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.
引用
收藏
页码:2745 / 2751
页数:7
相关论文
共 50 条
  • [41] Phase II trial of panitumumab with irinotecan as salvage therapy for patients with advanced or recurrent colorectal cancer (TOPIC study)
    Nishi, Tomohiro
    Hamamoto, Yasuo
    Nagase, Michitaka
    Denda, Tadamichi
    Yamaguchi, Kensei
    Amagai, Kenji
    Miyata, Yoshinori
    Yamanaka, Yasuhiro
    Yanai, Kai
    Ishikawa, Tsutomu
    Kuroki, Yoshifumi
    Fujii, Hirofumi
    ONCOLOGY LETTERS, 2016, 11 (06) : 4049 - 4054
  • [42] A phase II study of combination therapy with irinotecan and S-1 (IRIS) in patients with advanced colorectal cancer
    Shiozawa, Manabu
    Akaike, Makoto
    Sugano, Nobuhiro
    Tsuchida, Kazuhito
    Yamamoto, Naoto
    Morinaga, Soichiro
    CANCER CHEMOTHERAPY AND PHARMACOLOGY, 2010, 66 (05) : 987 - 992
  • [43] Angiogenesis modifications are predictive of response and outcome advanced colorectal cancer patients during therapy with cetuximab plus irinotecan
    Vincenzi, Bruno
    Santini, Daniele
    Russo, Antonio
    Dicuonzo, Giordano
    Gavasci, Michele
    Battistoni, Fabrizio
    Rocci, Laura
    Gebbia, Nicola
    Tonini, Giuseppe
    ANNALS OF ONCOLOGY, 2006, 17 : 258 - 258
  • [44] Phase II, prospective, open-label study of a weekly schedule of irinotecan in patients with advanced colorectal cancer.
    Casinello, J
    Dorta, J
    Aguiar, J
    Pérez-Carrión, J
    Castellanos, J
    Valladares, J
    Sevilla, J
    Belón, J
    Fernández, J
    Casal, J
    ANNALS OF ONCOLOGY, 2000, 11 : 46 - 46
  • [45] Irinotecan (CPT-11) in advanced colorectal cancer patients with progression after therapy with 5-FU.
    Mendez, M
    Salud, A
    García, C
    Navalón, M
    España, P
    Cruz, JJ
    Diz, P
    del Val, G
    del Prado, M
    ANNALS OF ONCOLOGY, 2000, 11 : 56 - 56
  • [46] Angiogenesis modifications are predictive of response and outcome advanced colorectal cancer patients during therapy with cetuximab plus irinotecan
    Vincenzi, B.
    Santini, D.
    Russo, A.
    Dicuonzo, G.
    Michele, G.
    Battistoni, F.
    Rocci, L.
    Gebbia, N.
    Tonini, G.
    ANNALS OF ONCOLOGY, 2006, 17 : XI39 - XI39
  • [47] Phase I study of TAS-102 and irinotecan combination therapy in Japanese patients with advanced colorectal cancer
    Toshihiko Doi
    Takayuki Yoshino
    Nozomu Fuse
    Narikazu Boku
    Kentaro Yamazaki
    Wasaburo Koizumi
    Ken Shimada
    Yasutaka Takinishi
    Atsushi Ohtsu
    Investigational New Drugs, 2015, 33 : 1068 - 1077
  • [48] Prospective, double-blind, placebo-controlled, multicenter, randomized phase III study with orally administered budesonide for prevention of irinotecan (CPT-11)-induced diarrhea in patients with advanced colorectal cancer
    Karthaus, M
    Ballo, H
    Abenhardt, W
    Steinmetz, T
    Geer, T
    Schimke, J
    Braumann, D
    Behrens, R
    Behringer, D
    Kindler, M
    Messmann, H
    Boeck, HP
    Greinwald, R
    Kleeberg, U
    ONCOLOGY, 2005, 68 (4-6) : 326 - 332
  • [49] Phase I study of TAS-102 and irinotecan combination therapy in Japanese patients with advanced colorectal cancer
    Doi, Toshihiko
    Yoshino, Takayuki
    Fuse, Nozomu
    Boku, Narikazu
    Yamazaki, Kentaro
    Koizumi, Wasaburo
    Shimada, Ken
    Takinishi, Yasutaka
    Ohtsu, Atsushi
    INVESTIGATIONAL NEW DRUGS, 2015, 33 (05) : 1068 - 1077
  • [50] Biweekly cetuximab and irinotecan as third-line therapy in patients with advanced colorectal cancer after failure to irinotecan, oxaliplatin and 5-fluorouracil
    Pfeiffer, P.
    Nielsen, D.
    Bjerregaard, J.
    Qvortrup, C.
    Yilmaz, M.
    Jensen, B.
    ANNALS OF ONCOLOGY, 2008, 19 (06) : 1141 - 1145