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索拉非尼、仑伐替尼作为伴门静脉癌栓的晚期肝细胞癌一线治疗药物。

Sorafenib . Lenvatinib as First-line Therapy for Advanced Hepatocellular Carcinoma With Portal Vein Tumor Thrombosis.

机构信息

Department of Gastroenterology and Hepatology, Nagoya University Graduate School of Medicine, Nagoya, Japan

Department of Gastroenterology and Hepatology, Nagoya University Graduate School of Medicine, Nagoya, Japan.

出版信息

Anticancer Res. 2020 Apr;40(4):2283-2290. doi: 10.21873/anticanres.14193.

DOI:10.21873/anticanres.14193
PMID:32234927
Abstract

BACKGROUND/AIM: We aimed to compare the outcomes between sorafenib and lenvatinib as first-line therapy for advanced hepatocellular carcinoma (HCC) with major portal vein tumor thrombosis (Vp3/4).

PATIENTS AND METHODS

This retrospective study enrolled 41 HCC patients with Vp3/4 and Child-Pugh A.

RESULTS

The outcomes in the lenvatinib group (n=13) were significantly better than those in the sorafenib group (n=28) [best objective response rate according to the modified Response Evaluation Criteria in Solid Tumors: 53.8% vs. 14.3%; p=0.0193, best disease control rate: 92.3% vs. 35.7%; p=0.0008, median overall survival (OS): not reached vs. 187 days; p=0.0040, respectively]. Lenvatinib treatment was the only significant predictor of better OS and time to tumor progression. No patient needed to discontinue lenvatinib treatment due to drug-related adverse events.

CONCLUSION

Compared with sorafenib, lenvatinib treatment for advanced HCC with Vp3/4 may lead to more favorable outcomes.

摘要

背景/目的:我们旨在比较索拉非尼和仑伐替尼作为伴有主门静脉癌栓(Vp3/4)的晚期肝细胞癌(HCC)一线治疗的疗效。

患者和方法

本回顾性研究纳入了 41 例伴有 Vp3/4 和 Child-Pugh A 的 HCC 患者。

结果

仑伐替尼组(n=13)的结果明显优于索拉非尼组(n=28)[根据实体瘤反应评价标准的改良版,最佳客观缓解率:53.8%比 14.3%;p=0.0193,最佳疾病控制率:92.3%比 35.7%;p=0.0008,中位总生存期(OS):未达到比 187 天;p=0.0040]。仑伐替尼治疗是 OS 和肿瘤进展时间更好的唯一显著预测因素。没有患者因药物相关不良反应而需要停止仑伐替尼治疗。

结论

与索拉非尼相比,仑伐替尼治疗伴有 Vp3/4 的晚期 HCC 可能会带来更有利的结果。

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