Evidence map›Paper›PMID 39964344›Full record

ArticleACR open rheumatology2025

Chronicity of Immune Checkpoint Inhibitor-Associated Inflammatory Arthritis After Immunotherapy Discontinuation: Results From the Canadian Research Group of Rheumatology in Immuno-Oncology Database.

Alexandra Ladouceur, Shahin Jamal, Alexandra Saltman, Megan Himmel, Marie Hudson, Janet Pope, Sabrina Hoa, Janet Roberts, Inés Colmegna, Lourdes Gonzalez Arreola and 8 more

Abstract read
In one paragraph

Article in ACR open rheumatology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. The Immune Checkpoint Inhibitors Journey: From Early Promise to Lasting Impact.Journal of immunotherapy and precision oncology · 2026
    Review
  2. Article
  3. Observational
  4. Review
  5. Article
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

18 authors.

Alexandra LadouceurMcGill University, Montreal, Quebec, Canada.ORCID https://orcid.org/0009-0009-3755-4860
Shahin JamalUniversity of British Columbia, Vancouver, British Columbia, Canada.ORCID https://orcid.org/0000-0001-5870-3567
Alexandra SaltmanUniversity of Toronto, Toronto, Ontario, Canada.
Megan HimmelUniversity of Toronto, Toronto, Ontario, Canada.
Marie HudsonMcGill University, Montreal, Quebec, Canada.
Janet PopeUniversity of Western Ontario, London, Ontario, Canada.ORCID https://orcid.org/0000-0003-1479-5302
Sabrina HoaUniversité de Montréal, Montreal, Quebec, Canada.ORCID https://orcid.org/0000-0002-9466-5729
Janet RobertsDalhousie University, Halifax, Nova Scotia, Canada.
Inés ColmegnaMcGill University, Montreal, Quebec, Canada.
Lourdes Gonzalez ArreolaArthritis Research Canada, Vancouver, British Columbia, Canada.
Tatiana NevskayaUniversity of Western Ontario, London, Ontario, Canada.
Ammana KarmaliArthritis Research Canada, Vancouver, British Columbia, Canada.
David MoonUniversity of Alberta, Edmonton, Alberta, Canada.
Emma SchmidtUniversity of British Columbia, Vancouver, British Columbia, Canada.
Nader TobanUniversité de Montréal, Montreal, Quebec, Canada.
Lindsay ChoDalhousie University, Halifax, Nova Scotia, Canada.
Thomas BarnetcheCentre Hospitalier Universitaire de Bordeaux, Bordeaux, France.
Carrie YeUniversity of Alberta, Edmonton, Alberta, Canada.ORCID https://orcid.org/0000-0002-9858-5398

Funding

CIHR CIHR PS 192087
6 · The paper itself

Abstract

objectiveImmune checkpoint inhibitors (ICIs) improve overall survival (OS) and progression-free survival (PFS) in many types of malignancies but can result in off-target immune-related adverse events including inflammatory arthritis (ICI-associated inflammatory arthritis [ICI-IA]), which can persist even after ICI cessation. We aimed to examine the proportion of patients with ICI-IA who develop chronic ICI-IA and describe characteristics and outcomes associated with chronic ICI-IA.

methodsWe identified patients from the Canadian Research Group of Rheumatology in Immuno-Oncology retrospective cohort who developed de novo ICI-IA with at least three months of follow-up after ICI cessation. Chronic ICI-IA was defined as symptoms or ongoing immunosuppression lasting beyond three months after ICI discontinuation. Acute ICI-IA was defined as resolution of ICI-IA symptoms and discontinuation of immunosuppression within three months of ICI discontinuation. OS and PFS were assessed with Kaplan-Meier curves. Landmark multivariable Cox proportional hazard models for OS and PFS were conducted.

resultsThe study cohort included 119 patients. A total of 15 patients (13%) had acute ICI-IA, whereas 104 (87%) had chronic ICI-IA. Patients with chronic ICI-IA were more likely to be White and to have polyarthritis at presentation. After adjusting for age, sex, tumor type, stage of cancer, ICI-IA treatment, and time from ICI initiation to ICI-IA onset, patients with chronic ICI-IA had greater PFS from ICI initiation (adjusted hazard ratio 0.27, 95% confidence interval 0.08-0.98; P = 0.046). Adjusted hazard ratio for OS was similar between those with acute versus chronic ICI-IA.

conclusionICI-IA frequently persists after ICI discontinuation. Chronic ICI-IA is associated with improved PFS, but not OS, as compared to acute ICI-IA.

Identifiers

PMID39964344
PMCPMC11834585

What OpenQuestion holds

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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.