To evaluate the incidence, type, and timing of cutaneous adverse events (AEs) following CAR T-cell therapy in patients with relapsed or refractory hematologic malignancies, highlighting their clinical significance.
Key Findings:
Cumulative incidence of cutaneous AEs was 11% by 36 months post-CAR-T, indicating a notable occurrence.
Most common cutaneous AEs included maculopapular rash (39%) and pruritic macular rash (22%), which are significant for clinical monitoring.
57% of cutaneous AEs were early-onset, with 22% intermediate-onset and 22% late-onset, suggesting varying mechanisms.
All cutaneous AEs were grade 1 (70%) or grade 2 (30%), indicating a generally low severity.
An increasing number of prior lines of therapy was associated with a lower risk of cutaneous AEs, suggesting a potential area for further investigation.
Interpretation:
Cutaneous AEs following CAR-T therapy are not uncommon and primarily low-grade, with a notable occurrence of late-onset AEs suggesting chronic immune activation, which may have clinical implications for patient management.
Limitations:
Small sample size for multiple myeloma patients (n = 18) may limit generalizability and warrant caution in interpretation.
Retrospective design may introduce bias in data collection and interpretation, and potential confounding factors should be considered.
Conclusion:
Cutaneous AEs occur in approximately 1 in 10 patients following CAR-T therapy, predominantly early and low-grade, but with potential for late occurrences. Further studies are needed to explore the mechanisms behind these findings and their clinical implications.
by Elvira Umyarova, John Sharp, Charles Pei, William Pellegrino, Qiuhong Zhao, Nathan Denlinger, Timothy Voorhees, Marcos De Lima, Narendranath Epperla