Palmer Mathias E, Gile Jennifer J, Storandt Michael H, Jin Zhaohui, Zemla Tyler J, Tran Nguyen H, Mahipal Amit
Department of Medicine, Mayo Clinic, Rochester, MN 55905, USA.
Department of Oncology, Mayo Clinic, Rochester, MN 55905, USA.
Cancers (Basel). 2023 Oct 6;15(19):4867. doi: 10.3390/cancers15194867.
Lenvatinib, a multikinase inhibitor, is an FDA-approved treatment for advanced hepatocellular carcinoma (HCC) in the first-line setting. Recent trial data have established atezolizumab plus bevacizumab as well as tremelimumab plus durvalumab as preferred first-line treatment options for advanced HCC. The role of lenvatinib following progression on immunotherapy in patients with advanced HCC remains unclear.
We conducted a multicentric, retrospective analysis of patients with advanced HCC diagnosed between 2010 and 2021 at the Mayo Clinic in Minnesota, Arizona, and Florida who received immunotherapy followed by lenvatinib. Median overall survival and progression-free survival analyses were performed using the Kaplan-Meier method, and responses were determined using RECIST 1.1. Adverse events were determined using CTCAE v 4.0.
We identified 53 patients with advanced HCC who received lenvatinib following progression on immunotherapy. Forty five (85%) patients had a Child Pugh class A at diagnosis, while 30 (58%) patients were still Child Pugh A at time of lenvatinib initiation. Lenvatinib was administered as a second-line treatment in 85% of the patients. The median PFS was 3.7 months (95% CI: 3.2-6.6), and the median OS from the time of lenvatinib initiation was 12.8 months (95% CI: 6.7-19.5). In patients with Child Pugh class A, the median OS and PFS was 14 and 5.2 months, respectively. Race, gender, and Child Pugh class was associated with OS on multivariate analysis.
Our study, using real-world data, suggests that patients benefit from treatment with lenvatinib following progression on immunotherapy in advanced HCC. The optimal sequencing of therapy for patients with advanced HCC following progression on immunotherapy remains unknown, and these results need to be validated in a clinical trial.
乐伐替尼是一种多激酶抑制剂,是美国食品药品监督管理局(FDA)批准的用于一线治疗晚期肝细胞癌(HCC)的药物。最近的试验数据已确定阿替利珠单抗联合贝伐单抗以及曲美木单抗联合度伐利尤单抗为晚期HCC的首选一线治疗方案。对于晚期HCC患者,免疫治疗进展后乐伐替尼的作用仍不清楚。
我们对2010年至2021年期间在明尼苏达州、亚利桑那州和佛罗里达州的梅奥诊所诊断为晚期HCC并接受免疫治疗后使用乐伐替尼的患者进行了多中心回顾性分析。采用Kaplan-Meier方法进行中位总生存期和无进展生存期分析,并使用RECIST 1.1确定反应。使用CTCAE v 4.0确定不良事件。
我们确定了53例晚期HCC患者,他们在免疫治疗进展后接受了乐伐替尼治疗。45例(85%)患者诊断时为Child Pugh A级,而30例(58%)患者在开始使用乐伐替尼时仍为Child Pugh A级。85%的患者将乐伐替尼作为二线治疗药物。中位无进展生存期为3.7个月(95%置信区间:3.2 - 6.6),从开始使用乐伐替尼起的中位总生存期为12.8个月(95%置信区间:6.7 - 19.5)。在Child Pugh A级患者中,中位总生存期和无进展生存期分别为14个月和5.2个月。多因素分析显示,种族、性别和Child Pugh分级与总生存期相关。
我们的研究使用真实世界数据表明,晚期HCC患者在免疫治疗进展后接受乐伐替尼治疗可从中获益。免疫治疗进展后晚期HCC患者的最佳治疗顺序仍不清楚,这些结果需要在临床试验中得到验证。