Ren Yupeng, Li Yuxuan, Cao Mingbo, Tang Yongchang, Yuan Feng, Yang Gaoyuan, He Zhiwei, Shi Zheng, Su Xiaorui, Yao Zhicheng, Deng Meihai
Department of Hepatobiliary Surgery, the Third Affiliated Hospital, Sun Yat-sen University, Guangzhou 510630, China.
Department of General Surgery, Qilu Hospital, Shandong University, Jinan 250012, China.
Chin J Cancer Res. 2024 Apr 30;36(2):114-123. doi: 10.21147/j.issn.1000-9604.2024.02.02.
Unresectable hepatocellular carcinoma (uHCC) continues to pose effective treatment options. The objective of this study was to assess the efficacy and safety of combining low-dose cyclophosphamide with lenvatinib, pembrolizumab and transarterial chemoembolization (TACE) for the treatment of uHCC.
From February 2022 to November 2023, a total of 40 patients diagnosed with uHCC were enrolled in this small-dose, single-center, single-arm, prospective study. They received a combined treatment of low-dose cyclophosphamide with lenvatinib, pembrolizumab, and TACE. Study endpoints included progression-free survival (PFS), objective response rate (ORR), and safety assessment. Tumor response was assessed using the modified Response Evaluation Criteria in Solid Tumors (mRECIST), while survival analysis was conducted through Kaplan-Meier curve analysis for overall survival (OS) and PFS. Adverse events (AEs) were evaluated according to the National Cancer Institute Common Terminology Criteria for Adverse Events (version 5.0).
A total of 34 patients were included in the study. The median follow-up duration was 11.2 [95% confidence interval (95% CI), 5.3-14.6] months, and the median PFS (mPFS) was 15.5 (95% CI, 5.4-NA) months. Median OS (mOS) was not attained during the study period. The ORR was 55.9%, and the disease control rate (DCR) was 70.6%. AEs were reported in 27 (79.4%) patients. The most frequently reported AEs (with an incidence rate >10%) included abnormal liver function (52.9%), abdominal pain (44.1%), abdominal distension and constipation (29.4%), hypertension (20.6%), leukopenia (17.6%), constipation (17.6%), ascites (14.7%), and insomnia (14.7%). Abnormal liver function (14.7%) had the most common grade 3 or higher AEs.
A combination of low-dose cyclophosphamide with lenvatinib, pembrolizumab, and TACE is safe and effective for uHCC, showcasing a promising therapeutic strategy for managing uHCC.
不可切除肝细胞癌(uHCC)仍然缺乏有效的治疗选择。本研究的目的是评估低剂量环磷酰胺联合乐伐替尼、帕博利珠单抗和经动脉化疗栓塞术(TACE)治疗uHCC的疗效和安全性。
2022年2月至2023年11月,共有40例诊断为uHCC的患者纳入这项小剂量、单中心、单臂前瞻性研究。他们接受了低剂量环磷酰胺联合乐伐替尼、帕博利珠单抗和TACE的联合治疗。研究终点包括无进展生存期(PFS)、客观缓解率(ORR)和安全性评估。使用改良的实体瘤疗效评价标准(mRECIST)评估肿瘤反应,通过Kaplan-Meier曲线分析进行总生存期(OS)和PFS的生存分析。根据美国国立癌症研究所不良事件通用术语标准(第5.0版)评估不良事件(AE)。
共有34例患者纳入研究。中位随访时间为11.2[95%置信区间(95%CI),5.3 - 14.6]个月,中位PFS(mPFS)为15.5(95%CI,5.4 - NA)个月。研究期间未达到中位总生存期(mOS)。ORR为55.9%,疾病控制率(DCR)为70.6%。27例(79.4%)患者报告了AE。最常报告的AE(发生率>10%)包括肝功能异常(52.9%)、腹痛(44.1%)、腹胀和便秘(29.4%)、高血压(20.6%)、白细胞减少(17.6%)、便秘(17.6%)、腹水(14.7%)和失眠(14.7%)。肝功能异常(14.7%)是最常见的3级或更高等级AE。
低剂量环磷酰胺联合乐伐替尼、帕博利珠单抗和TACE治疗uHCC安全有效,为uHCC的治疗展示了一种有前景的治疗策略。