Please use this identifier to cite or link to this item: http://ahro.austin.org.au/austinjspui/handle/1/23930
Title: A pilot study of intrahepatic yttrium-90 microsphere radioembolization in combination with intravenous cisplatin for uveal melanoma liver-only metastases.
Authors: Arulananda, Surein;Parakh, Sagun;Palmer, Jodie;Goodwin, Mark D;Andrews, Miles C;Cebon, Jonathan S
Affiliation: Department of Medicine, University of Melbourne, Parkville, Victoria, Australia
Cancer Immuno-Biology Laboratory, Olivia Newton-John Cancer Research Institute, Heidelberg, Victoria, Australia
School of Cancer Medicine, La Trobe University, Bundoora, Victoria, Australia
Department of Radiology, Austin Health, Heidelberg, Victoria, Australia
Department of Medical Oncology, Austin Health, Heidelberg, Victoria, Australia
Issue Date: Aug-2019
EDate: 2019-05-14
Citation: Cancer reports (Hoboken, N.J.) 2019; 2(4): e1183
Abstract: Metastatic uveal melanoma is a highly aggressive disease with no standard of care treatment option. A large proportion of patients have liver-only metastatic disease which raises the question if liver-directed therapy can be efficacious in this subpopulation. The study aims to evaluate the safety and efficacy of radiosensitizing chemotherapy in combination with yttrium-90 microspheres in patients with uveal melanoma with liver-only metastases. This single arm, open labeled, non-randomized study enrolled 10 patients with liver-only metastatic uveal melanoma between November 2012 and January 2018. Eligible patients received intrahepatic yttrium-90 microspheres followed by intravenous cisplatin (20 mg/m2) for 5 days. Ten patients were enrolled, but nine patients received treatment who were included in the final analysis with a median follow-up of 30 months (range 7 to 44). Five (50%) were female, five (50%) had an elevated lactate dehydrogenase (LDH), and one (10%) had prior anti-PD-1 therapy. The combination was well tolerated with no greater than or equal to grade 3 toxicity observed. The liver objective response rate (ORR) was 33% (3/9), the median progression-free survival (PFS) in the liver was 3 months (95% CI, 3-NA), and the extrahepatic PFS was 3 months (95% CI, 3-NA). Seventy-eight percent (7/9) received an immune checkpoint inhibitor on disease progression, with no responses seen. The median overall survival (OS) was 10 months (95% CI, 7-NA). The combination of cisplatin with yttrium-90 microspheres was well tolerated; however, it was associated with intrahepatic disease control of relatively short duration. No responses were seen in patients treated with immune checkpoint inhibitors post radioembolization.
URI: http://ahro.austin.org.au/austinjspui/handle/1/23930
DOI: 10.1002/cnr2.1183
ORCID: 0000-0002-5636-6381
0000-0003-3891-2489
0000-0003-1231-8641
0000-0002-3898-950X
PubMed URL: 32721131
Type: Case Reports
Subjects: anti‐PD‐1 therapy
chemotherapy
uveal melanoma
yttrium‐90 microspheres
Appears in Collections:Journal articles

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