ReviewBMJ open2026
Management of immune-related cutaneous adverse events associated with immune checkpoint inhibitors in patients with cancer: an evidence summary.
Review in BMJ open, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
8 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
objectivesThis study aims to systematically retrieve and synthesise the best available evidence on the management of immune-related cutaneous adverse events (ircAEs) associated with immune checkpoint inhibitors (ICIs) in patients with cancer, thereby providing evidence-based guidance for the development of assessment and management protocols in clinical practice.
designThis study was conducted as an evidence summary following the evidence summary reporting standard of the Fudan University Center for Evidence-Based Nursing. DATA SOURCES: Evidence was searched across clinical decision support resources, guideline repositories, professional society websites and bibliographic databases, including UpToDate, BMJ Best Practice, Joanna Briggs Institute (JBI), National Comprehensive Cancer Network, European Society for Medical Oncology, American Society of Clinical Oncology, Cochrane Library, Embase, PubMed, Web of Science and major Chinese databases. Searches were conducted up to 23 December 2025. ELIGIBILITY CRITERIA: Evidence sources concerning the assessment, prevention or management of ircAEs in adults aged ≥18 years receiving ICIs were eligible. Clinical practice guidelines, expert consensus statements, evidence summaries, systematic reviews, clinical decision support resources and relevant original studies, including observational and quasi-experimental studies, published in Chinese or English were considered for inclusion. Duplicate publications, superseded guidelines and evidence sources that did not meet the predefined methodological quality criteria were excluded. DATA EXTRACTION AND SYNTHESIS: Two reviewers independently screened eligible evidence sources, extracted data and conducted methodological quality appraisal using design-appropriate tools, including the Appraisal of Guidelines for Research and Evaluation II and JBI critical appraisal instruments. Evidence was classified according to the JBI levels of evidence and evaluated for strength of recommendation using the feasibility, appropriateness, meaningfulness and effectiveness framework. Evidence with similar content was compared, integrated and synthesised into practice-oriented evidence statements, with disagreements resolved through discussion or consultation with a third reviewer.
resultsA total of 21 evidence sources were included, comprising nine clinical practice guidelines, five expert consensus statements, two systematic reviews, two evidence summaries, one observational study, one quasi-experimental study and one clinical decision support resource. 29 evidence statements were synthesised across seven domains: risk factor identification, assessment and diagnosis, severity-based treatment, supportive nursing care, follow-up management, patient education and healthcare professional training. The synthesised evidence emphasised baseline skin assessment and early recognition of ircAEs, standardised severity grading, severity-based treatment escalation, phenotype-oriented supportive skin care, structured follow-up, patient and caregiver education, and timely multidisciplinary referral for severe or complex cutaneous toxicities.
conclusionsThe evidence provides a structured basis for standardising ircAEs screening, nursing assessment, symptom management, referral and follow-up in patients receiving ICIs. It may also support oncology nurses in strengthening patient and caregiver education, promoting timely symptom reporting and self-management and facilitating multidisciplinary referral for severe or atypical cutaneous toxicities.
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