Oranratnachai Songporn, Rattanasiri Sasivimol, Pooprasert Anantaporn, Tansawet Amarit, Reungwetwattana Thanyanan, Attia John, Thakkinstian Ammarin
Department of Clinical Epidemiology and Biostatistics, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.
Oncology Clinic, Sriphat Medical Center, Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand.
Front Oncol. 2021 Mar 31;11:654020. doi: 10.3389/fonc.2021.654020. eCollection 2021.
Hepatocellular carcinoma (HCC) is the third most fatal cancer, with a 5-year survival rate of 18%. Standard frontline-therapy is multikinase inhibitors (MKIs), but accessibility is still limited, particularly in developing countries. This network meta-analysis (NMA) aimed to compare the efficacy of usual chemotherapy vs MKIs.
Randomised-controlled trials (RCTs) comparing any among chemotherapy vs MKIs in treatment-naïve patients with advanced HCCs were identified from MEDLINE and SCOPUS databases. Overall survival (OS) and progression-free survival (PFS) probabilities and times were extracted from Kaplan-Meier curves using Digitizer, and then converted to individual patient time-to-event data. A one-stage mixed-effect survival model was applied to estimate median OS and PFS. A two-stage NMA was applied for the overall response rate and adverse events (AEs) outcome.
A total of 20 RCTs were eligible for NMA. Lenvatinib was the best treatment among single MKIs, with median OS and PFS of 9 and 6.3 months, without significant differences in AEs relative to other MKIs. Median OS and PFS were 0.70 (-0.42, 1.83) and 2.17 (1.41, 2.93) months longer with Lenvatinib than Sorafenib. Among chemotherapy agents, FOLFOX4 had the longest median OS and PFS at 7.9 and 4.3 months, respectively, without significant AEs compared to other chemotherapies. The combination of Sorafenib+Doxorubicin prolonged median OS and PFS to 12.7 and 6.3 months, respectively.
Use of the MKIs Lenvatinib or Sorafenib as first line systemic treatment for advanced HCC could be beneficial. However, FOLFOX4 might be the optimal choice in a developing country where the health-care budget is limited.
肝细胞癌(HCC)是第三大致命性癌症,5年生存率为18%。标准一线治疗是多激酶抑制剂(MKIs),但其可及性仍然有限,尤其是在发展中国家。这项网络荟萃分析(NMA)旨在比较常规化疗与MKIs的疗效。
从MEDLINE和SCOPUS数据库中识别出比较初治晚期HCC患者化疗与MKIs中任何一种的随机对照试验(RCTs)。使用Digitizer从Kaplan-Meier曲线中提取总生存期(OS)和无进展生存期(PFS)概率及时间,然后转换为个体患者的事件发生时间数据。应用单阶段混合效应生存模型来估计中位OS和PFS。应用两阶段NMA来分析总缓解率和不良事件(AEs)结果。
共有20项RCTs符合NMA纳入标准。乐伐替尼是单一MKIs中最佳治疗药物,中位OS和PFS分别为9个月和6.3个月,与其他MKIs相比,AEs无显著差异。乐伐替尼的中位OS和PFS比索拉非尼分别长0.70(-0.42,1.83)个月和2.17(1.41,2.93)个月。在化疗药物中,FOLFOX4的中位OS和PFS最长,分别为7.9个月和4.3个月,与其他化疗相比,AEs无显著差异。索拉非尼+阿霉素联合方案将中位OS和PFS分别延长至12.7个月和6.3个月。
使用MKIs乐伐替尼或索拉非尼作为晚期HCC的一线全身治疗可能有益。然而,在医疗保健预算有限的发展中国家FOLFOX4可能是最佳选择。