Irinotecan (CPT-11) in combination with infusional 5-fluorouracil and leucovorin (de Gramont regimen) as first-line treatment in patients with advanced colorectal cancer - A multicenter phase II study

被引:19
作者
Vamvakas, L
Kakolyris, S
Kouroussis, C
Kandilis, K
Mavroudis, D
Ziras, N
Androulakis, N
Kalbakis, K
Sarra, E
Souglakos, J
Georgoulias, V
机构
[1] Univ Gen Hosp Heraklion, Dept Med Oncol, Iraklion 71110, Crete, Greece
[2] Agios Savas Anticanc Hosp Athens, Dept Med Oncol, Athens, Greece
[3] Agii Anargyri Anticanc Hosp Athens, Dept Med Oncol, Athens, Greece
来源
AMERICAN JOURNAL OF CLINICAL ONCOLOGY-CANCER CLINICAL TRIALS | 2002年 / 25卷 / 01期
关键词
5-FU; CPT-11; advanced colorectal cancer;
D O I
10.1097/00000421-200202000-00014
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The combination of CPT-11 with 5-fluorouracil (5-FU) in advanced colorectal cancer (ACC) represents an attractive approach. A phase 11 study was conducted to assess the tolerance and efficacy of CPT-11 in combination with leucovorin-modulated bolus plus infusional 5-FU given according to the de Gramont regimen in chemonaive patients with ACC. Fifty-four patients with histologically confirmed ACC were enrolled. The patients' median age was 65 years; 30 (55.5%) patients were men; performance status (World Health Organization) was 0 in 27 (50%) patients, 1 in 22 (41%), and 2 in 5 (9%). Patients received leucovorin (200 mg/m(2)/d) as a 2-hour intravenous infusion, followed by 5-FU as an intravenous bolus at 400 mg/m(2)/d, and then as a 22-hour continuous infusion at 600 mg/m(2)/d, repeated on 2 consecutive days. CPT-11 (180 mg/m(2); 30-minute intravenous infusion) was administered on day 1, simultaneously with leucovorin administration. This cycle was repeated every 2 weeks. Complete response was achieved in 4 patients (8%) and partial response in 19 (37%) (overall response rate: 45%; 95% CI: 24-50.5%). Stable disease was achieved in 16 (31%) patients and progressive disease in 13 (25%). The median duration of response and the median TTP were 5 and 8 months, respectively. After a median follow-up period of 11 months, 33 (61%) patients are still alive; the median overall survival has not yet been reached. Thrombocytopenia and anemia were very rare. Grade III/IV neutropenia developed in 19 patients (36%); febrile neutropenia developed in 4 patients, and 1 of them died of sepsis. Grade IV diarrhea was seen in 7 (13%) patients, and 4 of them required hospitalization. Grade III and IV mucositis was observed in two (4%) and one (2%) patients, respectively. Other toxicities were mild. The combination of CPT-11 and bolus plus infusional 5-FU is a relatively well-tolerated and effective first-line treatment in ACC. Final results from large phase III trials are awaited to clarify whether the CPT-11/5-FU combinations should be considered as "standard" first-line treatment in ACC.
引用
收藏
页码:65 / 70
页数:6
相关论文
共 33 条
[1]  
[Anonymous], 1989, Analysis of binary data
[2]   Randomized trial comparing monthly low-dose leucovorin and fluorouracil bolus with weekly high-dose 48-hour continuous-infusion fluorouracil for advanced colorectal cancer: A Spanish Cooperative Group for Gastrointestinal Tumor Therapy (TTD) study [J].
Aranda, E ;
Diaz-Rubio, E ;
Cervantes, A ;
Anton-Torres, A ;
Carrato, A ;
Massuti, T ;
Tabernero, JM ;
Sastre, J ;
Tres, A ;
Aparicio, J ;
Lopez-Vega, JM ;
Barneto, I ;
Garcia-Conde, T .
ANNALS OF ONCOLOGY, 1998, 9 (07) :727-731
[3]   CPT-II (IRINOTECAN) IN THE TREATMENT OF COLORECTAL-CANCER [J].
ARMAND, JP ;
DUCREUX, M ;
MAHJOUBI, M ;
ABIGERGES, D ;
BUGAT, R ;
CHABOT, G ;
HERAIT, P ;
DEFORNI, M ;
ROUGIER, P .
EUROPEAN JOURNAL OF CANCER, 1995, 31A (7-8) :1283-1287
[4]  
BLEIBERG H, 1996, EUR J CANCER, V32, P18
[5]   RANDOMIZED COMPARISON OF 2 SCHEDULES OF FLUOROURACIL AND LEUCOVORIN IN THE TREATMENT OF ADVANCED COLORECTAL-CANCER [J].
BUROKER, TR ;
OCONNELL, MJ ;
WIEAND, HS ;
KROOK, JE ;
GERSTNER, JB ;
MAILLIARD, JA ;
SCHAEFER, PL ;
LEVITT, R ;
KARDINAL, CG ;
GESME, DH .
JOURNAL OF CLINICAL ONCOLOGY, 1994, 12 (01) :14-20
[6]  
COMELLA P, 1999, P AM SOC CLIN ONCOL, V18, P281
[7]   Irinotecan is an active agent in untreated patients with metastatic colorectal cancer [J].
Conti, JA ;
Kemeny, NE ;
Saltz, LB ;
Huang, Y ;
Tong, WP ;
Chou, TC ;
Sun, M ;
Pulliam, S ;
Gonzalez, C .
JOURNAL OF CLINICAL ONCOLOGY, 1996, 14 (03) :709-715
[8]   Randomised trial of irinotecan plus supportive care versus supportive care alone after fluorouracil failure for patients with metastatic colorectal cancer [J].
Cunningham, D ;
Pyrhönen, S ;
James, RD ;
Punt, CJA ;
Hickish, TF ;
Heikkila, R ;
Johannesen, TB ;
Starkhammar, H ;
Topham, CA ;
Awad, L ;
Jacques, C ;
Herait, P .
LANCET, 1998, 352 (9138) :1413-1418
[9]   HIGH-DOSE FOLINIC ACID AND 5-FLUOROURACIL BOLUS AND CONTINUOUS INFUSION IN ADVANCED COLORECTAL-CANCER [J].
DEGRAMONT, A ;
KRULIK, M ;
CADY, J ;
LAGADEC, B ;
MAISANI, JE ;
LOISEAU, JP ;
GRANGE, JD ;
GONZALEZCANALL, G ;
DEMUYNCK, B ;
LOUVET, C ;
SEROKA, J ;
DRAY, C ;
DEBRAY, J .
EUROPEAN JOURNAL OF CANCER & CLINICAL ONCOLOGY, 1988, 24 (09) :1499-1503
[10]   Randomized trial comparing monthly low-dose leucovorin and fluorouracil bolus with bimonthly high-dose leucovorin and fluorouracil bolus plus continuous infusion for advanced colorectal cancer: A French intergroup study [J].
deGramont, A ;
Basset, JF ;
Milan, C ;
Rougier, P ;
Bouche, O ;
Etienne, PL ;
Morvan, F ;
Louvet, C ;
Guillot, C ;
Francois, E ;
Bedenne, L .
JOURNAL OF CLINICAL ONCOLOGY, 1997, 15 (02) :808-815