Evidence map›Paper›PMID 36254804›Full record

Observational studyCancer control : journal of the Moffitt Cancer Center

A Retrospective Cohort Study of Multiple Immune-Related Adverse Events and Clinical Outcomes Among Patients With Cancer Receiving Immune Checkpoint Inhibitors.

Hiroki Hata, Chikako Matsumura, Yugo Chisaki, Kae Nishioka, Misaki Tokuda, Kazuyo Miyagi, Tomoki Suizu, Yoshitaka Yano

Open access · goldAbstract readObservational Study
In one paragraph

Observational study in Cancer control : journal of the Moffitt Cancer Center. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.6field-weighted citation impact, top 15% 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

14 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
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  3. Review
  4. Review
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  6. Article
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  11. [Advances in Predictive Research of Immune Checkpoint Inhibitors-related 
Adverse Events].Zhongguo fei ai za zhi = Chinese journal of lung cancer · 2023
    Article
  12. Article
  13. Clonally expanded, thyrotoxic effector CD8Science translational medicine · 2023
    Article
  14. 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

8 authors at 2 institutions in 1 country.

Hiroki HataEducation and Research Center for Clinical Pharmacy, 12916Kyoto Pharmaceutical University, Kyoto, Japan.
Chikako MatsumuraEducation and Research Center for Clinical Pharmacy, 12916Kyoto Pharmaceutical University, Kyoto, Japan.
Yugo ChisakiEducation and Research Center for Clinical Pharmacy, 12916Kyoto Pharmaceutical University, Kyoto, Japan.ORCID 0000-0002-3492-8291
Kae NishiokaEducation and Research Center for Clinical Pharmacy, 12916Kyoto Pharmaceutical University, Kyoto, Japan.
Misaki TokudaEducation and Research Center for Clinical Pharmacy, 12916Kyoto Pharmaceutical University, Kyoto, Japan.
Kazuyo MiyagiDepartment of Pharmacy, 13707National Hospital Organization Osaka National Hospital, Osaka, Japan.
Tomoki SuizuDepartment of Pharmacy, 13707National Hospital Organization Osaka National Hospital, Osaka, Japan.
Yoshitaka YanoEducation and Research Center for Clinical Pharmacy, 12916Kyoto Pharmaceutical University, Kyoto, Japan.ORCID 0000-0001-7787-883X
Kyoto Pharmaceutical University · JPOsaka National Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectivesImmune checkpoint inhibitors (ICIs) are effective in various types of cancer and cause immune-related adverse events (irAEs). The occurrence of irAEs is associated with improved survival outcome. We investigated the association between the occurrence of irAEs and overall survival (OS) and progression free survival (PFS), and the risk factors for the development of irAEs, in patients with non-small-cell lung cancer (NSCLC), gastric cancer (GC) and melanoma (MM) treated with ICIs.

methodsThis was a retrospective observational cohort study, and the data were taken from inpatients in a hospital. OS and PFS were compared among patients with different numbers of irAEs. Log-rank test and Cox regression and logistic regression analysis were applied, and details of irAEs characteristics were summarized.

resultsWe obtained data from 200 patients. The major tumor types were NSCLC, GC, and MM. Median OS and PFS in all patients were 9.3 and 3.5 months, respectively. Patients without irAEs tended to have shorter OS or PFS compared with those with a single irAE or multi-system irAEs. Covariate analysis suggested that age (≥75 years), albumin (≥3.5 g/dL) and smoking history were significant for increased occurrence of irAEs. Pneumonitis and thyroiditis tended to occur frequently in patients with NSCLC and MM. The irAE grade was ≤2 in 67.3% of all irAEs, and days of irAEs onset varied.

conclusionWe observed patients with irAEs tended to have better OS or PFS in patients with various types of cancers treated with ICIs. We suggest that ICIs should be used appropriately by continuously monitoring the irAEs.

Indexed as

Carcinoma, Non-Small-Cell LungImmune Checkpoint InhibitorsLung NeoplasmsMelanomaStomach NeoplasmsAgedAlbuminsAntineoplastic Agents, ImmunologicalCohort StudiesHumansNivolumabRetrospective StudiesAlbuminsAntineoplastic Agents, ImmunologicalImmune Checkpoint InhibitorsNivolumabclinical outcomesimmune checkpoint inhibitorslong-term immune-related adverse eventsmultiple immune-related adverse events

Identifiers

PMID36254804
PMCPMC9583223
OpenAlexW4306731862

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.