Evidence map›Paper›PMID 38126033›Full record

Observational studyOncoimmunology2023

Safety and effectiveness of combination versus monotherapy with immune checkpoint inhibitors in patients with preexisting autoimmune diseases.

Pankti Reid, Sabina Sandigursky, Juhee Song, Maria A Lopez-Olivo, Houssein Safa, Samuel Cytryn, Elizaveta Efuni, Maryam Buni, Anna Pavlick, Michelle Krogsgaard and 7 more

Open access · goldAbstract readObservational StudyMulticenter Study
In one paragraph

Observational study in Oncoimmunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 14% 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 7 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. The management of rheumatic immune related adverse events.Best practice & research. Clinical rheumatology · 2026
    Review
  4. Article
  5. Review
  6. Article
  7. Review
  8. Review
  9. Article
  10. 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

17 authors at 6 institutions in 2 countries.

Pankti ReidDivision of Rheumatology, Department of Medicine, University of Chicago Medical Center, Chicago, IL, USA.ORCID 0000-0002-7645-0919
Sabina SandigurskyDivision of Rheumatology, Department of Medicine, NYU Langone Health, New York, NY, USA.
Juhee SongDepartment of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Maria A Lopez-OlivoDepartment of Health Services Research, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Houssein SafaDepartment of Melanoma Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Samuel CytrynDivision of Internal Medicine, Department of Medicine, NYU Langone Health, New York, TX, USA.
Elizaveta EfuniDivision of Internal Medicine, Department of Medicine, NYU Langone Health, New York, TX, USA.
Maryam BuniSection of Rheumatology and Clinical Immunology, Department of General Internal Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Anna PavlickMedical Oncology, Weill Cornell Medical Center, New York, NY, USA.
Michelle KrogsgaardPerlmutter Cancer Center, Department of Pathology, NYU Langone Health, New York, NY, USA.
Osama Abu-ShawerDepartment of Internal Medicine, Harvard Medical School, Boston, MA, USA.
Mehmet AltanDepartment of Thoracic/Head and Neck Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Jeffrey S WeberPerlmutter Cancer Center, Department of Medicine, NYU Langone Health, New York, NY, USA.
Osama E RahmaDepartment of Internal Medicine, Harvard Medical School, Boston, MA, USA.
Maria E Suarez-AlmazorDepartment of Health Services Research, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Adi DiabDepartment of Melanoma Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Noha Abdel-WahabDepartment of Melanoma Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
The University of Texas MD Anderson Cancer Center · USNYU Langone Health · USBrigham and Women's Hospital · USCleveland Clinic · USCornell University · USUniversity of Chicago Medical Center · US

Funding

Project 4P50CA225450 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI OSMAN, IMAN · 2019 to 2025
$12.5M
Institutional Career Development Core (Chapter 1)KL2TR002387 · NCATS · UNIVERSITY OF CHICAGO · PI ERIC C BEYER, Lisa L Barnes · 2017 to 2026
$7.6M
T-cell intrinsic mechanisms of resistance to PD-1 checkpoint blockadeR01CA243486 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI KROGSGAARD, MICHELLE, ZHU, CHENG · 2020 to 2024
$3.5M
(PQ8) Predicting immune-related toxicity in the adjuvant melanoma setting with checkpoint inhibitionR01CA231295 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI OSMAN, IMAN, WEBER, JEFFREY S · 2018 to 2022
$2.4M
Improving decision-making in patients with resectable melanoma and pre-existing autoimmune disease considering immune checkpoint inhibitionK08CA237619 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI LOPEZ-OLIVO, MARIA DE LOS ANGELES · 2020 to 2024
$938k
Immune-Related Adverse Events in Melanoma Patients Receiving Adjuvant Immune Checkpoint Inhibitor TherapyK01AI163412 · NIAID · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI HASSAN, NOHA ABDELWAHAB HASSAN ALI · 2021 to 2025
$569k
NCATS NIH HHS KL2 TR002387NCI NIH HHS K08 CA237619NCI NIH HHS P50 CA225450NCI NIH HHS R01 CA231295NCI NIH HHS R01 CA243486NIAID NIH HHS K01 AI163412
6 · The paper itself

Abstract

Patients with preexisting autoimmune disease (pAID) are generally excluded from clinical trials for immune checkpoint inhibitors (ICIs) for cancer due to concern of flaring pAID. In this multi-center, retrospective observational study, we compared safety of ICI combination (two ICI agents) versus monotherapy in cancer patients with pAIDs. The primary outcome was time to AEs (immune-related adverse events (irAEs) and/or pAID flares), with progression-free survival (PFS) and overall survival as secondary outcomes. Sixty-four of 133 patients (48%) received ICI combination and 69 (52%) monotherapy. Most had melanoma (32%) and lung cancer (31%). Most common pAIDs were rheumatic (28%) and dermatologic (23%). Over a median follow-up of 15 months (95%CI, 11-18 mo), the cumulative incidence of any-grade irAEs was higher for combination compared to monotherapy (subdistribution hazard ratio (sHR) 2.27, 95%CI 1.35-3.82). No statistically significant difference was observed in high-grade irAEs (sHR 2.31 (0.95-5.66),

Indexed as

Autoimmune DiseasesLung NeoplasmsMelanomaHumansImmune Checkpoint InhibitorsImmune Checkpoint Inhibitorsautoimmune disease flarecancer immunotherapy toxicitycombination immune checkpoint inhibitorimmune-related adverse eventsPreexisting autoimmune disease

Identifiers

PMID38126033
PMCPMC10732692
OpenAlexW4388109000

What OpenQuestion holds

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LicenceCC BY-NC
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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.