Alternative Treatment Options in Colorectal Cancer Patients With 5-Fluorouracil- or Capecitabine-Induced Cardiotoxicity

被引:48
作者
Deboever, Guido [1 ]
Hiltrop, Nick [2 ]
Cool, Mike [1 ]
Lambrecht, Guy [1 ]
机构
[1] AZ Damiaan Ziekenhuis, Dept Gastroenterol Hepatol Digest Oncol, B-8400 Oostende, Belgium
[2] Katholieke Univ Leuven, Univ ZiekenhuizenLeuven, Dept Cardiol, Louvain, Belgium
关键词
Chemotherapy; Fluoropyrimidine-induced toxicity; Raltitrexed; S-1; PHASE-III TRIAL; CETUXIMAB PLUS IRINOTECAN; 1ST-LINE TREATMENT; BOLUS; 5-FLUOROURACIL; RALTITREXED TOMUDEX; 2ND-LINE TREATMENT; RANDOMIZED-TRIAL; ORAL LEUCOVORIN; OXALIPLATIN; FLUOROURACIL;
D O I
10.1016/j.clcc.2012.09.003
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Most chemotherapy regimens in colorectal cancer treatment are 5-fluorouracil (5-FU)/leucovorin or capecitabine-based. Cardiotoxicity is a less common but potentially lethal complication of 5-FU or capecitabine treatment, and some physicians might be unfamiliar with treatment alternatives. Rechallenging should be avoided because it carries a high risk of recurrence of the cardiac symptoms and prophylactic treatment is not always protective. Possible alternative treatment options to be considered are to replace the oral capecitabine or intravenous 5-FU by a 5-FU bolus regimen, by uracil-tegafur or tegafur/gimeracil/oteracil, both oral fluoro-pyrimidines combining a 5-FU prodrug with a dihydropyrimidine dehydrogenase (DPD) inhibitor, or by raltitrexed, a thymidilate synthase inhibitor whose metabolism is independent of DPD. Patients with advanced colorectal cancer and fluoropyrimidine-induced cardiotoxicity can be treated with other non-fluoropyrinnidine related chemotherapy, either as a single agent, combined, or in combination with biological agents. In this report we discuss the different alternative treatment options. Clinical Colorectal Cancer, Vol. 12, No. 1, 8-14 (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:8 / 14
页数:7
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