Evidence map›Paper›PMID 33680877›Full record

ArticleWorld journal of clinical oncology2021

Racial disparities in immune-related adverse events of immune checkpoint inhibitors and association with survival based on clinical and biochemical responses.

Monica Peravali, Cristiane Gomes-Lima, Eshetu Tefera, Mairead Baker, Mamta Sherchan, Saira Farid, Kenneth Burman, Florina Constantinescu, Irina Veytsman

Abstract read
In one paragraph

Article in World journal of clinical oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
–field-weighted citation impact
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

24 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Pharmacoequity measurement framework: A tool to reduce health disparities.Journal of managed care & specialty pharmacy · 2025
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

9 authors.

Monica PeravaliDepartment of Hematology/Oncology, MedStar Washington Hospital Center, Washington, DC 20010, United States. monica.peravali@medstar.net.
Cristiane Gomes-LimaDepartment of Endocrinology, MedStar Washington Hospital Center, Washington, DC 20010, United States.
Eshetu TeferaDepartment of Biostatistics and Bioinformatics, MedStar Health Research Institute, Washington, DC 20010, United States.
Mairead BakerDepartment of Internal Medicine, MedStar Washington Hospital Center, Washington, DC 20010, United States.
Mamta SherchanDepartment of Rheumatology, MedStar Washington Hospital Center, Washington, DC 20010, United States.
Saira FaridDepartment of Internal Medicine, MedStar Washington Hospital Center, Washington, DC 20010, United States.
Kenneth BurmanDepartment of Endocrinology, MedStar Washington Hospital Center, Washington, DC 20010, United States.
Florina ConstantinescuDepartment of Rheumatology, MedStar Washington Hospital Center, Washington, DC 20010, United States.
Irina VeytsmanDepartment of Hematology/Oncology, MedStar Washington Hospital Center, Washington, DC 20010, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundImmune checkpoint inhibitors (ICPi) cause various immune-related adverse events

aimTo evaluate the association between development of irAE and survival outcomes among a racially diverse patient population.

methodsData on patients with stage IV solid malignancies treated with programmed cell death-protein 1/programmed death ligand 1 blockers between January 2013 and December 2018 across MedStar Georgetown Cancer Institute facilities were retrospectively reviewed. Patients treated with cytotoxic T-lymphocyte-associated protein 4 inhibitors were excluded. Progression free survival (PFS) and overall survival (OS) were primary endpoints and were calculated using Kaplan-Meier methods and Wilcoxon rank sum test for comparison.

resultsOut of 293 patients who met eligibility criteria, 91 pts (31%) had any grade irAE; most common AE were endocrine (40.7%) specifically TSH elevation, dermatological (23.1%) and rheumatologic (18.7%). Proportion of irAE was significantly higher in Caucasians

conclusionDevelopment of irAE positively correlated with improved PFS and OS as reported in previous studies. To our knowledge, this is the first study observing differences in OS favoring endocrine AE and Caucasian race. These factors may be potential surrogate markers of prognosis pending replication of these results in large-scale studies.

Indexed as

Adverse eventsEndocrineImmunotherapyMinorityRaceSurvival

Identifiers

PMID33680877
PMCPMC7918525

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.