Evidence map›Paper›PMID 36270747›Full record

Observational studyRMD open2022

Use of a bDMARD or tsDMARD for the management of inflammatory arthritis under checkpoint inhibitors: an observational study.

Fanny De La Fuente, Rakiba Belkhir, Julien Henry, Chi Duc Nguyen, Thao Pham, Vincent Germain, Pierre Edouard Gavand, Céline Labadie, Claire Briere, Ambre Lauret and 9 more

Open access · goldAbstract readObservational Study
In one paragraph

Observational study in RMD open, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 2 pooled it
2.1field-weighted citation impact, top 11% 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

8 citing papers in PubMed, 2 syntheses or guidelines pooled it, 20 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. The Immune Checkpoint Inhibitors Journey: From Early Promise to Lasting Impact.Journal of immunotherapy and precision oncology · 2026
    Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. 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

19 authors at 7 institutions in 1 country.

Fanny De La FuenteDepartment of Rheumatology, Centre Hospitalier Universitaire de Bordeaux Groupe Hospitalier Pellegrin, Bordeaux, France.
Rakiba BelkhirDepartment of Rheumatology, Hôpital Bicetre, Assistance Publique-Hôpitaux de Paris, FHU CARE, Le Kremlin-Bicetre, France.
Julien HenryDepartment of Rheumatology, Hôpital Bicetre, Assistance Publique-Hôpitaux de Paris, FHU CARE, Le Kremlin-Bicetre, France.
Chi Duc NguyenDepartment of Rheumatology, Centre Hospitalier de Bethune, Bethune, France.
Thao PhamDepartment of Rheumatology, Sainte-Marguerite Hospital, Assistance Publique - Hôpitaux de Marseille, Marseille, France.ORCID 0000-0002-5978-0983
Vincent GermainDepartment of Rheumatology, Centre Hospitalier de Pau, Pau, France.
Pierre Edouard GavandDepartment of Internal Medicine, Clinique Rhena, Strasbourg, France.
Céline LabadieDepartment of Rheumatology, Centre Hospitalier Universitaire de Bordeaux Groupe Hospitalier Pellegrin, Bordeaux, France.
Claire BriereDepartment of Internal Medicine, Centre Hospitalier Intercommunal de Creteil, Creteil, France.
Ambre LauretDepartment of Internal Medicine, Centre Hospitalier Intercommunal de Creteil, Creteil, France.
Thierry CardonDepartment of Rheumatology, Lille University Hospital Center, Lille, France.
Gael MouterdeDepartement of Rheumatology, Lapeyronie Hospital, Montpellier, France.
Isabelle BonnetDepartment of Rheumatology, Hôpital Bicetre, Assistance Publique-Hôpitaux de Paris, FHU CARE, Le Kremlin-Bicetre, France.
Léa RouxelDepartment of Rheumatology, Arcachon Hospital, La Teste de Buch, France.
Marie-Elise TruchetetDepartment of Rheumatology, Centre Hospitalier Universitaire de Bordeaux Groupe Hospitalier Pellegrin, Bordeaux, France.ORCID 0000-0001-8045-0180
Thierry SchaeverbekeDepartment of Rheumatology, Centre Hospitalier Universitaire de Bordeaux Groupe Hospitalier Pellegrin, Bordeaux, France.
Christophe RichezDepartment of Rheumatology, Centre Hospitalier Universitaire de Bordeaux Groupe Hospitalier Pellegrin, Bordeaux, France.ORCID 0000-0002-3029-8739
Marie KostineDepartment of Rheumatology, Centre Hospitalier Universitaire de Bordeaux Groupe Hospitalier Pellegrin, Bordeaux, France marie.kostine@chu-bordeaux.fr.ORCID 0000-0002-6729-6200
Club Rhumatismes and Inflammation (CRI)
Centre Hospitalier Universitaire de Bordeaux · FRInserm · FRHôpital Intercommunal de Créteil · FRAssistance Publique Hôpitaux de Marseille · FRCentre Hospitalier de Béthune · FRCentre Hospitalier De Pau · FRHôpital Lapeyronie · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThere is limited experience regarding the use of biological disease-modifying antirheumatic drug (bDMARD) and JAK inhibitor (JAKi) for the management of immune checkpoint inhibitors (ICI)-induced inflammatory arthritis. We aimed to assess their efficacy and safety in this setting.

methodsUsing the Club Rhumatismes and Inflammation French network, we conducted a multicentre, retrospective, observational study of patients with cancer diagnosed with inflammatory arthritis under ICI(s) and treated with bDMARD or JAKi. Clinical data were collected using a standardised case report form.

resultsTwenty patients (60% men, median age 69.5 years) were included, with rheumatoid arthritis (RA)-like (n=16), polymyalgia rheumatica-like (n=2) or psoriatic arthritis-like (n=2) clinical presentation. Two patients had pre-existing RA. 90% were treated with glucocorticoids as first-line therapy and 60% received methotrexate prior to bDMARD or JAKi. Anti-interleukin-6 receptor (IL-6R) therapy was used in 13/20 patients (65%), leading to clinical improvement in 11/13 patients (85%), but one patient experienced intestinal perforation and cancer progression was noticed in 6/13 patients (46%). Tumour necrosis factor inhibitors were used in 5/20 patients (25%), with improvement in 4/5 patients (80%) and cancer progression was observed in 3/5 patients (60%). Two infections (diverticulitis and pneumonitis) were reported. Anakinra, baricitinib and ustekinumab were each used in one patient. Median duration of the bDMARD or JAKi was 17 weeks.

conclusionAnti-IL-6R therapy is currently the most common strategy in patients with ICI-induced inflammatory arthritis and insufficient response to glucocorticoids and methotrexate, leading to improvement in >80%. Overall, cancer progression occurred in about half of patients and whether the bDMARD/JAKi impacted the tumour response remains to be determined.

Indexed as

Antirheumatic AgentsArthritis, RheumatoidJanus Kinase InhibitorsAgedDrug Therapy, CombinationFemaleGlucocorticoidsHumansImmune Checkpoint InhibitorsInterleukin 1 Receptor Antagonist ProteinMaleMethotrexateRetrospective StudiesTumor Necrosis Factor InhibitorsUstekinumabAntirheumatic AgentsGlucocorticoidsImmune Checkpoint InhibitorsInterleukin 1 Receptor Antagonist ProteinJanus Kinase InhibitorsMethotrexateTumor Necrosis Factor InhibitorsUstekinumabarthritisbiological therapyimmune system diseasestherapeutics

Identifiers

PMID36270747
PMCPMC9594531
OpenAlexW4307046930

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.