Percutaneous hepatic perfusion with melphalan in uveal melanoma: A safe and effective treatment modality in an orphan disease. Issue 6 (28th December 2017)

• Record Type: Journal Article
• Authors: 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
• Is Part Of: Journal of surgical oncology. Volume 117:Issue 6(2018)
• Page Start: 1170
• Page End: 1178
• Publication Date: 2017-12-28
• Subjects: chemosaturation -- intrahepatic percutaneous haemoperfusion -- liver metastasis -- melphalan -- unresectable liver tumor -- uveal melanoma; Cancer -- Surgery -- Periodicals; Neoplasms -- Periodicals; 616
• DOI: 10.1002/jso.24956
• Languages: English
• ISSNs: 0022-4790

Abstract

Abstract : Background: 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. Methods: 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. Results: 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). Conclusions: M‐PHP results in durable intrahepatic disease control and can form the basis for an integrated multimodality treatment approach in appropriately selected UM patients.