Department of Epidemiology, Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.
Department of Hematology/Oncology, LMU Klinikum, University of Munich, Comprehensive Cancer Center Munich, Munich, Germany.
ESMO Open. 2023 Apr;8(2):101199. doi: 10.1016/j.esmoop.2023.101199. Epub 2023 Apr 3.
Fluoropyrimidines (FPs) are an essential part of the majority of systemic regimens in the treatment of metastatic colorectal cancer (CRC). The use of the oral FP S-1 has been approved by the European Medicines Agency as monotherapy or in combination with oxaliplatin or irinotecan, with or without bevacizumab, for the treatment of patients with metastatic CRC in whom it is not possible to continue treatment with another FP due to hand-foot syndrome (HFS) or cardiovascular toxicity (CVT). Subsequently, this indication has been included in the 2022 ESMO guidelines for metastatic CRC. Recommendations for use in daily practice are not available.
Based on peer-reviewed published data on the use of S-1 in Western patients with metastatic CRC who switched from infusional 5-fluorouracil (5-FU) or capecitabine to S-1 for reasons of HFS or CVT, recommendations for its use were formulated by an international group of medical oncologists with expertise in the treatment of metastatic CRC and a cardio-oncologist.
In patients who experience pain and/or functional impairment due to HFS during treatment with capecitabine or infusional 5-FU, a switch to S-1 is recommended without prior dose reduction of capecitabine/5-FU. S-1 should preferably be initiated at full dose when HFS has decreased to grade ≤1. In patients with cardiac complaints, in whom an association with capecitabine or infusional 5-FU treatment cannot be excluded, capecitabine/5-FU should be discontinued and a switch to S-1 is recommended.
These recommendations should guide clinicians in daily practice in the treatment of patients with metastatic CRC with FP-containing regimens.
氟嘧啶类药物(FPs)是治疗转移性结直肠癌(CRC)的大多数系统治疗方案的重要组成部分。欧洲药品管理局已批准口服 FP S-1 单药治疗或联合奥沙利铂或伊立替康,联合或不联合贝伐珠单抗,用于因手足综合征(HFS)或心血管毒性(CVT)而无法继续使用另一种 FP 治疗的转移性 CRC 患者。随后,这一适应证被纳入 2022 年 ESMO 转移性 CRC 指南。目前尚无关于其在日常实践中应用的推荐意见。
根据在西方转移性 CRC 患者中使用 S-1 的同行评议已发表数据,这些患者因 HFS 或 CVT 而从输注 5-氟尿嘧啶(5-FU)或卡培他滨转换为 S-1,由具有转移性 CRC 治疗专业知识的国际肿瘤学家小组和一名心脏肿瘤学家制定了 S-1 的使用建议。
在接受卡培他滨或输注 5-FU 治疗时因 HFS 出现疼痛和/或功能障碍的患者中,建议在不减少卡培他滨/5-FU 剂量的情况下转换为 S-1。当 HFS 降至≤1 级时,建议首选 S-1 全剂量起始。对于有心脏不适的患者,不能排除与卡培他滨或输注 5-FU 治疗相关的情况,应停止卡培他滨/5-FU 治疗并建议转换为 S-1。
这些建议应指导临床医生在含有 FP 的方案治疗转移性 CRC 患者的日常实践中进行治疗。