病理完全缓解作为桥接治疗的预后指标:对肝细胞癌和肝移植结果的25年回顾性研究。

IF 0.8
Cihan Agalar, Tufan Egeli, Mucahit Ozbilgin, Berkay Sakaoglu, Anil Aysal, Ibrahim Astarcioglu, Aytac Gulcu, Nilay Danis, Erkan Derebek, Ozgul Sagol, Tarkan Unek
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引用次数: 0

摘要

目的:肝细胞癌(HCC)是癌症相关死亡的主要原因,肝移植(LT)仍然是符合条件的患者最有效的治疗选择。在等待期通常采用桥接疗法来控制肿瘤进展和提高移植资格。然而,它们的预后影响仍然存在争议。我们旨在评估桥接治疗和病理完全缓解(CR)对肝细胞癌肝移植患者移植后预后的影响。患者和方法:在这项回顾性研究中,对1998年至2023年间接受肝移植的120例HCC患者进行了分析。桥接治疗包括经动脉化疗栓塞(TACE)、经动脉放射栓塞(TARE)、射频消融(RFA)和微波消融(MWA)。比较接受和未接受桥接治疗的患者的总生存期(OS)、无病生存期(DFS)和复发率。同时评估病理性CR的预后意义。结果:接受桥接治疗的患者占24.2%。接受桥接治疗的患者与未接受桥接治疗的患者的OS或DFS无统计学差异。然而,27.6%的桥接患者达到病理性CR,并与改善的OS (P = 0.018)和DFS (P = 0.05)显著相关。达到cr的患者无复发或死亡发生。结论:虽然桥接治疗不单独影响移植后生存,但达到病理完全缓解是一个强有力的预后指标。这些发现强调了治疗反应的临床重要性,并支持CR作为HCC患者肝移植后有利长期预后的潜在预测因子的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pathologic Complete Response as a Prognostic Indicator in Bridging Therapy: A 25-Year Retrospective Study on Hepatocellular Carcinoma and Liver Transplantation Outcomes.

Aim: Hepatocellular carcinoma (HCC) is a leading cause of cancer-related mortality, and liver transplantation (LT) remains the most effective curative option for eligible patients. Bridging therapies are often employed during the waiting period to control tumor progression and improve transplant eligibility. However, their prognostic impact remains controversial. We aimed to evaluate the effect of bridging therapy and pathological complete response (CR) on post-transplant outcomes in patients who underwent LT for HCC.

Patients and methods: In this retrospective study, 120 patients with HCC who underwent LT between 1998 and 2023 were analyzed. Bridging therapies included transarterial chemoembolization (TACE), transarterial radioembolization (TARE), radiofrequency ablation (RFA), and microwave ablation (MWA). Overall survival (OS), disease-free survival (DFS), and recurrence were compared between patients with and without bridging therapy. The prognostic significance of pathological CR was also assessed.

Results: Bridging therapy was administered to 24.2% of patients. There was no statistically significant difference in OS or DFS between patients who received bridging therapy and those who did not. However, a pathological CR was achieved in 27.6% of bridged patients and was significantly associated with improved OS (P = .018) and DFS (P = .05). No recurrence or mortality occurred in patients who achieved CR.

Conclusion: While bridging therapy did not independently affect post-transplant survival, achieving a pathological complete response emerged as a strong prognostic indicator. These findings highlight the clinical importance of treatment response and support the role of CR as a potential predictor of favorable long-term outcomes following LT in HCC patients.

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