COMBINATION CHEMOTHERAPY WITH TENIPOSIDE (VM26) AND CARBOPLATIN IN SMALL-CELL LUNG-CANCER

被引:4
作者
GOSS, GD
VINCENT, M
GERMOND, C
CORRINGHAM, S
ROWEN, J
DHALIWAL, H
CORRINGHAM, R
机构
[1] UNIV OTTAWA,NE ONTARIO REG CANC CTR,FAC HLTH SCI,OTTAWA K1N 6N5,ONTARIO,CANADA
[2] UNIV OTTAWA,FAC HLTH SCI,ONTARIO CANC TREATMENT & RES FDN,OTTAWA K1N 6N5,ONTARIO,CANADA
[3] MCMASTER UNIV,FAC HLTH SCI,THUNDER BAY REG CANC CTR,ONTARIO CANC TREATMENT & RES FDN,HAMILTON L8S 4L8,ONTARIO,CANADA
来源
AMERICAN JOURNAL OF CLINICAL ONCOLOGY-CANCER CLINICAL TRIALS | 1993年 / 16卷 / 04期
关键词
SMALL CELL LUNG CANCER; TENIPOSIDE; CARBOPLATIN;
D O I
10.1097/00000421-199308000-00004
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Seventy patients with previously untreated histologically proven small cell lung cancer (SCLC) were treated with a combination of teniposide 60 mg/m2 intravenously (i.v.) on days 1 through 5 and carboplatin 400 mg/m2 i.v. on day 1 every 28 days for six courses. Patients with limited stage disease, (LD) who achieved a response, subsequently received 2,000 cGy prophylactic cranial and 3,000 cGy involved field thoracic radiotherapy. Of the 70 patients, 62 were evaluable for response: 47 patients (76%) achieved an objective response; 14 of 29 patients (48%) with LD had a complete response (CR), with a partial response (PR) plus CR rate of 76%. Seven of 33 patients (2 1 %) with extensive disease (ED) achieved a CR, with a combined PR and CR rate of 76%. Median time to progression (TTP) for all responders was 292 days (42 weeks). Median duration of survival for all LD patients was 415 days (59 weeks). Survival for LD patients was 88% at 6 months, 6 1 % at 12 months, and 29% at 18 months. Median survival duration for all patients in the study was 311 days (44 weeks), with a survival of 79% at 6 months, 44% at 1 year, and 16% at 18 months. Myelosuppression was the main toxicity, with World Health Organization (WHO) grade 3 or 4 infection occurring in 33% of patients. Two patients died of pneumonia, one complicated by renal failure, and another suffered cardiac arrest related to treatment. The high activity of this drug combination justifies its use as a first-line treatment of previously untreated SCLC.
引用
收藏
页码:295 / 300
页数:6
相关论文
共 21 条
[1]  
[Anonymous], 1979, WHO HDB REPORTING RE
[2]   TENIPOSIDE AND ETOPOSIDE IN PREVIOUSLY UNTREATED SMALL-CELL LUNG-CANCER - A RANDOMIZED STUDY [J].
BORK, E ;
ERSBOLL, J ;
DOMBERNOWSKY, P ;
BERGMAN, B ;
HANSEN, M ;
HANSEN, HH .
JOURNAL OF CLINICAL ONCOLOGY, 1991, 9 (09) :1627-1631
[3]   TENIPOSIDE (VM-26), AN OVERLOOKED HIGHLY-ACTIVE AGENT IN SMALL-CELL LUNG-CANCER - RESULTS OF A PHASE-II TRIAL IN UNTREATED PATIENTS [J].
BORK, E ;
HANSEN, M ;
DOMBERNOWSKY, P ;
HANSEN, SW ;
PEDERSEN, AG ;
HANSEN, HH .
JOURNAL OF CLINICAL ONCOLOGY, 1986, 4 (04) :524-527
[4]  
BORK E, 1989, P AM SOC CLIN ONCOL, V8, pA890
[5]   EARLY CLINICAL-STUDIES WITH CIS-DIAMMINE-1,1-CYCLOBUTANE DICARBOXYLATE PLATINUM-II [J].
CALVERT, AH ;
HARLAND, SJ ;
NEWELL, DR ;
SIDDIK, ZH ;
JONES, AC ;
MCELWAIN, TJ ;
RAJU, S ;
WILTSHAW, E ;
SMITH, IE ;
BAKER, JM ;
PECKHAM, MJ ;
HARRAP, KR .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 1982, 9 (03) :140-147
[6]  
CANNETTA R, 1988, CANCER TREAT REV SB, V15, P17
[7]  
EVANS WK, 1986, SEMIN ONCOL, V13, P17
[8]   HIGH-DOSE CARBOPLATIN IN THE TREATMENT OF LUNG-CANCER AND MESOTHELIOMA - A PHASE-I DOSE ESCALATION STUDY [J].
GORE, ME ;
CALVERT, AH ;
SMITH, IE .
EUROPEAN JOURNAL OF CANCER & CLINICAL ONCOLOGY, 1987, 23 (09) :1391-1397
[9]  
IHDE DC, 1981, SMALL CELL LUNG CANC, P261
[10]  
JACOBS RH, 1987, CANCER TREAT REP, V71, P311