Evidence map›Paper›PMID 35188215›Full record

ArticleJournal of the National Cancer Institute2022

Pre-Existing Autoimmune Disease and Mortality in Patients Treated with Anti-PD-1 and Anti-PD-L1 Therapy.

Kimberly Tang, Bruce C Tiu, Guihong Wan, Shijia Zhang, Nga Nguyen, Bonnie Leung, Alexander Gusev, Kerry L Reynolds, Shawn G Kwatra, Yevgeniy R Semenov

Open access · greenAbstract read
In one paragraph

Article in Journal of the National Cancer Institute, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 2 pooled it
1.9field-weighted citation impact, top 13% 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

17 citing papers in PubMed, 2 syntheses or guidelines pooled it, 19 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
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  9. Care settings of transient ischemic attack in the United States: A cohort study from the TriNetX health research network.Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association · 2024
    Article
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  13. 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

10 authors at 4 institutions in 1 country.

Kimberly TangDepartment of Dermatology, Massachusetts General Hospital, Boston, MA, USA.ORCID 0000-0002-7718-2872
Bruce C TiuDepartment of Dermatology, Massachusetts General Hospital, Boston, MA, USA.
Guihong WanDepartment of Dermatology, Massachusetts General Hospital, Boston, MA, USA.
Shijia ZhangDepartment of Dermatology, Massachusetts General Hospital, Boston, MA, USA.
Nga NguyenDepartment of Dermatology, Massachusetts General Hospital, Boston, MA, USA.
Bonnie LeungDepartment of Dermatology, Massachusetts General Hospital, Boston, MA, USA.
Alexander GusevDepartment of Medicine, Dana Farber Cancer Institute, Boston, MA, USA.
Kerry L ReynoldsDepartment of Medicine, Division of Oncology, Massachusetts General Hospital, Boston, MA, USA.
Shawn G KwatraDepartment of Dermatology, Johns Hopkins University, Baltimore, MD, USA.
Yevgeniy R SemenovDepartment of Dermatology, Massachusetts General Hospital, Boston, MA, USA.ORCID 0000-0002-7387-3094
Harvard University · USMassachusetts General Hospital · USDana-Farber Cancer Institute · USJohns Hopkins University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although indications for immune checkpoint inhibitors (ICIs) have dramatically increased in the past decade, ICIs have been associated with autoinflammatory immune-related adverse events, which can resemble autoimmune diseases (ADs). Little is known about the impact of baseline AD on mortality in cancer patients treated with ICIs. Here, we identified 17 497 patients with preexisting autoimmune diagnoses prior to treatment with antiprogrammed cell death receptor-1 or antiprogrammed cell death ligand-1 therapy and 17 497 matched controls through the TriNetX Diamond network of more than 200 million patients across the United States and Europe. Using a Cox proportional hazards model, we found that patients with history of AD were not at higher risk of mortality than non-AD patients (hazard ratio [HR] = 1.03, 95% confidence interval [CI] = 1 to 1.07; P = .05). Additionally, history of Hashimoto disease (HR = 0.75, 95% CI = 0.62 to 0.90; P = .002) and vitiligo (HR = 0.52, 95% CI = 0.34 to 0.81; P = .003) were statistically significantly associated with decreased mortality. This suggests that underlying AD need not be a contraindication to inclusion in clinical trials and administration of ICI for treatment of cancer.

Indexed as

Antineoplastic Agents, ImmunologicalAutoimmune DiseasesNeoplasmsB7-H1 AntigenHumansProgrammed Cell Death 1 ReceptorUnited StatesAntineoplastic Agents, ImmunologicalB7-H1 AntigenCD274 protein, humanProgrammed Cell Death 1 Receptor

Identifiers

PMID35188215
PMCPMC9360452
OpenAlexW4212830566

What OpenQuestion holds

Textmetadata
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.