, and vindesine 3 mg/m(2) days 1 and 14. Each cycle was repeated every 4 weeks for a total of 1 to 6 cycles (median, 3 cycles). Resection was attempted 4 to 5 weeks after the last course of chemotherapy. Intraoperative radiation therapy (IORT) (10-15 Gy) was delivered during surgery and postoperative external beam radiotherapy (EBRT) (46 Gy) was begun 4 weeks after surgery. Fifty-five patients (25 IIIA, 30 IIIB) were evaluable. Only partial responses occurred (64%), and 29 patients (53%) underwent resection. Complete resection rates were 85% (12/14) and 40% (6/15) in stage IIIA and IIIB, respectively (p = 0.01). In 3 of 29 patients (10%), no tumor was found in the resected specimen. There was one chemotherapy-related death and three postoperative-related deaths. The median survival time was 10 months, and the 5-year survival rate was 29 and 7% for stage IIIA and stage IIIB, respectively (p = 0.3). High complete resection rates and modest increase in 5-year survival have been observed in stage IIIA NSCLC. Although a number of stage IIIB patients can be made technically resectable, the low complete resectability rate reflects the lack of survival benefit in these patients.
引用
收藏
页码:276 / 281
页数:6
相关论文
共 32 条
[1]
BITRAN JD, 1986, CANCER, V57, P44, DOI 10.1002/1097-0142(19860101)57:1<44::AID-CNCR2820570111>3.0.CO
[2]
2-H
[3]
INDUCTION CHEMOTHERAPY WITH MITOMYCIN, VINDESINE, AND CISPLATIN FOR STAGE-III UNRESECTABLE NON-SMALL-CELL LUNG-CANCER - RESULTS OF THE TORONTO PHASE-II TRIAL [J].
BURKES, RL ;
GINSBERG, RJ ;
SHEPHERD, FA ;
BLACKSTEIN, ME ;
GOLDBERG, ME ;
WATERS, PF ;
PATTERSON, GA ;
TODD, T ;
PEARSON, FG ;
COOPER, JD ;
JONES, D ;
LOCKWOOD, G .
JOURNAL OF CLINICAL ONCOLOGY, 1992, 10 (04) :580-586
[4]
A PHASE-I/II STUDY TO EVALUATE ACCELERATED FRACTIONATION VIA CONCOMITANT BOOST FOR SQUAMOUS, ADENO, AND LARGE-CELL CARCINOMA OF THE LUNG - REPORT OF RADIATION-THERAPY ONCOLOGY GROUP 84-07 [J].
BYHARDT, RW ;
PAJAK, TF ;
EMAMI, B ;
HERSKOVIC, A ;
DOGGETT, RS ;
OLSEN, LA .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1993, 26 (03) :459-468
[5]
INTRAOPERATIVE RADIOTHERAPY DURING LUNG-CANCER SURGERY - TECHNICAL DESCRIPTION AND EARLY CLINICAL-RESULTS [J].
CALVO, FA ;
DEURBINA, DO ;
ABUCHAIBE, O ;
AZINOVIC, I ;
ARISTU, J ;
SANTOS, M ;
ESCUDE, L ;
HERREROS, J ;
LLORENS, R .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1990, 19 (01) :103-109
[6]
CALVO FA, 1992, INTRAOPERATIVE RADIO, P43
[7]
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
[8]
A RANDOMIZED TRIAL OF INDUCTION CHEMOTHERAPY PLUS HIGH-DOSE RADIATION VERSUS RADIATION ALONE IN STAGE-III NON-SMALL-CELL LUNG-CANCER [J].
DILLMAN, RO ;
SEAGREN, SL ;
PROPERT, KJ ;
GUERRA, J ;
EATON, WL ;
PERRY, MC ;
CAREY, RW ;
FREI, EF ;
GREEN, MR .
NEW ENGLAND JOURNAL OF MEDICINE, 1990, 323 (14) :940-945
[9]
DONNADIEU N, 1991, LUNG CANCER, V7, P243
[10]
EAGAN RT, 1987, CANCER TREAT REP, V71, P895