Ma Kun-Peng, Fu Jin-Xin, Duan Feng, Wang Mao-Qiang
Department of Interventional Radiology, The Fifth Medical Center of Chinese People's Liberation Army General Hospital, Beijing 100853, China.
Chinese People's Liberation Army Medical School, Beijing 100853, China.
World J Gastrointest Oncol. 2024 Apr 15;16(4):1236-1247. doi: 10.4251/wjgo.v16.i4.1236.
The efficacy and safety of transarterial chemoembolization (TACE) combined with lenvatinib plus programmed cell death protein-1 (PD-1) for unresectable hepatocellular carcinoma (HCC) have rarely been evaluated and it is unknown which factors are related to efficacy.
To evaluate the efficacy and independent predictive factors of TACE combined with lenvatinib plus PD-1 inhibitors for unresectable HCC.
This study retrospectively enrolled patients with unresectable HCC who received TACE/lenvatinib/PD-1 treatment between March 2019 and April 2022. Overall survival (OS) and progression-free survival (PFS) were determined. The objective response rate (ORR) and disease control rate (DCR) were evaluated in accordance with the modified Response Evaluation Criteria in Solid Tumors. Additionally, the prognostic factors affecting the clinical outcome were assessed.
One hundred and two patients were enrolled with a median follow-up duration of 12.63 months. The median OS was 26.43 months (95%CI: 17.00-35.87), and the median PFS was 10.07 months (95%CI: 8.50-11.65). The ORR and DCR were 61.76% and 81.37%, respectively. The patients with Barcelona Clinic Liver Cancer Classification (BCLC) B stage, early neutrophil-to-lymphocyte ratio (NLR) response (decrease), or early alpha-fetoprotein (AFP) response (decrease > 20%) had superior OS and PFS than their counterparts.
This study showed that TACE/lenvatinib/PD-1 treatment was well tolerated with encouraging efficacy in patients with unresectable HCC. The patients with BCLC B-stage disease with early NLR response (decrease) and early AFP response (decrease > 20%) may achieve better clinical outcomes with this triple therapy.
经动脉化疗栓塞术(TACE)联合乐伐替尼及程序性细胞死亡蛋白1(PD-1)治疗不可切除肝细胞癌(HCC)的疗效和安全性鲜有评估,且尚不清楚哪些因素与疗效相关。
评估TACE联合乐伐替尼及PD-1抑制剂治疗不可切除HCC的疗效及独立预测因素。
本研究回顾性纳入了2019年3月至2022年4月期间接受TACE/乐伐替尼/PD-1治疗的不可切除HCC患者。测定总生存期(OS)和无进展生存期(PFS)。根据改良的实体瘤疗效评价标准评估客观缓解率(ORR)和疾病控制率(DCR)。此外,评估影响临床结局的预后因素。
共纳入102例患者,中位随访时间为12.63个月。中位OS为26.43个月(95%CI:17.00-35.87),中位PFS为10.07个月(95%CI:8.50-11.65)。ORR和DCR分别为61.76%和81.37%。巴塞罗那临床肝癌分期(BCLC)为B期、中性粒细胞与淋巴细胞比值(NLR)早期有反应(降低)或甲胎蛋白(AFP)早期有反应(降低>20%)的患者,其OS和PFS优于相应患者。
本研究表明,TACE/乐伐替尼/PD-1治疗对不可切除HCC患者耐受性良好,疗效令人鼓舞。BCLC B期疾病、NLR早期有反应(降低)和AFP早期有反应(降低>20%)的患者接受这种三联疗法可能获得更好的临床结局。