Evidence map›Paper›PMID 35223483›Full record

ReviewFrontiers in oncology2022

Mechanism of Lethal Skin Toxicities Induced by Epidermal Growth Factor Receptor Inhibitors and Related Treatment Strategies.

Yanping Li, Ruoqiu Fu, Tingting Jiang, Dongyu Duan, Yuanlin Wu, Chen Li, Ziwei Li, Rui Ni, Li Li, Yao Liu

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed, 1 pooled it
4.6field-weighted citation impact, top 4% 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

41 citing papers in PubMed, 1 synthesis or guideline pooled it, 50 citations in OpenAlex.

  1. Pooled it
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  14. Aprepitant: Review on Solubility Enhancement.Recent advances in drug delivery and formulation · 2026
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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 2 institutions in 1 country.

Yanping LiDepartment of Pharmacy, Daping Hospital, Army Medical University, Chongqing, China.
Ruoqiu FuDepartment of Pharmacy, Daping Hospital, Army Medical University, Chongqing, China.
Tingting JiangDepartment of Pharmacy, Daping Hospital, Army Medical University, Chongqing, China.
Dongyu DuanDepartment of Pharmacy, Daping Hospital, Army Medical University, Chongqing, China.
Yuanlin WuDepartment of Pharmacy, Daping Hospital, Army Medical University, Chongqing, China.
Chen LiDepartment of Pharmacy, Daping Hospital, Army Medical University, Chongqing, China.
Ziwei LiDepartment of Pharmacy, Daping Hospital, Army Medical University, Chongqing, China.
Rui NiDepartment of Pharmacy, Daping Hospital, Army Medical University, Chongqing, China.
Li LiDepartment of Pharmacy, Daping Hospital, Army Medical University, Chongqing, China.
Yao LiuDepartment of Pharmacy, Daping Hospital, Army Medical University, Chongqing, China.
Army Medical University · CNDaping Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Epidermal growth factor receptor (EGFR) inhibitors are widely used to treat various types of cancers such as non-small cell lung cancer, head and neck cancer, breast cancer, pancreatic cancer. Adverse reactions such as skin toxicity, interstitial lung disease, hepatotoxicity, ocular toxicity, hypomagnesemia, stomatitis, and diarrhea may occur during treatment. Because the EGFR signaling pathway is important for maintaining normal physiological skin function. Adverse skin reactions occurred in up to 90% of cancer patients treated with EGFR inhibitors, including common skin toxicities (such as papulopustular exanthemas, paronychia, hair changes) and rare fatal skin toxicities (e.g., Stevens-Johnson syndrome, toxic epidermal necrolysis, acute generalized exanthematous pustulosis). This has led to the dose reduction or discontinuation of EGFR inhibitors in the treatment of cancer. Recently, progress has been made about research on the skin toxicity of EGFR inhibitors. Here, we summarize the mechanism of skin toxicity caused by EGFR inhibitors, measures to prevent severe fatal skin toxicity, and provide reference for medical staff how to give care and treatment after adverse skin reactions.

Indexed as

drug induced diseaseEGFR inhibitorslethal skin toxicitiespreventive measurestreatment strategies

Identifiers

PMID35223483
PMCPMC8866822
OpenAlexW4211219835

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.