Karydis Ioannis, Gangi Alexandra, Wheater Matthew J, Choi Junsung, Wilson Iain, Thomas Kerry, Pearce Neil, Takhar Arjun, Gupta Sanjay, Hardman Danielle, Sileno Sean, Stedman Brian, Zager Jonathan S, Ottensmeier Christian
Cancer Sciences Academic Unit, University of Southampton, Southampton, United Kingdom.
University Hospital Southampton, Southampton, United Kingdom.
J Surg Oncol. 2018 May;117(6):1170-1178. doi: 10.1002/jso.24956. Epub 2017 Dec 28.
Metastatic uveal melanoma (UM) carries a poor prognosis; liver is the most frequent and often solitary site of recurrence. Available systemic treatments have not improved outcomes. Melphalan percutaneous hepatic perfusion (M-PHP) allows selective intrahepatic delivery of high dose cytotoxic chemotherapy.
Retrospective analysis of outcomes data of UM patients receiving M-PHP at two institutions was performed. Tumor response and toxicity were evaluated using RECIST 1.1 and Common Terminology Criteria for Adverse Events (CTCAE) v4.03, respectively.
A total of 51 patients received 134 M-PHP procedures (median of 2 M-PHPs). 25 (49%) achieved a partial (N = 22, 43.1%) or complete hepatic response (N = 3, 5.9%). In 17 (33.3%) additional patients, the disease stabilized for at least 3 months, for a hepatic disease control rate of 82.4%. After median follow-up of 367 days, median overall progression free (PFS) and hepatic progression free survival (hPFS) was 8.1 and 9.1 months, respectively and median overall survival was 15.3 months. There were no treatment related fatalities. Non-hematologic grade 3-4 events were seen in 19 (37.5%) patients and were mainly coagulopathic (N = 8) and cardiovascular (N = 9).
M-PHP results in durable intrahepatic disease control and can form the basis for an integrated multimodality treatment approach in appropriately selected UM patients.
转移性葡萄膜黑色素瘤(UM)预后较差;肝脏是最常见且往往是唯一的复发部位。现有的全身治疗方法并未改善治疗效果。美法仑经皮肝灌注(M-PHP)可实现高剂量细胞毒性化疗药物的选择性肝内递送。
对在两家机构接受M-PHP治疗的UM患者的结局数据进行回顾性分析。分别使用RECIST 1.1和不良事件通用术语标准(CTCAE)v4.03评估肿瘤反应和毒性。
共有51例患者接受了134次M-PHP治疗(中位2次M-PHP)。25例(49%)患者获得部分缓解(N = 22,43.1%)或完全肝脏缓解(N = 3,5.9%)。另有17例(33.3%)患者疾病稳定至少3个月,肝脏疾病控制率为82.4%。中位随访367天后,中位总无进展生存期(PFS)和肝脏无进展生存期(hPFS)分别为8.1个月和9.1个月,中位总生存期为15.3个月。无治疗相关死亡病例。19例(37.5%)患者出现非血液学3-4级事件,主要为凝血功能障碍(N = 8)和心血管事件(N = 9)。
M-PHP可实现持久的肝内疾病控制,并可为适当选择的UM患者的综合多模式治疗方法奠定基础。