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在不可切除肝细胞癌患者中,乐伐替尼对比索拉非尼用于阿替利珠单抗联合贝伐单抗治疗进展后的二线治疗:一项来自韩国和日本的多中心回顾性研究

Lenvatinib versus sorafenib as second-line therapy following progression on atezolizumab-bevacizumab in patients with unresectable hepatocellular carcinoma: a multicenter retrospective study from Korea and Japan.

作者信息

Cheon Jaekyung, Shimose Shigeo, Kim Hyung-Don, Niizeki Takashi, Ryu Min-Hee, Shirono Tomotake, Ryoo Baek-Yeol, Iwamoto Hideki, Yoo Changhoon

机构信息

Department of Oncology, Asan Medical Center, University of Ulsan College of Medicine, 88, Olympic-ro 43-gil, Songpa-gu, Seoul, 05505, Republic of Korea.

Division of Gastroenterology, Department of Medicine, Kurume University School of Medicine, 67 Asahi-machi, Kurume, 830-0011, Japan.

出版信息

J Cancer Res Clin Oncol. 2025 Jan 28;151(2):52. doi: 10.1007/s00432-025-06085-1.

Abstract

PURPOSE

Atezolizumab-bevacizumab (AB) is the established first-line systemic therapy for patients with unresectable hepatocellular carcinoma (uHCC). However, the optimal second-line treatment for patients unresponsive to AB remains undefined.

PATIENTS AND METHODS

This multicenter, retrospective study included patients with uHCC who underwent second-line treatment with lenvatinib (LEN) or sorafenib (SOR) after AB failure at two academic centers between June 2018 and November 2023. Treatment response was assessed using Response Evaluation Criteria in Solid Tumors (RECIST) v1.1 and modified RECIST. Propensity score matching (PSM) was employed to mitigate confounding bias.

RESULTS

A total of 123 were included in the final analysis, 56 patients received LEN, and 67 received SOR. Before PSM, LEN was associated with significantly improved progression-free survival (PFS) compared with SOR (median 4.9 vs. 3.3 months, p < 0.001); however, no significant difference in overall survival (OS) was observed (median 13.2 vs. 11.5 months, p = 0.651). After PSM, in a cohort of 50 patients (25 per each group), LEN maintained its PFS advantage over SOR (median 4.8 vs. 3.3 months, p = 0.046), while the median OS was longer with LEN but not statistically different (median 11.4 vs. 7.9 months, p = 0.197). Response rates were 40% for LEN and 12% for SOR (p = 0.021) based on modified RECIST, and 12% and 8% (p = 0.728) based on RECIST v1.1, respectively.

CONCLUSION

In this real-world study, LEN demonstrated superior PFS and comparable OS to SOR as second-line treatment for uHCC after progression on AB.

摘要

目的

阿替利珠单抗-贝伐珠单抗(AB)是不可切除肝细胞癌(uHCC)患者既定的一线全身治疗方案。然而,对AB无反应的患者的最佳二线治疗方案仍未明确。

患者与方法

这项多中心回顾性研究纳入了2018年6月至2023年11月期间在两个学术中心AB治疗失败后接受乐伐替尼(LEN)或索拉非尼(SOR)二线治疗的uHCC患者。使用实体瘤疗效评价标准(RECIST)v1.1和改良RECIST评估治疗反应。采用倾向评分匹配(PSM)来减轻混杂偏倚。

结果

最终分析共纳入123例患者,56例患者接受LEN治疗,67例接受SOR治疗。在PSM之前,与SOR相比,LEN与无进展生存期(PFS)显著改善相关(中位值4.9个月对3.3个月,p < 0.001);然而,总生存期(OS)未观察到显著差异(中位值13.2个月对11.5个月,p = 0.651)。PSM后,在一组50例患者(每组25例)中,LEN相对于SOR保持其PFS优势(中位值4.8个月对3.3个月,p = 0.046),而LEN的中位OS更长,但无统计学差异(中位值11.4个月对7.9个月,p = 0.197)。基于改良RECIST,LEN的缓解率为40%,SOR为12%(p = 0.021),基于RECIST v1.1分别为12%和8%(p = 0.728)。

结论

在这项真实世界研究中,对于AB治疗进展后的uHCC患者,LEN作为二线治疗显示出优于SOR的PFS和相当的OS。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/89c0/11792941/0ca21d33a25f/432_2025_6085_Fig1_HTML.jpg

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