Evidence map›Paper›PMID 39795946›Full record

ReviewInternational journal of molecular sciences2024

Immune Checkpoint Inhibitor-Associated Cutaneous Adverse Events: Mechanisms of Occurrence.

Abdulaziz M Eshaq, Thomas W Flanagan, Abdulqader A Ba Abbad, Zain Alabden A Makarem, Mohammed S Bokir, Ahmed K Alasheq, Sara A Al Asheikh, Abdullah M Almashhor, Faroq Binyamani, Waleed A Al-Amoudi and 4 more

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Review
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  7. Immune checkpoint inhibitor associated lichenoid eruptions: a review of non-steroidal systemic maintenance therapies.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2025
    Review
  8. 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

14 authors.

Abdulaziz M EshaqDepartment of Epidemiology and Biostatstics, Milken Institute School of Public Health, George Washington University Washington, Washington, DC 20052, USA.
Thomas W FlanaganDepartment of Pharmacology and Experimental Therapeutics, LSU Health Sciences Center, New Orleans, LA 70112, USA.
Abdulqader A Ba AbbadCollege of Medicine, Alfaisal University, Riyadh 11533, Saudi Arabia.
Zain Alabden A MakaremCollege of Medicine, Alfaisal University, Riyadh 11533, Saudi Arabia.
Mohammed S BokirCollege of Medicine, Alfaisal University, Riyadh 11533, Saudi Arabia.
Ahmed K AlasheqCollege of Medicine, Alfaisal University, Riyadh 11533, Saudi Arabia.
Sara A Al AsheikhCollege of Medicine, Alfaisal University, Riyadh 11533, Saudi Arabia.
Abdullah M AlmashhorCollege of Medicine, Alfaisal University, Riyadh 11533, Saudi Arabia.
Faroq BinyamaniCollege of Medicine, Alfaisal University, Riyadh 11533, Saudi Arabia.
Waleed A Al-AmoudiCollege of Medicine, Alfaisal University, Riyadh 11533, Saudi Arabia.
Abdulaziz S BawzirDepartment of Radiology, King Saud Medical City, Riyadh 11533, Saudi Arabia.
Youssef HaikelInstitut National de la Santé et de la Recherche Médicale, University of Strasbourg, 67000 Strasbourg, France.
Mossad MegahedClinic of Dermatology, University Hospital of Aachen, 52074 Aachen, Germany.
Mohamed HassanResearch Laboratory of Surgery-Oncology, Department of Surgery, Tulane University School of Medicine, New Orleans, LA 70112, USA.ORCID 0000-0002-0336-6425

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immunotherapy, particularly that based on blocking checkpoint proteins in many tumors, including melanoma, Merkel cell carcinoma, non-small cell lung cancer (NSCLC), triple-negative breast (TNB cancer), renal cancer, and gastrointestinal and endometrial neoplasms, is a therapeutic alternative to chemotherapy. Immune checkpoint inhibitor (ICI)-based therapies have the potential to target different pathways leading to the destruction of cancer cells. Although ICIs are an effective treatment strategy for patients with highly immune-infiltrated cancers, the development of different adverse effects including cutaneous adverse effects during and after the treatment with ICIs is common. ICI-associated cutaneous adverse effects include mostly inflammatory and bullous dermatoses, as well as severe cutaneous side reactions such as rash or inflammatory dermatitis encompassing erythema multiforme; lichenoid, eczematous, psoriasiform, and morbilliform lesions; and palmoplantar erythrodysesthesia. The development of immunotherapy-related adverse effects is a consequence of ICIs' unique molecular action that is mainly mediated by the activation of cytotoxic CD4

Indexed as

Immune Checkpoint InhibitorsNeoplasmsSkin DiseasesHumansImmunotherapyProgrammed Cell Death 1 ReceptorImmune Checkpoint InhibitorsProgrammed Cell Death 1 ReceptorCAR T cellsCTLA-4ICIsPD-1

Identifiers

PMID39795946
PMCPMC11719825

What OpenQuestion holds

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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.