Evidence map›Paper›PMID 38945553›Full record

ArticleJournal for immunotherapy of cancer2024

Autoantibody-positivity before and seroconversion during treatment with anti-PD-1 is associated with immune-related adverse events in patients with melanoma.

Jessica S W Borgers, Tineke J van Wesemael, Kyra A Gelderman, Theo Rispens, Els M E Verdegaal, Dirk J A R Moes, Catharina M Korse, Ellen Kapiteijn, Marij J P Welters, Sjoerd H van der Burg and 4 more

Abstract readMulticenter Study
In one paragraph

Article in Journal for immunotherapy of cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
–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

12 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Humoral contributions to checkpoint blockade therapy.Journal for immunotherapy of cancer · 2026
    Article
  4. Strategies to target PD-1/PD-L1 in the tumor microenvironment.Cellular oncology (Dordrecht, Netherlands) · 2026
    Review
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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

14 authors.

Jessica S W BorgersMedical Oncology, Netherlands Cancer Institute, Amsterdam, Noord-Holland, Netherlands.ORCID http://orcid.org/0000-0002-6478-7821
Tineke J van WesemaelRheumatology, Leiden University Medical Center, Leiden, Zuid-Holland, Netherlands.
Kyra A GeldermanSanquin Diagnostic Services, Amsterdam, Noord-Holland, Netherlands.
Theo RispensDepartment of Immunopathology, Sanquin Research and Landsteiner Laboratory, Amsterdam, Noord-Holland, UK.
Els M E VerdegaalMedical Oncology, Oncode Institute, Leiden University Medical Center, Leiden, Zuid-Holland, Netherlands.ORCID http://orcid.org/0000-0002-4449-8707
Dirk J A R MoesClinical Pharmacy and Toxicology, Leiden University Medical Center, Leiden, Zuid-Holland, Netherlands.
Catharina M KorseLaboratory Medicine, Netherlands Cancer Institute, Amsterdam, Netherlands.
Ellen KapiteijnDepartment of Medical Oncology, Leiden University Medical Center, Leiden, Zuid-Holland, Netherlands.ORCID http://orcid.org/0000-0002-4814-6426
Marij J P WeltersMedical Oncology, Oncode Institute, Leiden University Medical Center, Leiden, Netherlands.
Sjoerd H van der BurgMedical Oncology, Oncode Institute, Leiden University Medical Center, Leiden, Netherlands.ORCID http://orcid.org/0000-0002-6556-0354
Winan J van HoudtSurgical Oncology, Netherlands Cancer Institute, Amsterdam, Noord-Holland, Netherlands.
Johannes V van ThienenMedical Oncology, Netherlands Cancer Institute, Amsterdam, Noord-Holland, Netherlands.
John B A G HaanenMedical Oncology, Netherlands Cancer Institute, Amsterdam, Noord-Holland, Netherlands j.haanen@nki.nl.ORCID http://orcid.org/0000-0001-5884-7704
Diane van der WoudeRheumatology, Leiden University Medical Center, Leiden, Zuid-Holland, Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionTreatment with the immune checkpoint inhibitor anti-programmed cell death protein-1 (PD-1) often causes immune-related adverse events (irAEs). Since irAEs resemble autoimmune diseases, autoantibodies might play a role and could potentially be used to identify patients at risk. Therefore, we investigated the association between autoantibody-positivity and toxicity as well as clinical response in patients with melanoma treated with anti-PD-1. MATERIALS AND

methodsThis two-center, retrospective study included 143 patients with melanoma treated with anti-PD-1. Toxicities grade ≥2 and recurrences/responses were captured until 6 months after treatment initiation. Autoantibody measurements were performed at baseline and 3 months after treatment initiation, including IgM-rheumatoid factor (RF), antinuclear antibodies (ANA), extractable nuclear antigen, anti-cyclic citrullinated peptide antibodies (anti-CCP2) and anti-thyroid antibodies.

results169 irAEs were experienced by 86/143 patients (137 grades 1-2, 32 grades 3-4), the most common being thyroiditis (n=25), dermatitis (n=24), and sicca problems (n=19). Patients with autoantibodies at baseline experienced more irAEs (p=0.001), predominantly associated with anti-thyroid antibodies and thyroid dysfunction. No association was observed between any irAE and anti-CCP2, RF or ANA. In women, baseline and on-treatment anti-thyroid antibody-positivity as well as seroconversion during treatment was associated with thyroid dysfunction. In men, this association was only observed on-treatment. The presence of autoantibodies was not associated with melanoma recurrence (p=0.776) or response (p=0.597).

conclusionThe presence of autoantibodies prior to anti-PD-1 therapy is associated with irAEs in patients with melanoma. Both baseline positivity and seroconversion of anti-thyroid antibodies were strongly associated with thyroid dysfunction. This association was stronger in women, with all women who were baseline positive developing thyroid dysfunction.

Indexed as

AutoantibodiesImmune Checkpoint InhibitorsMelanomaSeroconversionAdultAgedAged, 80 and overFemaleHumansMaleMiddle AgedProgrammed Cell Death 1 ReceptorRetrospective StudiesAutoantibodiesImmune Checkpoint InhibitorsProgrammed Cell Death 1 ReceptorImmune Checkpoint InhibitorImmune related adverse event - irAESkin Cancer

Identifiers

PMID38945553
PMCPMC11216046

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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.