The Outcomes of Systemic Treatment in Recurrent Hepatocellular Carcinomas Following Liver Transplants

医学 肝细胞癌 索拉非尼 内科学 危险系数 胃肠病学 肝移植 不利影响 外科 比例危险模型 米兰标准 移植 置信区间
作者
Bryan Cho Wing Li,Joanne Wing Yan Chiu,Kit Shing,Gerry Gin Wai Kwok,Vikki Tang,Roland Leung,Ka Wing,Wong Hoi She,Josephine Tsang,Albert C. Y. Chan,Tan To Cheung,Chung Mau Lo,Thomas Yau
出处
期刊:Advances in Therapy [Adis, Springer Healthcare]
卷期号:38 (7): 3900-3910 被引量:8
标识
DOI:10.1007/s12325-021-01800-z
摘要

Treatment of hepatocellular carcinoma (HCC) recurrences following liver transplant (LT) is challenging. Most clinical trials of systemic therapies for advanced HCC excluded patients with any history of organ transplant. We aimed to assess the outcomes in using various systemic therapies in patients with post-LT recurrence. Consecutive patients with HCC and recurrences following LT at a large tertiary centre from 2005 to 2018 were reviewed. Overall survival (OS), response rates and adverse events (AEs) were analysed. Forty-three consecutive patients with a recurrence of HCC following LT were identified from 2005 to 2018. Median OS from diagnosis of recurrence was 17 months (CI 11.3, 22.7). Early recurrence within 12 months of transplant was associated with a significantly worse median survival of 10 months (CI 8.5, 11.4) compared to 26 months (CI 18.8, 33.2) when recurrences occurred after 12 months from transplant (p < 0.001) with a hazard ratio of 0.104 (log-rank test, p < 0.001). A total of 41 patients had received systemic therapies and 79.1% of them were on sorafenib as the first-line treatment. Among these patients treated with sorafenib, median OS from recurrence was 14 months (CI 7.3, 20.7). Hand-foot syndrome (34.7%) was most common among AEs followed by diarrhoea (26.7%). Overall, AEs led to dose interruptions in 8.8% of patients. Notably, 47.1% of patients received subsequent lines of systemic therapies after sorafenib. Early recurrence within 1 year from transplant was the most significant risk factor. Treatment efficacy and adverse events and tolerability of sorafenib were comparable with those in the setting of advanced HCC without transplant.

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