Pilot trial of arginine deprivation plus nivolumab and ipilimumab in patients with metastatic uveal melanoma Journal Article


Authors: Kraehenbuehl, L.; Holland, A.; Armstrong, E.; O'Shea, S.; Mangarin, L.; Chekalil, S.; Johnston, A.; Bomalaski, J. S.; Erinjeri, J. P.; Barker, C. A.; Francis, J. H.; Wolchok, J. D.; Merghoub, T.; Shoushtari, A. N.
Article Title: Pilot trial of arginine deprivation plus nivolumab and ipilimumab in patients with metastatic uveal melanoma
Abstract: Simple Summary: Uveal melanoma is a rare subtype of malignant melanoma. It is known to rapidly metastasize, with the liver being the most frequently affected organ. Due to differences from melanoma arising in the skin, such as a lower number of mutations, it responds poorly to immune checkpoint blockade, a treatment approach reinvigorating the patient's immune system to eliminate the cancer. We here investigated the safety and tolerability of a new combination treatment consisting of two established immunotherapy medications (ipilimumab and nivolumab) with the addition of an experimental arginine depleting medication, pegylated arginine deiminase (ADI-PEG 20), which is thought to make uveal melanoma more amenable to immunotherapy. This novel treatment approach was found to be safe and well-tolerated but did not improve the clinical outcome beyond the expected limited efficacy of approved immunotherapy alone. Metastatic uveal melanoma (UM) remains challenging to treat, with objective response rates to immune checkpoint blockade (ICB) being much lower than in primary cutaneous melanoma (CM). Besides a lower mutational burden, the overall immune-excluded tumor microenvironment of UM might contribute to the poor response rate. We therefore aimed at targeting deficiency in argininosuccinate synthase 1, which is a key metabolic feature of UM. This study aims at investigating the safety and tolerability of a triple combination consisting of ipilimumab and nivolumab immunotherapy and the metabolic therapy, ADI-PEG 20. Nine patients were enrolled in this pilot study. The combination therapy was safe and tolerable with an absence of immune-related adverse events (irAE) of special interest, but with four of nine patients experiencing a CTCAE grade 3 AE. No objective responses were observed. All except one patient developed anti-drug antibodies (ADA) within a month of the treatment initiation and therefore did not maintain arginine depletion. Further, an IFNg-dependent inflammatory signature was observed in metastatic lesions in patients pre-treated with ICB compared with patients with no pretreatment. Multiplex immunohistochemistry demonstrated variable presence of tumor infiltrating CD8 lymphocytes and PD-L1 expression at the baseline in metastases.
Keywords: immunohistochemistry; membrane proteins; immunotherapy; t-lymphocytes, regulatory; patient safety; drug tolerance; enzymes; pilot studies; treatment outcomes; cancer patients; neoplasm metastasis -- drug therapy; melanoma -- drug therapy; antineoplastic agents, combined; uveal neoplasms -- drug therapy; ipilimumab -- therapeutic use; human; nivolumab -- therapeutic use; immune checkpoint inhibitors -- therapeutic use; programmed cell death ligand 1; arginine -- blood
Journal Title: Cancers
Volume: 14
Issue: 11
ISSN: 2072-6694
Publisher: MDPI  
Date Published: 2022-06-01
Start Page: 2638
Language: English
DOI: 10.3390/cancers14112638
PROVIDER: EBSCOhost
PROVIDER: cinahl
PMCID: PMC9179243
PUBMED: 35681616
DOI/URL:
Notes: Accession Number: 157372318 -- Entry Date: 20220629 -- Revision Date: 20220629 -- Publication Type: Article; pictorial; research; tables/charts -- Journal Subset: Biomedical; Continental Europe; Europe -- NLM UID: 101526829. -- Source: Cinahl
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MSK Authors
  1. Jedd D Wolchok
    905 Wolchok
  2. Taha Merghoub
    364 Merghoub
  3. Jasmine Helen Francis
    256 Francis
  4. Christopher Barker
    218 Barker
  5. Joseph Patrick Erinjeri
    200 Erinjeri
  6. Aliya Rose Ming Holland
    18 Holland
  7. Sirinya O'Shea
    1 O'Shea