Barcelona Clinic Liver Cancer (BCLC) Group, Liver Unit, Hospital Clínic de Barcelona, IDIBAPS, Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBERehd), Universidad de Barcelona, Barcelona, Spain.
Medical Statistics Core Facility, IDIBAPS, Hospital Clinic Barcelona & Biostatistics Unit, Faculty of Medicine, Universitat Autònoma de Barcelona, Barcelona, Spain.
Aliment Pharmacol Ther. 2019 Mar;49(5):482-491. doi: 10.1111/apt.15088. Epub 2019 Jan 29.
The positive results of the REFLECT trial in terms of survival (sorafenib vs lenvatinib) offer a new first-line option for hepatocellular carcinoma. Additionally, the expected results of immunotherapy could change the first-line treatment in hepatocellular carcinoma or the clinical trial design in first and second-line.
To evaluate the impact of dermatologic adverse events under sorafenib in hepatocellular carcinoma patients as a clinical marker to predict prognosis and critically evaluate outcomes within trials.
A systematic search of original articles published until October 2018 was performed using PubMed/MEDLINE and a meta-analysis was performed according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) statement.
A total of 393 studies were identified and 13 articles with 2035 patients (79.5% Child-Pugh-A, 73.2% BCLC-C) were selected for qualitative and quantitative analysis. The main type of dermatologic adverse events was hand-foot skin reaction (47.7%) but other dermatologic adverse events were reported in 31.7% of the cases. Presence of dermatologic adverse events was associated with a lower mortality when compared with those patients without them (pooled Hazard Ratio for the univariate analysis 0.45 (95% CI: 0.38-0.53) and there was no heterogeneity for the analysis (P = 0.511; I = 0.0%). Refuting this association would require the future report of 1370 negative studies.
This meta-analysis shows a clinically meaningful association between dermatologic adverse events and a higher probability of longer survival. These data support the use of dermatologic adverse events in the clinical decision-making when informing the prognosis and when systemic treatment is decided.
REFLECT 试验在生存方面(索拉非尼与仑伐替尼)的积极结果为肝细胞癌提供了新的一线治疗选择。此外,免疫疗法的预期结果可能会改变肝细胞癌的一线治疗或一线和二线临床试验的设计。
评估索拉非尼治疗肝细胞癌患者的皮肤不良反应对预测预后的临床意义,并对临床试验结果进行批判性评估。
使用 PubMed/MEDLINE 进行系统检索,直到 2018 年 10 月发表的原始文章,并根据系统评价和荟萃分析的首选报告项目(PRISMA)声明进行荟萃分析。
共确定了 393 项研究,纳入了 13 项包含 2035 例患者(79.5%Child-Pugh-A,73.2%BCLC-C)的文章进行定性和定量分析。主要的皮肤不良反应类型是手足皮肤反应(47.7%),但其他皮肤不良反应在 31.7%的病例中也有报道。与无皮肤不良反应的患者相比,出现皮肤不良反应的患者死亡率较低(单变量分析的合并危险比为 0.45(95%CI:0.38-0.53),分析无异质性(P=0.511;I²=0.0%)。要反驳这种关联,需要未来报告 1370 项阴性研究。
这项荟萃分析显示皮肤不良反应与更高的生存率之间存在临床意义上的关联。这些数据支持在临床决策中使用皮肤不良反应来告知预后和决定系统治疗时。