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接受一线化疗的晚期和复发性结直肠癌患者的预后因素。

Prognostic factors in patients with advanced and recurrent colorectal cancer receiving last-line chemotherapy.

作者信息

Kimura M, Iwai M, Usami E, Teramachi H, Yoshimura T

出版信息

Pharmazie. 2018 Feb 1;73(2):115-119. doi: 10.1691/ph.2018.7832.

Abstract

For patients with advanced/recurrent colorectal cancer, the trifluridine/tipiracil combination tablet (TAS 102) and regorafenib are last-line treatments. This study aimed to clarify prognostic factors in patients receiving last-line chemotherapy. Between April 2014 and December 2016, 47 patients received last-line chemotherapy at Ogaki Municipal Hospital, Japan. The primary outcome was overall survival. To determine factors associated with survival, those considered significant in the univariate analysis (p <0.10), were entered into a multivariate Cox proportional hazards model. KRAS type and the use of opioid formulations were independently and significantly associated with survival in the multivariate analysis. For patients with KRAS-wild relative to KRAS-mutation cancers, the hazard ratio for death was 0.478 (95% CI, 0.249-0.919; p = 0.03). For patients taking opioid formulations, relative to those not, the hazard ratio for death was 3.557 (95% CI, 1.032-12.257; p = 0.04). The median overall survival duration for patients with KRAS-wild (n = 24) and KRAS-mutation (n = 23) cancers were 223.5 days (range: 115-703) and 154 days (range: 51-503), respectively (p = 0.05). This finding provides a useful index to make an early decision on discontinuation of treatment and to guide decisions around agents to use in last-line chemotherapy.

摘要

对于晚期/复发性结直肠癌患者,曲氟尿苷/替匹嘧啶复方片剂(TAS 102)和瑞戈非尼是一线治疗药物。本研究旨在明确接受一线化疗患者的预后因素。2014年4月至2016年12月期间,47例患者在日本大垣市立医院接受一线化疗。主要结局指标为总生存期。为确定与生存相关的因素,将单因素分析中具有显著意义(p<0.10)的因素纳入多因素Cox比例风险模型。多因素分析显示,KRAS类型和阿片类制剂的使用与生存独立且显著相关。KRAS野生型癌症患者相对于KRAS突变型癌症患者,死亡风险比为0.478(95%CI,0.249-0.919;p=0.03)。服用阿片类制剂的患者相对于未服用者,死亡风险比为3.557(95%CI,1.032-12.257;p=0.04)。KRAS野生型(n=24)和KRAS突变型(n=23)癌症患者的中位总生存期分别为223.5天(范围:115-703)和154天(范围:51-503)(p=0.05)。这一发现为早期决定停止治疗以及指导一线化疗药物的选择提供了有用的指标。

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