Evidence map›Paper›PMID 37187974›Full record

ArticleOncoimmunology2023

Preexisting autoantibodies as predictor of immune related adverse events (irAEs) for advanced solid tumors treated with immune checkpoint inhibitors (ICIs).

A Daban, C Gonnin, L Phan, A Saldmann, C Granier, A Lillo-Lelouet, C Le Beller, J Pouchot, L Weiss, E Tartour and 6 more

Open access · goldAbstract read
In one paragraph

Article in Oncoimmunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 1 pooled it
7.1field-weighted citation impact, top 3% of its field
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

28 citing papers in PubMed, 1 synthesis or guideline pooled it, 31 citations in OpenAlex.

  1. Pooled it
  2. The Immune Checkpoint Inhibitors Journey: From Early Promise to Lasting Impact.Journal of immunotherapy and precision oncology · 2026
    Review
  3. Article
  4. Review
  5. Humoral contributions to checkpoint blockade therapy.Journal for immunotherapy of cancer · 2026
    Article
  6. Review
  7. Observational
  8. Review
  9. Article
  10. Article
  11. Observational
  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. [Endocrine side effects of tumor treatment].Innere Medizin (Heidelberg, Germany) · 2024
    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

16 authors at 2 institutions in 1 country.

A DabanDepartment of Medical Oncology, Hôpital Européen Georges Pompidou, Institut du Cancer Paris CARPEM, AP-HP.Centre - Université Paris Cité, Paris, France.
C GonninDepartment of Immunology, Hôpital Européen Georges Pompidou, AP-HP.Centre - Université Paris Cité, Paris, France.
L PhanARTIC - Association pour la Recherche de Thérapeutiques Innovantes en Cancérologie; Hǒpital Européen Georges Pompidou, AP-HP. Centre - Université Paris Cité, Paris, France.
A SaldmannDepartment of Immunology, Hôpital Européen Georges Pompidou, AP-HP.Centre - Université Paris Cité, Paris, France.
C GranierDepartment of Immunology, Hôpital Européen Georges Pompidou, AP-HP.Centre - Université Paris Cité, Paris, France.
A Lillo-LelouetDepartment of Pharmacovigilance, Hôpital Européen Georges Pompidou, AP-HP.Centre - Université Paris Cité, Paris, France.
C Le BellerDepartment of Pharmacovigilance, Hôpital Européen Georges Pompidou, AP-HP.Centre - Université Paris Cité, Paris, France.
J PouchotDepartment of Internal Medicine, Hôpital Européen Georges Pompidou, AP-HP.Centre - Université Paris Cité, Paris, France.
L WeissDepartment of Clinical Immunology, Hôpital Hôtel-Dieu, AP-HP.Centre - Université Paris Cité, Paris, France.
E TartourDepartment of Immunology, Hôpital Européen Georges Pompidou, AP-HP.Centre - Université Paris Cité, Paris, France.
E FabreINSERM U970, PARCC, Université Paris-Cité, Paris, France.
J MedioniDepartment of Medical Oncology, Hôpital Européen Georges Pompidou, Institut du Cancer Paris CARPEM, AP-HP.Centre - Université Paris Cité, Paris, France.
S OudardDepartment of Medical Oncology, Hôpital Européen Georges Pompidou, Institut du Cancer Paris CARPEM, AP-HP.Centre - Université Paris Cité, Paris, France.
Y A VanoDepartment of Medical Oncology, Hôpital Européen Georges Pompidou, Institut du Cancer Paris CARPEM, AP-HP.Centre - Université Paris Cité, Paris, France.
M A Dragon-DureyDepartment of Immunology, Hôpital Européen Georges Pompidou, AP-HP.Centre - Université Paris Cité, Paris, France.
A SimonaggioDepartment of Medical Oncology, Hôpital Européen Georges Pompidou, Institut du Cancer Paris CARPEM, AP-HP.Centre - Université Paris Cité, Paris, France.
Université Paris Cité · FRInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionImmune checkpoint inhibitors (ICIs) are now standard of care in many cancers. They can generate immune-related adverse events (irAEs), but no biomarkers are available to identify patients who are more likely to develop irAEs. We assess the association between pre-existing autoantibodies and occurrence of irAEs. PATIENTS AND

methodsWe prospectively collected data from consecutive patients receiving ICIs for advanced cancers, in a single center between May 2015 and July 2021. Autoantibodies testing was performed before ICIs initiation including AntiNeutrophil Cytoplasmic Antibodies, Antinuclear Antibodies, Rheumatoid Factor anti-Thyroid Peroxidase and anti-Thyroglobulin. We analyzed the associations of pre-existing autoantibodies with onset, severity, time to irAEs and with survival outcomes.

resultsOf the 221 patients included, most had renal cell carcinoma (n = 99; 45%) or lung carcinoma (n = 90; 41%). Grade ≥2 irAEs were more frequent among patients with pre-existing autoantibodies: 64 (50%) vs. 20 (22%) patients (Odds-Ratio= 3.5 [95% CI=1.8-6.8]; p < 0.001) in the positive vs negative group, respectively. irAEs occurred earlier in the positive group with a median time interval between ICI initiation and irAE of 13 weeks (IQR = 8.8-21.6) vs. 28.5 weeks (IQR=10.6-55.1) in the negative group (p = 0.01). Twelve patients (9.4%) experienced multiple (≥2) irAEs in the positive group vs. 2 (2%) in the negative group (OR = 4.5 [95% CI: 0.98-36], p = 0.04). After a median follow-up of 25 months, median PFS and OS were significantly longer among patients experiencing irAE (p = 0.00034 and p = 0.016, respectively).

conclusionThe presence of pre-existing autoantibodies is significantly associated with the occurrence of grade ≥2 irAEs, with earlier and multiple irAEs in patients treated with ICIs.

Indexed as

Antineoplastic Agents, ImmunologicalKidney NeoplasmsLung NeoplasmsAutoantibodiesHumansImmune Checkpoint InhibitorsRetrospective StudiesAntineoplastic Agents, ImmunologicalAutoantibodiesImmune Checkpoint InhibitorsImmune checkpoint inhibitorsimmune-related adverse eventspre-existing antibodies

Identifiers

PMID37187974
PMCPMC10177742
OpenAlexW4376643165

What OpenQuestion holds

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LicenceCC BY-NC
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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.