Pathophysiology and therapy of irinotecan-induced delayed-onset diarrhea in patients with advanced colorectal cancer: A prospective assessment

被引:121
|
作者
Saliba, F
Hagipantelli, R
Misset, JL
Bastian, G
Vassal, G
Bonnay, M
Herait, P
Cote, C
Mahjoubi, M
Mignard, D
Cvitkovic, E
机构
[1] Hop Paul Brousse, FSMSIT, F-94804 Villejuif, France
[2] Inst Gustave Roussy, Villejuif, France
[3] Hop La Pitie Salpetriere, Paris, France
[4] Grp Rhone Poulenc Rorer, Montrouge, France
关键词
D O I
10.1200/JCO.1998.16.8.2745
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Irinotecan(CPT-I I),a camptothecin derivative, has shown efficacy against colorectal cancer. Delayed-onset diarrhea is its main limiting toxicity. The aim of this study was to determine the pathophysiology of CPT-ll-induced delayed-onset diarrhea and assess the efficacy of combined antidiarrheal medication in a phase II, prospective, successive-cohorts, open study. Patients and Methods: Twenty-eight patients with advanced colorectal cancer refractory to fluorouracil (5-FU) therapy received CPT-11 350 mg/m(2) every 3 weeks. The first cohort of 14 consecutive patients explored for the mechanism of diarrhea received acetorphan (a new enkephalinase inhibitor) 100 mg three rimes daily; the second 14-patient cohort received, in addition to acetorphan, loperamide 4 mg three times daily. Before treatment, and if late diarrhea occurred, patients underwent colon mucosal biopsies for CPT-II and tapoisomerase I levels; intestinal transit time; fecalogram; far and protein excretion; alpha(1)-antitrypsin clearance; D-xylose test; blood levels for vasoactive intestinal polypeptide, glucagon, gastrin, somatostatin, prostaglandin E-2 and carboxylesterase; CPT-11/SN-38 and SN-38 glucuronide pharmacokinetics; and stool cultures. Results: Delayed-onset diarrhea occurred during the first three treatment cycles in 23 patients (82%). Electrolyte fecal measurements showed a negative or small osmotic gap in nine of nine patients and an increased alpha(1)-antitrypsin clearance in six of six patients. There were no modifications in stool cultures or hormonal dysfunction. Four of 11 patients (36%) with delayed-onset diarrhea in the first cohort responded to acetorphan, whereas nine of 10 patients (90%) responded to the combination of acetorphan and loperamide (P <.02). Conclusion: CPT-11-induced delayed-onset diarrhea is caused by a secretory mechanism with an exudative component. Early combined treatment with loperamide and acetorphan seems effective in controlling the diarrheal episodes. J Clin Oncol 16:2745-2751. (C) 1998 by American Society of Clinical Oncology.
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页码:2745 / 2751
页数:7
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