Prognostic Hematologic Biomarkers Following Immune Checkpoint Inhibition in Metastatic Uveal Melanoma.

LDH NLR immune checkpoint inhibitors ocular melanoma prognosis uveal melanoma

Journal

Cancers
ISSN: 2072-6694
Titre abrégé: Cancers (Basel)
Pays: Switzerland
ID NLM: 101526829

Informations de publication

Date de publication:
24 Nov 2022
Historique:
received: 04 10 2022
revised: 21 11 2022
accepted: 22 11 2022
entrez: 11 12 2022
pubmed: 12 12 2022
medline: 12 12 2022
Statut: epublish

Résumé

Background: There is no standardized treatment for metastatic uveal melanoma (MUM) but immune checkpoint inhibitors (ICI) are increasingly used. While ICI has transformed the survival of metastatic cutaneous melanoma, MUM patients do not equally benefit. Factors known to affect ICI response include the hematologic markers, lactate dehydrogenase (LDH) and neutrophil:lymphocyte ratio (NLR). We evaluated the prognostic value of LDH and NLR at the start of ICI and on treatment in MUM. Methods: MUM patients were treated between August 2006 and May 2022 with combination ipilimumab/nivolumab or ipilimumab/nivolumab/pembrolizumab single-agent therapy. Univariable (UVA) and multivariable (MVA) analyses were used to assess the prognostic value of predefined baseline factors on progression-free (PFS) and overall survival (OS). Results: In forty-six patients with MUM treated with ICI, elevated baseline and on-treatment LDH was prognostic for OS (start of ICI, HR (95% CI): 3.6 (1.9−7.0), p < 0.01; on-treatment, HR (95% CI): 3.7 (1.6−8.8), p < 0.01) and PFS (start of ICI, (HR (95% CI): 2.8 (1.5−5.4), p < 0.0001); on-treatment LDH (HR (95% CI): 2.2 (1.1−4.3), p < 0.01). On-treatment NLR was prognostic for PFS (HR (95% CI): 1.9 (1.0−3.9), p < 0.01). On-treatment LDH remained an important contributor to survival on MVA (OS: HR (95% CI): 1.001 (1.00−1.002), p < 0.05); PFS: HR (95% CI): 1.001 (1.00−1.002), p < 0.01). Conclusions: This study demonstrates that LDH and NLR could be useful in the prognostication of MUM patients treated with ICI. Additional studies are needed to confirm the importance of these and other prognostic biomarkers.

Identifiants

pubmed: 36497270
pii: cancers14235789
doi: 10.3390/cancers14235789
pmc: PMC9738244
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : Medical Scientist Training program
ID : GM007863
Organisme : University of Michigan Rackham Merit Fellowship
ID : na
Organisme : Lung Precision Oncology Program
ID : VA 150CU000182
Organisme : LUNGevity, Breast Cancer Research Foundation, Melanoma Research Alliance
ID : MRA689853
Organisme : BLRD VA
ID : I01 BX005267
Pays : United States
Organisme : NCI NIH HHS
ID : CA252010
Pays : United States
Organisme : Richard N and Marilyn K Witham professorship
ID : na

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Auteurs

Jessica J Waninger (JJ)

Medical Scientist Training Program, University of Michigan, Ann Arbor, MI 48109, USA.

Leslie A Fecher (LA)

Department of Internal Medicine, Division of Hematology Oncology, Rogel Cancer Center, Ann Arbor, MI 48109, USA.

Christopher Lao (C)

Department of Internal Medicine, Division of Hematology Oncology, Rogel Cancer Center, Ann Arbor, MI 48109, USA.

Sarah Yentz (S)

Department of Internal Medicine, Division of Hematology Oncology, Rogel Cancer Center, Ann Arbor, MI 48109, USA.

Michael D Green (MD)

Department of Radiation Oncology, University of Michigan, Ann Arbor, MI 48109, USA.
Department of Microbiology and Immunology, University of Michigan, Ann Arbor, MI 48109, USA.
Department of Radiation Oncology, Veterans Affairs Ann Arbor Healthcare System, Ann Arbor, MI 48105, USA.

Hakan Demirci (H)

Department of Ophthalmology and Visual Sciences, University of Michigan, Ann Arbor, MI 48105, USA.

Classifications MeSH