Evidence map›Paper›PMID 33616727›Full record

ArticleLung2021

Lessons from Pharmacovigilance: Pulmonary Immune-Related Adverse Events After Immune Checkpoint Inhibitor Therapy.

Stephen W Reese, Eugene Cone, Maya Marchese, Brenda Garcia, Wesley Chou, Asha Ayub, Kerry Kilbridge, Gerald Weinhouse, Quoc-Dien Trinh

Abstract read
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In one paragraph

Article in Lung, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 2 pooled it
0.6field-weighted citation impact, top 30% 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

7 citing papers in PubMed, 2 syntheses or guidelines pooled it, 12 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
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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

9 authors at 3 institutions in 1 country.

Stephen W ReeseDepartment of Surgery, Brigham and Women's Hospital, Center for Surgery and Public Health, Harvard Medical School, Boston, MA, USA.
Eugene ConeDepartment of Surgery, Brigham and Women's Hospital, Center for Surgery and Public Health, Harvard Medical School, Boston, MA, USA.
Maya MarcheseDepartment of Surgery, Brigham and Women's Hospital, Center for Surgery and Public Health, Harvard Medical School, Boston, MA, USA.
Brenda GarciaDepartment of Medicine, Mount Auburn Hospital, Harvard Medical School, Cambridge, MA, USA.
Wesley ChouDepartment of Surgery, Brigham and Women's Hospital, Center for Surgery and Public Health, Harvard Medical School, Boston, MA, USA.
Asha AyubDepartment of Medicine, Mount Auburn Hospital, Harvard Medical School, Cambridge, MA, USA.
Kerry KilbridgeTufts School of Medicine, Boston, MA, USA.
Gerald WeinhouseLank Center for Genitourinary Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Quoc-Dien TrinhDepartment of Surgery, Brigham and Women's Hospital, Center for Surgery and Public Health, Harvard Medical School, Boston, MA, USA. Trinh.qd@gmail.com.ORCID 0000-0003-3857-9276
Brigham and Women's Hospital · USMount Auburn Hospital · USTufts University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo characterize pulmonary toxicities associated with the use of novel immune checkpoint inhibitors

methodsAdverse event reports from immune checkpoint inhibitors targeting PD-1/L1 and CTLA-4 were captured from the W.H.O pharmacovigilance database (VigiBase) up until Dec. 31st 2019 and were analyzed to evaluate for measures of association between the use of immune checkpoint inhibitors and pulmonary toxicities. Disproportionality analysis using both frequentist and Bayesian approaches were used to detect signals between pulmonary immune-related adverse events and the use of these agents.

resultsA total of 9202 adverse pulmonary immune checkpoint inhibitor-related events were captured up until 2019. Adverse pulmonary events were compromised of 1305 airway, 18 alveolar, 5491 interstitial, 898 pleural, 560 vascular and 939 non-specific pulmonary events. We found a common association between all immune checkpoint inhibitors studied and pneumonitis, interstitial lung disease, pulmonary embolism and respiratory failure. We also noted other associations between immune checkpoint inhibitors, however not as uniformly across agents. Most of these immune-related adverse drug reactions were noted to be severe and accounted for a significant source of mortality in the reported cases.

conclusionImmune checkpoint inhibitors are associated with a spectrum of inflammatory pulmonary toxicities. The breadth of pulmonary complications and prevalence may be underappreciated with the use of these agents.

Indexed as

Databases, FactualHumansImmune Checkpoint InhibitorsLung DiseasesPharmacovigilanceRetrospective StudiesImmune Checkpoint InhibitorsImmune checkpoint inhibitorsPleural diseasePneumonitisPulmonary embolismPulmonary pharmacotherapyPulmonary toxicity

Identifiers

PMID33616727
OpenAlexW3130239575

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.