Department of Hepatobiliary and Pancreatic Oncology, Osaka International Cancer Institute, Osaka 541-8567, Japan.
Department of Radiation Oncology, Osaka International Cancer Institute, Osaka 541-8567, Japan.
Curr Oncol. 2024 Mar 15;31(3):1543-1555. doi: 10.3390/curroncol31030117.
Various locoregional treatments for localized hepatocellular carcinoma (HCC) have been developed. This retrospective study investigated the safety and feasibility of combining on-demand selective locoregional treatment for residual lesions after tumor shrinkage (complete response [CR] oriented) or for solitary or few drug-resistant lesions (progressive disease (PD) salvage) with first-line atezolizumab plus bevacizumab (atezo/bev) for unresectable HCC. Twenty-nine patients with unresectable HCC were included. Fourteen locoregional treatments were performed (CR oriented, 7; PD salvage, 7) in ten patients in the combination-therapy group. All patients in the combination-therapy group successfully achieved a CR or PD salvage status after the planned locoregional treatment. The objective response rate of the combination-therapy group (80.0%) was higher than that of the atezo/bev alone group (21.1%; = 0.005). Progression-free survival (PFS) and overall survival (OS) were longer in the combination group (medians for PFS and OS not reached) than in the atezo/bev alone group (median PFS, 7.4 months; median OS, 19.8 months) (PFS, = 0.004; OS, < 0.001). The albumin-bilirubin score did not change, and no severe complications occurred after locoregional treatment. When performed in a minimally invasive manner, on-demand selective locoregional treatment combined with first-line atezo/bev could be safe and feasible for unresectable HCC.
各种局部区域治疗方法已被开发用于局部肝癌(HCC)。本回顾性研究调查了按需选择性局部区域治疗联合一线阿替利珠单抗加贝伐珠单抗(atezo/bev)用于不可切除 HCC 的安全性和可行性,这些局部区域治疗方法用于肿瘤缩小后的残留病变(完全缓解[CR]导向)或用于单发或少数耐药病变(进展性疾病[PD]挽救)。纳入了 29 例不可切除 HCC 患者。在联合治疗组的 10 例患者中进行了 14 次局部区域治疗(CR 导向,7 次;PD 挽救,7 次)。联合治疗组的所有患者在计划的局部区域治疗后均成功实现了 CR 或 PD 挽救状态。联合治疗组的客观缓解率(80.0%)高于阿替利珠单抗单药组(21.1%;=0.005)。联合治疗组的无进展生存期(PFS)和总生存期(OS)均长于阿替利珠单抗单药组(中位 PFS 未达到;中位 OS,19.8 个月)(PFS,=0.004;OS,<0.001)。白蛋白-胆红素评分无变化,局部区域治疗后未发生严重并发症。当以微创方式进行时,按需选择性局部区域治疗联合一线阿替利珠单抗加贝伐珠单抗对不可切除 HCC 可能是安全且可行的。