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乐伐替尼联合PD-1抑制剂与瑞戈非尼治疗索拉非尼治疗失败后的晚期肝细胞癌患者的回顾性研究

Lenvatinib Plus PD-1 Inhibitors versus Regorafenib in Patients with Advanced Hepatocellular Carcinoma After the Failure of Sorafenib: A Retrospective Study.

作者信息

Xu Yongkang, Fu Shumin, Liu Kan, Mao Ye, Wu Jianbing

机构信息

Department of Oncology, The Second Affiliated Hospital of Nanchang University, Nanchang, People's Republic of China.

出版信息

Ther Clin Risk Manag. 2023 Oct 24;19:853-863. doi: 10.2147/TCRM.S420371. eCollection 2023.

Abstract

PURPOSE

To evaluate the clinical outcomes of lenvatinib plus PD-1 inhibitors (LP) and regorafenib (R) in patients with advanced hepatocellular carcinoma (HCC) after sorafenib failure.

METHODS

From June 2018 to September 2021, 68 patients from a single center who received lenvatinib combined with PD-1 inhibitors or regorafenib after sorafenib treatment failure were analyzed. The tumor response and survival outcomes were compared between the LP group and R group. Prognostic factors for OS and PFS were determined using Cox proportional hazard regression models.

RESULTS

The ORR increased in the LP group (19.5% vs 7.4%, p =0.294), and the DCR was better in the R group (73.2% vs 44.4%, p =0.017). Additionally, median PFS and OS were not significantly different between the LP group and R two groups in survival analysis (PFS: 5.3 months vs 3.0 months, p =0.633; OS: 11.8 months vs 8.0 months, p =0.699). The common adverse events (≥grade 3) were hand-foot skin reactions (13.1%). In multivariate analyses, AFP≥400 ng/mL and ECOG PS 2 were independent risk factors for poor prognosis.

CONCLUSION

The LP group appeared to have a trend of greater tumor response and a higher disease control rate than the R group among patients with sorafenib-resistant HCC, although PFS and OS did not differ significantly between the two groups.

摘要

目的

评估乐伐替尼联合PD - 1抑制剂(LP)和瑞戈非尼(R)用于索拉非尼治疗失败的晚期肝细胞癌(HCC)患者的临床疗效。

方法

对2018年6月至2021年9月间来自单一中心的68例索拉非尼治疗失败后接受乐伐替尼联合PD - 1抑制剂或瑞戈非尼治疗的患者进行分析。比较LP组和R组的肿瘤反应及生存结局。采用Cox比例风险回归模型确定总生存期(OS)和无进展生存期(PFS)的预后因素。

结果

LP组的客观缓解率(ORR)有所升高(19.5%对7.4%,p = 0.294),R组的疾病控制率(DCR)更高(73.2%对44.4%,p = 0.017)。此外,生存分析中LP组和R组的中位PFS和OS无显著差异(PFS:5.3个月对3.0个月,p = 0.633;OS:11.8个月对8.0个月,p = 0.699)。常见的≥3级不良事件为手足皮肤反应(13.1%)。多因素分析中,甲胎蛋白(AFP)≥400 ng/mL和东部肿瘤协作组(ECOG)体能状态评分为2是预后不良的独立危险因素。

结论

在索拉非尼耐药的HCC患者中,LP组似乎比R组有更高的肿瘤反应趋势和疾病控制率,尽管两组之间的PFS和OS无显著差异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c90/10612499/8463cf31d553/TCRM-19-853-g0001.jpg

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