A RANDOMIZED TRIAL OF 3 OR 6 COURSES OF ETOPOSIDE CYCLOPHOSPHAMIDE METHOTREXATE AND VINCRISTINE OR 6 COURSES OF ETOPOSIDE AND IFOSFAMIDE IN SMALL-CELL LUNG-CANCER (SCLC) .1. SURVIVAL AND PROGNOSTIC FACTORS

被引:38
作者
BLEEHEN, NM [1 ]
GIRLING, DJ [1 ]
MACHIN, D [1 ]
STEPHENS, RJ [1 ]
BARLEY, VL [1 ]
BULLIMORE, JA [1 ]
WHITE, RJ [1 ]
BLEEHAN, NM [1 ]
WILLIAMS, MV [1 ]
BREDIN, CP [1 ]
DAVIDSON, AR [1 ]
WILLIAMS, TJ [1 ]
ASH, DV [1 ]
CLOSE, HJ [1 ]
JOSLIN, CA [1 ]
MUERS, MF [1 ]
STONE, J [1 ]
ASHFORD, RF [1 ]
DISCHE, S [1 ]
DUNPHY, EP [1 ]
FERMONT, DC [1 ]
GROSCH, E [1 ]
MAHER, EJ [1 ]
SAUNDERS, MI [1 ]
ADAM, RJ [1 ]
ALCOCK, CJ [1 ]
BENSON, MK [1 ]
HOPKIN, JM [1 ]
LANE, DJ [1 ]
HUNTER, AM [1 ]
机构
[1] MRC,CANC TRIALS OFF,5 SHAFTESBURY RD,CAMBRIDGE CB2 2BW,ENGLAND
关键词
D O I
10.1038/bjc.1993.496
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
A total of 458 eligible patients, from 21 centres, with histologically or cytologically confirmed SCLC were allocated at random to three chemotherapy regimens, each given at 3-week intervals. In two regimens, etoposide, cyclophosphamide, methotrexate and vincristine were given for a total of either three courses (ECMV3) or six courses (ECMV6). In the third regimen, etoposide and ifosfamide were given for six courses (EI6). Patients with limited disease (56% of the total) also received radiotherapy to the primary site after the third course of chemotherapy in all three groups. A partial response occurred in 45% of 144 ECMV3 patients, 48% of 141 ECMV6, and 53% of 141 E16 patients assessed, and a complete response in a further 15%, 9%, and 13% respectively, giving total response rates of 60%, 57%, and 67%, respectively. There was no overall survival advantage to any of the three regimens. At 1 year, 24%, 29%, and 30% of patients were alive, and at 2 years 7%, 8%, and 9%, respectively. The median survival time was 7.4 months in the ECMV3 group, 8.6 months in the ECMV6 group and 8.8 months in the E16 group. The individual factors: poor performance status, extensive disease, the presence of dysphagia and a raised white blood cell count on admission adversely affected prognosis. The results do not exclude the possibility of a minor survival advantage with the two 6-course regimens. The findings on quality of life are presented in the companion paper (MRC Lung Cancer Working Party, 1993b).
引用
收藏
页码:1150 / 1156
页数:7
相关论文
共 18 条
[1]  
Altman, 1991, PRACTICAL STATICTS M
[2]   MAINTENANCE CHEMOTHERAPY FOR ANAPLASTIC SMALL CELL-CARCINOMA OF THE BRONCHUS - A RANDOMIZED, CONTROLLED TRIAL [J].
CULLEN, M ;
MORGAN, D ;
GREGORY, W ;
ROBINSON, M ;
COX, D ;
MCGIVERN, D ;
WARD, M ;
RICHARDS, M ;
STABLEFORTH, D ;
MACFARLANE, A ;
STIRLAND, J ;
WOODROFFE, C ;
MACFARLANE, J ;
FLETCHER, J ;
DAVIES, D .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 1986, 17 (02) :157-160
[3]   MAINTENANCE CHEMOTHERAPY IN SMALL-CELL LUNG-CANCER - LONG-TERM RESULTS OF A RANDOMIZED TRIAL [J].
GIACCONE, G ;
DALESIO, O ;
MCVIE, GJ ;
KIRKPATRICK, A ;
POSTMUS, PE ;
BURGHOUTS, JTM ;
BAKKER, W ;
KOOLEN, MGJ ;
VENDRIK, CPJ ;
ROOZENDAAL, KJ ;
PLANTING, AST ;
VANZANDWIJK, N ;
TENVELDE, GJM ;
SPLINTER, TAW .
JOURNAL OF CLINICAL ONCOLOGY, 1993, 11 (07) :1230-1240
[4]   MANAGEMENT OF SMALL-CELL CANCER OF THE LUNG [J].
HANSEN, HH .
LANCET, 1992, 339 (8797) :846-849
[5]  
HARPER PG, 1987, 4TH P EUR C CLIN ONC, V4, P2
[6]  
MACHIN D, 1989, BRIT MED J, P64
[7]   PATIENTS AT RISK OF CHEMOTHERAPY-ASSOCIATED TOXICITY IN SMALL CELL LUNG-CANCER [J].
MORITTU, L ;
EARL, HM ;
SOUHAMI, RL ;
ASH, CM ;
TOBIAS, JS ;
GEDDES, DM ;
HARPER, PG ;
SPIRO, SG .
BRITISH JOURNAL OF CANCER, 1989, 59 (05) :801-804
[8]   AN OVERVIEW OF PROGNOSTIC FACTORS IN SMALL-CELL LUNG-CANCER - A REPORT FROM THE SUBCOMMITTEE FOR THE MANAGEMENT OF LUNG-CANCER OF THE UNITED-KINGDOM COORDINATING COMMITTEE ON CANCER-RESEARCH [J].
RAWSON, NSB ;
PETO, J .
BRITISH JOURNAL OF CANCER, 1990, 61 (04) :597-604
[9]   DURATION OF CHEMOTHERAPY IN SMALL CELL LUNG-CANCER [J].
SPIRO, SG ;
SOUHAMI, RL .
THORAX, 1990, 45 (01) :1-2
[10]   DURATION OF CHEMOTHERAPY IN SMALL CELL LUNG-CANCER - A CANCER-RESEARCH CAMPAIGN TRIAL [J].
SPIRO, SG ;
SOUHAMI, RL ;
GEDDES, DM ;
ASH, CM ;
QUINN, H ;
HARPER, PG ;
TOBIAS, JS ;
PARTRIDGE, M ;
ERAUT, D .
BRITISH JOURNAL OF CANCER, 1989, 59 (04) :578-583