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:Sweet-like syndrome secondary to chimeric antigen receptor T-cell therapy for multiple myeloma: a case report.
Sweet-like syndrome secondary to chimeric antigen receptor T-cell therapy for multiple myeloma: a case report.
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靶向B细胞成熟抗原的CAR-T 细胞(BCMA CAR-T)疗法显著改善了复发/难治性多发性骨髓瘤(R/R MM)的治疗结局,但其免疫相关不良事件谱仍在不断界定。其中,皮肤毒性并不少见,却常未得到充分关注;尤其迟发性皮肤反应可能报告不足。 病例报告:我们报告一例R/R MM患者接受BCMA CAR-T 治疗后达到严格意义的完全缓解(sCR),并于输注后第50天出现迟发性皮损。组织病理显示真皮内大量中性粒细胞浸润,符合Sweet综合征。然而,患者缺乏发热、关节痛或外周血中性粒细胞增多等典型临床表现,因此诊断为CAR-T 治疗相关“Sweet样综合征”。未给予全身性糖皮质激素,皮损自行消退。
据我们所知,此前几乎没有BCMA CAR-T 治疗后发生Sweet综合征或Sweet样综合征的病例报道。本病例拓展了已知CAR-T 相关皮肤不良事件谱,并强调对于非典型迟发性皮疹,应尽早活检,而非经验性使用全身皮质类固醇,以指导恰当处理。
Chimeric antigen receptor T-cell therapy targeting B-cell maturation antigen (BCMA CAR-T) has significantly improved outcomes in relapsed/refractory multiple myeloma (R/RMM), yet its spectrum of immune-related adverse events continues to be defined. Among these, cutaneous toxicities are not unusual, but frequently receive insufficient attention. Delayed-onset cutaneous reactions, in particular, may be underreported. CASE REPORT: We report a patient with R/RMM who achieved stringent complete response (sCR) following BCMA CAR-T therapy and developed delayed-onset cutaneous lesions on day 50 post-infusion. Histopathology revealed dense dermal neutrophilic infiltration, consistent with Sweet's syndrome. However, the patient lacked typical clinical features such as fever, arthralgia, or peripheral neutrophilia, prompting a diagnosis of 'Sweet-like syndrome' associated with CAR-T therapy. The lesions resolved spontaneously without systemic glucocorticoid therapy.
To our knowledge, virtually no cases of Sweet's syndrome or Sweet-like syndrome have been reported previously after BCMA CAR-T therapy, broadening the recognized spectrum of CAR-T-related cutaneous adverse events and underscoring the importance of early biopsy for atypical, delayed-onset rashes-rather than empiric systemic corticosteroid treatment-to guide appropriate management.
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