Cutaneous adverse events following CAR T-cell therapy in hematologic malignancies - Summary - MDSpire

Cutaneous adverse events following CAR T-cell therapy in hematologic malignancies

  • By

  • Elvira Umyarova

  • John Sharp

  • Charles Pei

  • William Pellegrino

  • Qiuhong Zhao

  • Nathan Denlinger

  • Timothy Voorhees

  • Marcos De Lima

  • Narendranath Epperla

  • March 12, 2026

  • 0 min

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Objective:

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.

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