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阿帕替尼治疗不可切除或复发肝癌患者的疗效与安全性:一项回顾性研究。

The Efficacy and Safety of Apatinib Treatment for Patients with Unresectable or Relapsed Liver Cancer: a retrospective study.

作者信息

Zhen Liu, Jiali Chen, Yong Fang, Han Xufeng, Hongming Pan, Weidong Han

机构信息

Department of Medical Oncology, Sir Run Run Shaw Hospital, College of Medicine, Zhejiang University, Hangzhou, Zhejiang, China.

Department of Internal Medicine, Yuyao Traditional Chinese Medicine Hospital, Yuyao, Zhejiang, China.

出版信息

J Cancer. 2018 Jul 16;9(16):2773-2777. doi: 10.7150/jca.26376. eCollection 2018.

Abstract

Liver cancer is insensitive to chemotherapy. Sorafenib is currently the standard treatment for patients with advanced diseases, with mild survival extension and several intolerable drug-related side effects. The establishment of new treatments is an unmet clinical need. The aim of our study was to assess the efficacy and safety of apatinib, a novel antiangiogenic drug, in the treatment of patients with liver cancer. Patients with unresectable or relapsed liver cancer were included in a single center, retrospective, observational study and treated with apatinib until progressive disease or unacceptable toxicity. 32 patients were reviewed from January 2015 to March 2017. No complete response (CR) occurred, 5 patients (16%) showed partial response (PR), 14 patients (44%) had stable disease (SD), 13 patients (41%) had progressive disease (PD), with disease control rate of 60%. Median progression-free survival (PFS) was 5 months (95% confidence interval [CI]: 4.3-6.1 months) for hepatocellular carcinoma (HCC) and 3 months (95% CI: 2.5-4.2 months) for intrahepatic cholangiocarcinoma (ICC). The median overall survival (OS) was 13 months (95% CI: 12.4-14.1 months) for HCC and 5 months (95% CI: 4.5-6.2 months) for ICC, respectively. The most common adverse effects (AEs) were proteinuria (31%), secondary hypertension (28%) and liver dysfunction (13%). Apatinib treatment was an effective for patients with liver cancer. The toxicities were mild and tolerable.

摘要

肝癌对化疗不敏感。索拉非尼是目前晚期肝癌患者的标准治疗药物,其生存期延长有限且伴有多种难以耐受的药物相关副作用。新型治疗方法的开发是一项尚未满足的临床需求。我们研究的目的是评估新型抗血管生成药物阿帕替尼治疗肝癌患者的疗效和安全性。不可切除或复发的肝癌患者纳入一项单中心、回顾性观察性研究,并接受阿帕替尼治疗,直至疾病进展或出现不可接受的毒性反应。对2015年1月至2017年3月期间的32例患者进行了回顾性分析。未出现完全缓解(CR),5例患者(16%)出现部分缓解(PR),14例患者(44%)疾病稳定(SD),13例患者(41%)疾病进展(PD),疾病控制率为60%。肝细胞癌(HCC)的中位无进展生存期(PFS)为5个月(95%置信区间[CI]:4.3 - 6.1个月),肝内胆管癌(ICC)为3个月(95%CI:2.5 - 4.2个月)。HCC和ICC的中位总生存期(OS)分别为13个月(95%CI:12.4 - 14.1个月)和5个月(95%CI:4.5 - 6.2个月)。最常见的不良反应(AE)为蛋白尿(31%)、继发性高血压(28%)和肝功能不全(13%)。阿帕替尼治疗对肝癌患者有效。毒性反应轻微且可耐受。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7513/6096375/09d4fef884c1/jcav09p2773g001.jpg

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