经皮肝灌注 (PHP) 作为转移性葡萄膜黑色素瘤的一线或二线疗法后的肝脏和总体无进展生存期。

IF 3.4 2区 医学 Q2 ONCOLOGY
Annals of Surgical Oncology Pub Date : 2024-12-01 Epub Date: 2024-08-22 DOI:10.1245/s10434-024-16039-5
Helana Ghali, Michelle M Dugan, Shaliz Aflatooni, Aleena Boby, Danielle K DePalo, José Laborde, Junsung Choi, Altan F Ahmed, Jonathan S Zager
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引用次数: 0

摘要

背景:葡萄膜黑色素瘤常转移至肝脏,预后较差。通过经皮肝灌注(PHP)的美法仑/肝脏给药系统(HDS)是一种通过受影响肝脏循环高剂量化疗的微创方法。本研究评估了美法仑/HDS作为一线或二线治疗的使用情况,以指导治疗排序:回顾性研究纳入了2008年至2023年期间通过PHP接受美法仑/HDS治疗的肝转移性葡萄膜黑色素瘤患者:共发现30例患者,53.3%为女性,中位年龄为63.5岁(37-78岁)。中位随访时间为 14.5 个月。一线疗法包括美法仑/HDS(17 例)、肝脏导向疗法(7 例)和免疫疗法(6 例)。二线疗法包括美法仑/HDS(6例)、免疫疗法(5例)和肝脏导向疗法(3例)。一线美法仑/HDS、免疫疗法和肝脏导向疗法的中位肝脏无进展生存期(hPFS)分别为17.6/8.8/9.2个月(P = 0.002)。二线美罗啡/HDS、免疫疗法和肝脏导向疗法的中位生存期分别为14.7/7.5个月(P<0.001)。一线美法仑/HDS、免疫疗法和肝脏导向疗法的中位总生存时间分别为15.4/8.8/9.2个月(P = 0.04)。二线美法仑/HDS、免疫疗法和肝脏导向疗法的中位总生存期分别为22.2/14.7/7.5个月(P = 0.001):通过PHP治疗转移至肝脏的葡萄膜黑色素瘤的美法仑/HDS,与免疫疗法或肝脏导向疗法相比,作为一线疗法可显著改善hPFS和总PFS。与二线免疫疗法或肝脏导向疗法相比,PHP 作为二线疗法时的 hPFS 和 PFS 继续得到改善。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hepatic and Overall Progression-Free Survival After Percutaneous Hepatic Perfusion (PHP) as First-Line or Second-Line Therapy for Metastatic Uveal Melanoma.

Background: Uveal melanoma often metastasizes to the liver, portending a poor prognosis. Melphalan/hepatic delivery system (HDS) via percutaneous hepatic perfusion (PHP) is a minimally invasive means of circulating high-dose chemotherapy through the affected liver. This study evaluated melphalan/HDS use as either first-line or second-line treatment to guide treatment sequencing.

Patients and methods: A retrospective review included patients with hepatic-dominant metastatic uveal melanoma who underwent melphalan/HDS treatment via PHP from 2008 to 2023.

Results: A total of 30 patients were identified; 53.3% female, with a median age of 63.5 years (37-78 years). Median follow-up time was 14.5 months. First-line therapies included melphalan/HDS (n = 17), liver-directed (n = 7), and immunotherapy (n = 6). Second-line therapies included melphalan/HDS (n = 6), immunotherapy (n = 5), and liver-directed (n = 3). Median hepatic progression-free survival (hPFS) for first-line melphalan/HDS, immunotherapy, and liver-directed therapy was 17.6/8.8/9.2 months, respectively (P = 0.002). Median hPFS for second-line melphalan/HDS, immunotherapy, and liver-directed therapy was not reached/14.7/7.5 months, respectively (P < 0.001). Median overall PFS for first-line melphalan/HDS, immunotherapy, and liver-directed therapy was 15.4/8.8/9.2 months, respectively (P = 0.04). Median overall PFS for second-line melphalan/HDS, immunotherapy, and liver-directed therapy was 22.2/14.7/7.5 months, respectively (P = 0.001).

Conclusions: Melphalan/HDS via PHP for metastatic uveal melanoma to the liver was found to have significantly improved hPFS and overall PFS when used as first-line therapy compared with immunotherapy or liver-directed therapy. PHP continued to demonstrate improved hPFS and PFS when used as second-line therapy compared with second-line immunotherapy or liver-directed therapy.

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来源期刊
CiteScore
5.90
自引率
10.80%
发文量
1698
审稿时长
2.8 months
期刊介绍: The Annals of Surgical Oncology is the official journal of The Society of Surgical Oncology and is published for the Society by Springer. The Annals publishes original and educational manuscripts about oncology for surgeons from all specialities in academic and community settings.
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