Evidence map›Paper›PMID 42247661›Full record

ArticleJournal of veterinary internal medicine2026

Efficacy and safety evaluation of gilvetmab in dogs with melanoma and mast cell tumor.

Esther Chon, Mohamad Morsey, Terry Katz, Kazumi Yamada, Dennis Bailey, Philip J Bergman, Holly Burr, Craig A Clifford, Heather Heeb, Christina Manley and 5 more

Abstract readClinical Trial, VeterinaryMulticenter Study
In one paragraph

Article in Journal of veterinary internal medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors.

Esther ChonMerck Animal Health, Rahway, NJ, United States.
Mohamad MorseyMerck Animal Health, Rahway, NJ, United States.
Terry KatzMerck Animal Health, Rahway, NJ, United States.
Kazumi YamadaMerck Animal Health, Rahway, NJ, United States.
Dennis BaileyOradell Animal Hospital, Paramus, NJ, United States.
Philip J BergmanVCA Katonah Bedford Veterinary Center, Bedford Hills, NY, United States.
Holly BurrLas Vegas Veterinary Specialty Center, Las Vegas, NV, United States.
Craig A CliffordBluePearl Pet Hospital Malvern, Malvern, PA, United States.
Heather HeebBluePearl Veterinary Specialty Hospital in Overland Park, Overland Park, KS, United States.
Christina ManleyThe Oncology Service at the LifeCentre, Leesburg, VA, United States.
Brenda PhillipsVeterinary Specialty Hospital - Sorrento Valley, San Diego, CA, United States.
Gerald PostMedVet Norwalk, Norwalk, CT, United States.
David M VailDepartment of Medical Sciences, School of Veterinary Medicine, Madison, WI, United States.
Anthony RuskACI Biosciences, LLC, Chevy Chase, MD, United States.
Matthew L StockMerck Animal Health, Rahway, NJ, United States.

Funding

Merck Animal Health
6 · The paper itself

Abstract

backgroundImmune checkpoint inhibitors (ICIs) have transformed oncology in human medicine, providing clinical benefit in a broad spectrum of cancers. Widely available ICIs for dogs are lacking. HYPOTHESIS/

objectivesEvaluate efficacy and safety of gilvetmab, a caninized anti-PD-1 monoclonal antibody. ANIMALS: Fifty-one client-owned dogs were evaluated, 25 with stages II-III melanoma and 26 with stages I-III mast cell tumor (MCT). Fifteen dogs with stages III-V lymphoma were also evaluated.

methodsMulti-institutional, open-label study. Enrolled dogs were treated with gilvetmab IV at 6 mg/kg q28d or 10 mg/kg q14d; 8 dogs receiving the lower dosage underwent dose escalation with their owners' consent. Safety was evaluated by physical examinations, laboratory testing, and clinical observations made by veterinarians or the dogs' owners. Efficacy was assessed by objective response rate (ORR) and time to progression (TTP) using cRECIST v1.0 and lymphoma response criteria.

resultsFor melanoma, the ORR was 20% (95% confidence interval [CI], 7%-41%) and median TTP was 56 days. For MCT, the ORR was 46% (95% CI, 27%-67%) and median TTP was not reached. No objective responses were observed in dogs with lymphoma. Serious adverse events of anaphylaxis, hypotension, or tumor hemorrhage occurred in 3 dogs (3/51, 5.9%). Tumor enlargement before regression, consistent with possible pseudoprogression, was observed in 2 dogs with melanoma. CONCLUSIONS AND CLINICAL IMPORTANCE: Gilvetmab has a reasonable expectation of efficacy and an acceptable preliminary safety profile in dogs with MCT stages I-III and melanoma stages II and III.

Indexed as

Dog DiseasesImmune Checkpoint InhibitorsMastocytomaMelanomaAnimalsDogsFemaleMaleSkin NeoplasmsTreatment OutcomeImmune Checkpoint Inhibitorscancercanineimmune checkpoint inhibitorimmunotherapymonoclonal antibodyPD-1Programmed cell death 1 receptor

Identifiers

PMID42247661
PMCPMC13240851

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.