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Published on: March 8, 2022
Detection of novel therapies using a multi-national, multi-institutional registry of cutaneous immune-related adverse
Rohan Mital1,2, Tracey S Otto3,4, Andrei Savu1
1The Ohio State University College of Medicine, Columbus, OH, USA.
Background:
Cutaneous immune-related adverse events (cirAEs) remain a prevalent and common sequelae of immune checkpoint inhibitor (ICI) therapy, often necessitating treatment interruption and prolonged immune suppression. Treatment algorithms are still poorly defined, based on single-institution case reports without adequate safety assessments, and subject to publication bias.
Methods:
Data in this registry were collected through a standardized REDCap form distributed to dermatologists via email listserv.
Results:
Ninety-seven cirAEs were reported from 13 institutions in this registry. Topical and systemic steroids were the most common treatments used; however, targeted treatment matched to disease morphology was identified at numerous sites. Novel cirAE therapy uses that to our knowledge have not been previously described were captured including tacrolimus for the treatment of follicular, bullous, and eczematous eruptions and phototherapy for eczematous eruptions. Moreover, further evidence of cirAE treatment applications sparsely described in literature were also captured in this study including dupilumab and rituximab for bullous eruptions, phototherapy for lichenoid and psoriasiform eruptions, and acitretin for psoriasiform eruptions, among others. No serious adverse events were reported. Numerous targeted therapeutics including dupilumab, rituximab, and psoriasis biologics, among others, were associated with a cirAE grade improvement of ≥2 grades in every patient treated.
Conclusion:
This study suggests that a multi-institutional registry of cirAEs and management is not only feasible but that the information collected can be used to detect, evaluate, and rigorously assess targeted treatments for cirAEs. Further expansion and modification to include treatment progression may allow for sufficient data for specific treatment recommendations to be made.
Insights
This study highlights novel and effective treatments for cutaneous immune-related adverse events (cirAEs) from immune checkpoint inhibitor (ICI) therapy. A multi-institutional registry demonstrated feasibility and identified targeted therapies improving cirAEs with no serious adverse events.
Area of Science:
- Dermatology
- Oncology
- Immunology
Background:
- Cutaneous immune-related adverse events (cirAEs) are common side effects of immune checkpoint inhibitor (ICI) therapy.
- Current treatment guidelines for cirAEs are poorly defined and lack robust safety data.
- Existing treatment algorithms often rely on limited case reports and may be subject to publication bias.
Purpose of the Study:
- To establish a multi-institutional registry for collecting data on cirAEs and their management.
- To identify and evaluate targeted treatment strategies for various cirAE morphologies.
- To assess the feasibility and utility of a collaborative approach to cirAE management.
Main Methods:
- A registry was established using a standardized REDCap form.
- Data were collected from 13 institutions, documenting 97 cases of cirAEs.
- Dermatologists distributed the data collection form via email listservs.
Main Results:
- Topical and systemic steroids were frequently used, but targeted therapies matched to disease presentation were also identified.
- Novel treatments like tacrolimus for follicular, bullous, and eczematous eruptions, and phototherapy for eczematous eruptions were documented.
- Effective use of dupilumab and rituximab for bullous eruptions, phototherapy for lichenoid/psoriasiform eruptions, and acitretin for psoriasiform eruptions were observed.
- Targeted therapeutics, including dupilumab, rituximab, and psoriasis biologics, led to significant grade improvement (≥2) in all treated patients.
- No serious adverse events were reported during the study.
Conclusions:
- A multi-institutional registry for cirAEs and their management is feasible and valuable.
- Collected data can effectively identify, evaluate, and assess targeted treatments for cirAEs.
- Further registry expansion to include treatment progression can inform specific treatment recommendations for cirAEs.
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