CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Toxic epidermal necrolysis-like cutaneous toxicity following chimeric antigen receptor T-cell therapy in recurrent large B-cell lymphoma.
Toxic epidermal necrolysis-like cutaneous toxicity following chimeric antigen receptor T-cell therapy in recurrent large B-cell lymphoma.
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CAR-T 治疗多种B细胞恶性肿瘤疗效显著,但可能引起CRS和血细胞减少。本文报告一例69岁弥漫大B细胞淋巴瘤男性接受阿基仑赛后出现罕见严重皮肤毒性,表现类似中毒性表皮坏死松解症。患者持续发热并发生CRS,随后出现广泛红斑样皮疹并进展为水疱和大疱。因近期使用别嘌醇,曾考虑药物诱发的表皮坏死松解症,但起病时间和黏膜受累轻微均不符合典型表现。该皮肤反应不同于典型Stevens-Johnson综合征/表皮坏死松解症,且与细胞因子风暴同时发生。尽管缺少诊疗指南,患者经全身糖皮质激素治疗后明显改善。该病例扩展了CAR-T 相关皮肤毒性谱,提示皮肤科医生需早期识别组织病理表现并制定个体化管理。
Chimeric antigen receptor (CAR) T-cell therapy has demonstrated remarkable success in treating various B-cell malignancies, redirecting T-cell cytotoxicity toward cancer cells. Despite its efficacy, CAR-T therapy is associated with potential risks, including cytokine release syndrome (CRS) and cytopenia.
We present a case of a 69-year-old man with diffuse large B-cell lymphoma treated with axicabtagene-ciloleucel CAR-T therapy, who developed a rare and severe cutaneous toxicity resembling toxic epidermal necrolysis (TEN). The patient exhibited persistent fevers, CRS, and subsequent development of a widespread erythematous macular eruption, progressing to vesiculation with bullae.
Notably, allopurinol-induced TEN was considered with the patient's recent exposure to allopurinol, although the onset and minimal mucosal involvement did not align with typical presentations of allopurinol-induced cases. The cutaneous reaction, distinct from typical SJS/TEN, showed minimal mucosal involvement and coincided with the cytokine release storm, differing from allopurinol-induced TEN.
Despite the absence of guidelines, the patient was managed with systemic steroids, achieving significant improvement. This case expands the spectrum of CAR-T therapy-related cutaneous toxicities, highlighting the need for early recognition of histopathology and tailored management by dermatologists.
Further understanding of these reactions is crucial for optimizing the safety profile of this groundbreaking immunotherapy.
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