Efficacy of chemotherapy containing bevacizumab in patients with metastatic colorectal cancer according to programmed cell death ligand 1.

IF 2.5 4区 医学 Q2 GASTROENTEROLOGY & HEPATOLOGY
Shin Woo Kang, Sung Hee Lim, Min-Ji Kim, Jeeyun Lee, Young Suk Park, Ho Yeong Lim, Won Ki Kang, Seung Tae Kim
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引用次数: 0

Abstract

Background: Bevacizumab, an anti-vascular endothelial growth factor (VEGF) monoclonal antibody, inhibits angiogenesis and reduces tumor growth. Serum VEGF-C, lactate dehydrogenase, and inflammatory markers have been reported as predictive markers related to bevacizumab treatment. Programmed cell death ligand 1 (PD-L1) could act upon VEGF receptor 2 to induce cancer cell angiogenesis and metastasis.

Aim: To investigate the efficacy of bevacizumab-containing chemotherapy in patients with metastatic colorectal cancer (CRC) according to the expression of PD-L1.

Methods: This analysis included CRC patients who received bevacizumab plus FOLFOX or FOLFIRI as first-line therapy between June 24, 2014 and February 28, 2022, at Samsung Medical Center (Seoul, South Korea). Analysis of patient data included evaluation of PD-L1 expression by the combined positive score (CPS). We analyzed the efficacy of bevacizumab according to PD-L1 expression status in patients with CRC.

Results: A total of 124 patients was included in this analysis. Almost all patients were treated with bevacizumab plus FOLFIRI or FOLFOX as the first-line chemotherapy. While 77% of patients received FOLFOX, 23% received FOLFIRI as backbone first-line chemotherapy. The numbers of patients with a PD-L1 CPS of 1 or more, 5 or more, or 10 or more were 105 (85%), 64 (52%), and 32 (26%), respectively. The results showed no significant difference in progression-free survival (PFS) and overall survival (OS) with bevacizumab treatment between patients with PD-L1 CPS less than 1 and those with PD-L1 CPS of 1 or more (PD-L1 < 1% vs PD-L1 ≥ 1%; PFS: P = 0.93, OS: P = 0.33), between patients with PD-L1 CPS less than 5 and of 5 or more (PD-L1 < 5% vs PD-L1 ≥ 5%; PFS: P = 0.409, OS: P = 0.746), and between patients with PD-L1 CPS less than 10 and of 10 or more (PD-L1 < 10% vs PD-L1 ≥ 10%; PFS: P = 0.529, OS: P = 0.568).

Conclusion: Chemotherapy containing bevacizumab can be considered as first-line therapy in metastatic CRC irrespective of PD-L1 expression.

根据程序性细胞死亡配体 1,对转移性结直肠癌患者进行含有贝伐珠单抗的化疗的疗效。
背景介绍贝伐单抗是一种抗血管内皮生长因子(VEGF)的单克隆抗体,可抑制血管生成并减少肿瘤生长。据报道,血清血管内皮生长因子-C、乳酸脱氢酶和炎症指标是贝伐珠单抗治疗的相关预测指标。目的:根据 PD-L1 的表达,研究转移性结直肠癌(CRC)患者接受含贝伐单抗化疗的疗效:这项分析包括2014年6月24日至2022年2月28日期间在三星医疗中心(韩国首尔)接受贝伐单抗联合FOLFOX或FOLFIRI一线治疗的CRC患者。患者数据分析包括通过联合阳性评分(CPS)评估PD-L1的表达。我们根据 PD-L1 表达状态分析了贝伐单抗对 CRC 患者的疗效:结果:共有124名患者参与了此次分析。几乎所有患者都接受了贝伐单抗联合 FOLFIRI 或 FOLFOX 作为一线化疗。77%的患者接受了FOLFOX,23%的患者接受了FOLFIRI作为骨干一线化疗。PD-L1 CPS 为 1 或以上、5 或以上或 10 或以上的患者人数分别为 105 人(85%)、64 人(52%)和 32 人(26%)。结果显示,PD-L1 CPS小于1和PD-L1 CPS大于或等于1的患者在贝伐珠单抗治疗下的无进展生存期(PFS)和总生存期(OS)无明显差异(PD-L1 < 1% vs PD-L1 ≥ 1%;PFS:P = 0.93,OS:P = 0.33),在PD-L1 CPS小于5和大于5的患者之间(PD-L1 < 5% vs PD-L1 ≥ 5%;PFS:P = 0.409,OS:P = 0.746),以及在PD-L1 CPS小于10和大于10的患者之间(PD-L1 < 10% vs PD-L1 ≥ 10%;PFS:P = 0.529,OS:P = 0.568):结论:无论PD-L1表达如何,含有贝伐珠单抗的化疗均可作为转移性CRC的一线疗法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
World Journal of Gastrointestinal Oncology
World Journal of Gastrointestinal Oncology Medicine-Gastroenterology
CiteScore
4.20
自引率
3.30%
发文量
1082
期刊介绍: The World Journal of Gastrointestinal Oncology (WJGO) is a leading academic journal devoted to reporting the latest, cutting-edge research progress and findings of basic research and clinical practice in the field of gastrointestinal oncology.
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