荷兰同步和异时性转移性结直肠癌患者的现实世界治疗模式和生存率

M.A.G. Elferink , F.N. van Erning , F.C. Sijtsma , L.B. Valkenburg-van Iersel , M.L. Wumkes , J.M.L. Roodhart , G.R. Vink
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引用次数: 0

摘要

背景:在转移性结直肠癌(mCRC)患者的日常治疗实践中,对现实世界治疗模式的了解是有限的。这项基于人群的研究的目的是提供mCRC患者的治疗和总生存期(OS)的概述,并比较同步和非同步mCRC治疗的差异。方法选择2015年上半年诊断为原发肿瘤的所有mCRC患者,这些患者来自荷兰癌症登记处。2019年收集了后续治疗的数据。比较同步和异时mCRC患者的治疗模式。采用Kaplan-Meier法分析OS。结果共纳入同步型mCRC患者1532例,异时型mCRC患者870例。异时性mCRC患者更常接受远处转移的局部治疗(P <;0.001)。大约一半的患者在诊断为mCRC后接受了全身治疗(ST),同步型和异时型mCRC的ST类型差异很小。奥沙利铂和伊立替康分别是主要的一线和二线全身治疗方案。所有mCRC患者的中位OS为16.0个月[95%置信区间(CI) 15.0-17.0个月]。从每条后续治疗线开始的中位OS中,开始一线ST的患者为16.3个月(95% CI 15.5-17.5个月),开始二线ST的患者为8.9个月(95% CI 8.3-9.7个月),开始三线ST的患者为6.1个月(95% CI 5.4-6.7个月)。结论真实世界的数据为mCRC患者在日常临床实践中提供了宝贵的见解,使临床医生能够为患者提供更明智的指导。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Real-world treatment patterns and survival in patients with synchronous and metachronous metastatic colorectal cancer in the Netherlands

Background

Insight into real-world treatment patterns in daily practice of patients with metastatic colorectal cancer (mCRC) is limited. Aim of this population-based study is to provide an overview of treatment and overall survival (OS) of patients with mCRC and to compare differences in treatment between synchronous and metachronous mCRC.

Method

All patients with mCRC of whom the primary tumour was diagnosed in the first half of 2015 were selected from the Netherlands Cancer Registry. Data regarding subsequent treatments were collected in 2019. Treatment patterns were compared between patients with synchronous and metachronous mCRC. OS was analysed using the Kaplan–Meier method.

Results

In total, 1532 patients with synchronous mCRC and 870 patients with metachronous mCRC were included. Patients with metachronous mCRC more often underwent local treatment of distant metastases (P < 0.001). Approximately half of the patients received systemic treatment (ST) after diagnosis of mCRC, with small differences in type of ST between synchronous and metachronous mCRC. Oxaliplatin- and irinotecan-containing regimens were the predominant first- and second-line systemic therapies, respectively. Median OS of all patients with mCRC was 16.0 months [95% confidence interval (CI) 15.0-17.0 months]. Median OS from the start of each subsequent treatment line was 16.3 months (95% CI 15.5-17.5 months) for patients who started first-line ST, 8.9 months (95% CI 8.3-9.7 months) for patients who started second-line ST and 6.1 months (95% CI 5.4-6.7 months) for patients who started third-line ST.

Conclusions

Real-world data offer valuable insights for mCRC patients in everyday clinical practice, enabling clinicians to provide more informed guidance to their patients.
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