Irinotecan (CPT-11) in patients with advanced colon carcinoma relapsing after 5-fluorouracil-leucovorin combination

被引:14
作者
Tsavaris, NB
Polyzos, A
Gennatas, K
Kosmas, C
Vadiaka, M
Dimitrakopoulos, A
Macheras, A
Papastratis, G
Tsipras, H
Margaris, H
Papalambros, E
Giannopoulos, A
Koufos, C
机构
[1] Univ Athens, Sch Med, Laikon Gen Hosp, Dept Pathophysiol,Oncol Unit, GR-11527 Athens, Greece
[2] Univ Athens, Sch Med, Laikon Gen Hosp, Dept Internal Med Propedeut 1,Oncol Unit, GR-11527 Athens, Greece
[3] Areteion Hosp, Oncol Unit, Athens, Greece
[4] Univ Athens, Sch Med, Sotiria Hosp, Surg Dept 3, GR-11527 Athens, Greece
[5] Genimatas Gen Hosp, Surg Dept 3, Athens, Greece
[6] Univ Athens, Sch Med, Laikon Gen Hosp, Dept Surg 1, GR-11527 Athens, Greece
关键词
CPT-11; advanced colon carcinoma; performance status; 5-fluorouracil; leucovorin;
D O I
10.1159/000057669
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The purpose of the present study was to investigate the association between performance status (PS) and mean dose of irinotecan (CPT-11) in patients with recurrent advanced colorectal cancer relapsing after 5-fluorouracil and leucovorin chemotherapy. Patients who had completed their last chemotherapy course with 5-fluorouracil and leucovorin for at least 6 weeks and progressed were included. Based on PS, we administered a starting dose of 250 mg/m(2) in patients with a PS 70-80 (group A), and 350 mg/m(2) for those with a PS > 80 (group B). Of a total of 90 treated patients, all were evaluable, 18 had a partial response (PR) (20%), 39 stable disease (43%), and 15 progressed (37%). No significant difference was noticed between patients with PS greater than or equal to90 or less than or equal to80 (p = 0.925), or between those who received a mean dose of CPT-11 greater than or equal to300 or less than or equal to300 (p = 0.602), for response, survival and time to progression. Toxicity was increased in group B as expected, with significant differences for acute cholinergic syndrome (p = 0.02), diarrhea after the first 24 h (p = 0.03) and severe diarrhea (p = 0.03). According to these results, we conclude that response to CPT-11 is independent of its dose, and that a dose of 250 mg/m(2) every 3 weeks might be a cost-effective and less toxic alternative in this setting. However, further adequately powered phase II or III randomized studies might be required in order to confirm this observation. Copyright (C) 2002 S. Karger AG, Basel.
引用
收藏
页码:94 / 99
页数:6
相关论文
共 12 条
[1]   PROGNOSTIC VALUE OF NEURAL INVASION IN RECTAL-CARCINOMA - A MULTIVARIATE-ANALYSIS ON 339 PATIENTS WITH CURATIVE RESECTION [J].
BOGNEL, C ;
REKACEWICZ, C ;
MANKARIOS, H ;
PIGNON, JP ;
ELIAS, D ;
DUVILLARD, P ;
PRADE, M ;
DUCREUX, M ;
KAC, J ;
ROUGIER, P ;
ESCHWEGE, F ;
LASSER, P .
EUROPEAN JOURNAL OF CANCER, 1995, 31A (06) :894-898
[2]  
CONTI JA, 1994, P AN M AM SOC CLIN, V13, P195
[3]   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
[4]   DNA TOPOISOMERASE-I TARGETED CHEMOTHERAPY OF HUMAN-COLON CANCER IN XENOGRAFTS [J].
GIOVANELLA, BC ;
STEHLIN, JS ;
WALL, ME ;
WANI, MC ;
NICHOLAS, AW ;
LIU, LF ;
SILBER, R ;
POTMESIL, M .
SCIENCE, 1989, 246 (4933) :1046-1048
[5]  
GUPTA E, 1994, CANCER RES, V54, P3723
[6]   NONPARAMETRIC-ESTIMATION FROM INCOMPLETE OBSERVATIONS [J].
KAPLAN, EL ;
MEIER, P .
JOURNAL OF THE AMERICAN STATISTICAL ASSOCIATION, 1958, 53 (282) :457-481
[7]  
MANTEL NATHAN, 1966, CANCERCHEMOTHERAP REP, V50, P163
[8]  
MILLER AB, 1981, CANCER, V47, P207, DOI 10.1002/1097-0142(19810101)47:1<207::AID-CNCR2820470134>3.0.CO
[9]  
2-6
[10]  
PITOT HC, 1994, P AM SOC CLIN ONCOL, V13, P197