Jiang Yi, Su Ke, Li Han, Wang Chenjie, Wu Zhenying, Chen Jiali, Zhang Zhiyao, He Kun, Han Yunwei
Department of Oncology, The Affiliated Hospital of Southwest Medical University, 25 Taiping Street, Luzhou City, Sichuan Province, 646000, China.
Department of Radiation Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100000, China.
Invest New Drugs. 2025 Feb;43(1):18-29. doi: 10.1007/s10637-024-01468-6. Epub 2024 Dec 17.
Currently, therapeutic combinations of immune checkpoint inhibitors (ICIs) with anti-angiogenic agents have shown promising outcomes and have the potential to establish a new standard of care. The efficacy and safety of the first-line combination of envafolimab (an ICI) and lenvatinib (an anti-tumor angiogenesis drug) for the treatment of patients with inoperable hepatocellular carcinoma (HCC) have not been demonstrated. Unresectable HCC patients with an Eastern Cooperative Oncology Group (ECOG) physical status score ≤ 1 and a Child-Pugh score ≤ 7 who had not received systemic therapy were included in this single-arm, exploratory, multicentre phase II clinical study. All patients were required to meet the criteria of being at least 18 years of age, having no history of other malignancies, and existing at least one measurable lesion. The patients were treated with envafolimab (150 mg, QW, subcutaneous) in combination with lenvatinib (12 mg for patients weighing over 60 kg, 8 mg for patients weighing under 60 kg). The co-primary endpoint of the study was overall survival (OS), while surrogate endpoints included progression-free survival (PFS), objective response rate (ORR), disease control rate (DCR), and safety. Between March 2022 and April 2023, 36 patients were enrolled, 30 of whom were treated with envafolimab plus lenvatinib. At data cutoff, the median follow-up duration was 20 months (95% CI 18.9-21.1). Among the 30 assessable patients (patients treated according to the trial protocol), the median overall survival (mOS) and median progression-free survival (mPFS) for the therapy comprising envafolimab alongside lenvatinib were 18.5 months (95% CI 13.2-23.8) and 9.4 months (95% CI 1.6-15.6), respectively. The ORR and the DCR (evaluated according to mRECIST criteria) reached 40% and 80%, respectively. In terms of safety, 23 patients (76.7%) experienced at least one treatment-related adverse event (TRAE), of which the most common was elevated aspartate aminotransferase (AST, 23.3%). Furthermore, grade 3 and higher TRAEs occurred in 30%. This study demonstrates that envafolimab in combination with lenvatinib exhibits favourable anti-cancer activity and a manageable safety profile for the first-line treatment of patients with unresectable HCC.
目前,免疫检查点抑制剂(ICI)与抗血管生成药物的联合治疗已显示出有前景的结果,并有可能确立新的治疗标准。恩沃利单抗(一种ICI)和仑伐替尼(一种抗肿瘤血管生成药物)一线联合治疗不可切除肝细胞癌(HCC)患者的疗效和安全性尚未得到证实。本单臂、探索性、多中心II期临床研究纳入了东部肿瘤协作组(ECOG)体能状态评分≤1且Child-Pugh评分≤7、未接受过全身治疗的不可切除HCC患者。所有患者均需满足年龄至少18岁、无其他恶性肿瘤病史且至少存在一个可测量病灶的标准。患者接受恩沃利单抗(150 mg,每周一次,皮下注射)联合仑伐替尼(体重超过60 kg的患者12 mg,体重低于60 kg的患者8 mg)治疗。该研究的共同主要终点为总生存期(OS),替代终点包括无进展生存期(PFS)、客观缓解率(ORR)、疾病控制率(DCR)和安全性。2022年3月至2023年4月期间,共纳入36例患者,其中30例接受了恩沃利单抗加仑伐替尼治疗。在数据截止时,中位随访时间为20个月(95%CI 18.9-21.1)。在30例可评估患者(按试验方案治疗的患者)中,恩沃利单抗联合仑伐替尼治疗的中位总生存期(mOS)和中位无进展生存期(mPFS)分别为18.5个月(95%CI 13.2-23.8)和9.4个月(95%CI 1.6-15.6)。ORR和DCR(根据mRECIST标准评估)分别达到40%和80%。在安全性方面,23例患者(76.7%)经历了至少一次治疗相关不良事件(TRAE),其中最常见的是天门冬氨酸氨基转移酶(AST)升高(23.3%)。此外,3级及以上TRAE的发生率为30%。本研究表明,恩沃利单抗联合仑伐替尼对不可切除HCC患者的一线治疗具有良好的抗癌活性和可控的安全性。