Cutaneous adverse events following CAR T-cell therapy in hematologic malignancies - Report - 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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Skin-related adverse effects associated with CAR T-cell therapy in blood cancers

Overview

Cutaneous adverse events (AEs) occur in approximately 11% of patients following CAR T-cell therapy for relapsed or refractory B-cell malignancies. These AEs are predominantly low-grade, with maculopapular rash being the most common, and can present early or late after treatment.

Background

CAR T-cell therapy has revolutionized treatment for relapsed or refractory hematologic malignancies such as diffuse large B-cell lymphoma and B-acute lymphoblastic leukemia. While cytokine release syndrome and neurotoxicity are well-characterized toxicities, cutaneous adverse events remain less understood. This study retrospectively evaluated the incidence, types, and timing of skin-related AEs in patients receiving commercial CAR T-cell products.

Data Highlights

CharacteristicValue
Number of patients analyzed246
Patients with cutaneous AEs (high likelihood)23 (11%)
Median age66 years (range 54–78)
Male patients65%
Median prior therapy lines3 (range 2–7)
Patients with prior autologous HSCT22%
Patients with prior allogeneic HSCT4%
Cutaneous AE typesMaculopapular rash (39%), Pruritic macular rash (22%), Bullous dermatitis (9%), others
Grade of cutaneous AEsGrade 1 (70%), Grade 2 (30%)
Timing of onsetEarly (57%), Intermediate (22%), Late (22%)
Patients treated with topical corticosteroids30%

Key Findings

  • Cutaneous AEs occurred in 11% of patients post-CAR T-cell therapy, predominantly in those treated for B-cell lymphomas and B-ALL; none were observed in multiple myeloma patients.
  • Most cutaneous AEs were low-grade (grade 1 or 2), with maculopapular rash being the most frequent manifestation.
  • The timing of cutaneous AEs varied: 57% early-onset (within 30 days), 22% intermediate (31–180 days), and 22% late-onset (beyond 180 days).
  • Bullous dermatitis, though rare (9%), was observed and resolved without intervention.
  • An inverse association was found between the number of prior therapy lines and risk of cutaneous AEs, suggesting immune competence may influence skin toxicity risk.
  • Topical corticosteroids were used in 30% of affected patients, indicating generally manageable skin toxicity.

Clinical Implications

Clinicians should monitor for cutaneous adverse events following CAR T-cell therapy, as they occur in about one in ten patients and can present early or late post-infusion. Most skin toxicities are low-grade and manageable with topical treatments, but awareness of rare presentations like bullous dermatitis is important. Long-term follow-up is recommended given the potential for delayed skin manifestations.

Conclusion

Cutaneous adverse events are a relatively common and mostly mild complication of CAR T-cell therapy in hematologic malignancies, with variable timing of onset. Recognition and appropriate management can improve patient care during and after CAR T-cell treatment.

References

  1. Pennisi et al. 2023 -- Skin-related adverse effects associated with CAR T-cell therapy in blood cancers

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