Sorafenib as Adjuvant Therapy Post-Liver Transplant: A Single-center Experience

被引:0
|
作者
Hassanain, Hala [1 ]
Connor, Ashton A. [1 ]
Brombosz, Elizabeth W. [1 ]
Patel, Khush [1 ]
Elaileh, Ahmed [1 ]
Basra, Tamneet [2 ]
Kodali, Sudha [2 ]
Victor, David W. [2 ]
Simon, Caroline J. [1 ]
Cheah, Yee Lee [1 ]
Hobeika, Mark J. [1 ]
Mobley, Constance M. [1 ]
Saharia, Ashish [1 ]
Dhingra, Sadhna [3 ]
Schwartz, Mary [3 ]
Maqsood, Anaum [4 ]
Heyne, Kirk [4 ]
Kaseb, Ahmed O. [5 ]
Vauthey, Jean-Nicolas [6 ]
Gaber, A. Osama [1 ]
Abdelrahim, Maen [4 ]
Ghobrial, R. Mark [1 ]
机构
[1] Houston Methodist Hosp, Dept Surg, 6550 Fannin St,SM 1661, Houston, TX 77030 USA
[2] Houston Methodist Hosp, Dept Med, Houston, TX USA
[3] Houston Methodist Hosp, Dept Pathol & Genom Med, Houston, TX USA
[4] Houston Methodist Hosp, Dr Mary & Ron Neal Canc Ctr, Dept Med, Houston, TX USA
[5] Univ Texas MD Anderson Canc Ctr, Dept Gastrointestinal Med Oncol, Div Canc Med, Houston, TX USA
[6] Univ Texas MD Anderson Canc Ctr, Dept Surg Oncol, Div Surg, Houston, TX USA
来源
TRANSPLANTATION DIRECT | 2025年 / 11卷 / 02期
关键词
HEPATOCELLULAR-CARCINOMA; RECURRENCE; RESECTION; EFFICACY; TRIAL;
D O I
10.1097/TXD.0000000000001746
中图分类号
R3 [基础医学]; R4 [临床医学];
学科分类号
1001 ; 1002 ; 100602 ;
摘要
Background. Hepatocellular carcinoma (HCC) has a rising incidence and mortality in North America. Liver transplantation (LT) with adjunctive therapies offers excellent outcomes. However, HCC recurrences are associated with high mortality. We investigate whether adjuvant systemic therapy can reduce recurrence, as shown with other malignancies. Methods. Medical records of patients undergoing LT for HCC at a single center between January 2016 and December 2022 were retrospectively reviewed. Patients were stratified into 3 groups: (1) recipients of adjuvant sorafenib, (2) nonrecipients at high recurrence risk, and (3) nonrecipients at low risk by explant pathology features. The outcomes were overall survival (OS) and recurrence-free survival (RFS). Adjuvant sorafenib recipients were also propensity score matched 1:2 to nonadjuvant recipients based on recurrence risk features. Results. During the study period, 273 patients with HCC underwent LT and 16 (5.9%) received adjuvant sorafenib therapy. Adjuvant sorafenib recipients were demographically similar to nonrecipients and, on explant pathology, had greater tumor burden, lymphovascular invasion, and poorer differentiation (all P < 0.001). Adverse events were observed in 12 adjuvant sorafenib recipients (75%). OS was similar among the 3 groups (P = 0.2), and adjuvant sorafenib was not associated with OS in multivariable analysis (hazard ratio, 1.31; 95% confidence interval, 0.45-3.78; P = 0.62). RFS was significantly lower in sorafenib patients (hazard ratio, 6.99; 95% confidence interval, 2.12-23.05; P = 0.001). Following propensity matching, adjuvant sorafenib use was not associated with either OS (P = 0.24) or RFS rates (P = 0.65). Conclusions. In this single-center analysis, adjuvant sorafenib was not associated with OS. Recipients were observed to have shorter RFS, likely due to the increased prevalence of high-risk features, and sorafenib use was associated with high frequencies of adverse events.
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页数:7
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