索拉非尼治疗肝癌:在现实世界环境中的结果

J. Parada, M. Gomariz, Á. P. Pérez, Cátia Jesus
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摘要

背景和重要性肝癌(HCC)是肝硬化患者死亡的主要原因。索拉非尼已被证明可提高生存率,并被认为是晚期不可切除HCC患者的一线治疗,这些患者不适合局部治疗,肝功能足以耐受治疗(Child Pugh A/B)。本研究的目的是基于总生存期(OS)和不良事件报告,在临床实践中评估索拉非尼治疗成人转移性HCC的有效性和安全性。材料与方法2018年1月至2020年10月进行了一项观察性、回顾性、描述性研究。从我们的电子记录中收集年龄、性别、巴塞罗那临床肝癌(BCLC)分期、不良事件(ae)、需要减少剂量或停药、进展或死亡时间。所有患者此前均未接受过全身治疗。采用r4.0.3进行分析。结果47例转移性HCC患者接受索拉非尼治疗。患者特征见表1。中位总生存期(mOS)为17.9个月(范围0.5-24.0;95% CI 15.5至未达到)。观察到的主要不良反应为:疲劳(42.5%)、手足皮肤反应(42.5%)、厌食(40.4%)、腹泻(38.3%)、高血压(14.9%)、腹痛(14.9%)、消化性出血(12.7%)和瘙痒(10.6%)。最常见的停药原因是不良事件(14例)和进展(22例)。ae导致的停药率为29.8%。34例(72.3%)患者需要减量。结论和相关性在我们的研究中,即使基线特征相似,mOS也优于关键临床试验中报告的结果。一些不良反应更为频繁,如疲劳、手足皮肤反应、高血压和厌食症,尽管因不良反应而停药的比率低于SHARP试验中报道的。Llovet JM, Ricci S, Mazzaferro V等。夏普调查员研究组。索拉非尼治疗晚期肝细胞癌。中华医学杂志,2008;39(1):387 - 398。doi: 10.1056 / NEJMoa0708857。PMID: 18650514。利益冲突无利益冲突
本文章由计算机程序翻译,如有差异,请以英文原文为准。
4CPS-302 Sorafenib in hepatocarcinoma: results in a real world setting
Background and importance Hepatocarcinoma (HCC) is the leading cause of mortality in cirrhotic patients. Sorafenib has been shown to increase survival and is considered firstline therapy for patients with advanced unresectable HCC who are unsuitable for locoregional therapy and whose liver function is adequate to tolerate therapy (Child Pugh A/B). Aim and objectives The aim of this study was to evaluate the effectiveness and safety of sorafenib in adults with metastatic HCC in our clinical practice, based on overall survival (OS) and report of adverse events. Material and methods An observational, retrospective, descriptive study was conducted between January 2018 and October 2020. Age, sex, Barcelona Clinic Liver Cancer (BCLC) staging, adverse events (AEs), need for dose reduction or discontinuation, and time to progression or death were collected from our electronic records. None of the patients had received previous systemic therapy. The analysis was performed using R 4.0.3. Results 47 patients with metastatic HCC were treated with sorafenib. Patient characteristics are shown in table 1. Median overall survival (mOS) was 17.9 months (range 0.5–24.0; 95% CI 15.5 to not reached). The main AEs observed were: fatigue (42.5%), hand–foot skin reactions (42.5%), anorexia (40.4%), diarrhoea (38.3%), hypertension (14.9%), abdominal pain (14.9%), digestive bleeding (12.7%) and pruritus (10.6%). The most common reasons for treatment discontinuation were AEs (14 patients) and progression (22 patients). The rate of discontinuation due to AEs was 29.8%. 34 patients (72.3%) required dose reduction. Conclusion and relevance In our setting, mOS was superior to that reported in the pivotal clinical trial even though baseline characteristics were similar. Some of the AEs were more frequent, such as fatigue, hand–foot skin reactions, hypertension and anorexia, although the rate of discontinuation due to AEs was lower than reported in the SHARP trial. References and/or acknowledgements Llovet JM, Ricci S, Mazzaferro V, et al. SHARP Investigators Study Group. Sorafenib in advanced hepatocellular carcinoma. N Engl J Med 2008;359:378–90. doi: 10.1056/NEJMoa0708857. PMID: 18650514. Conflict of interest No conflict of interest
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