Guo Shenrui, Tan Zhen, Guan Wenbin, Yin Yafu
Department of Nuclear Medicine, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Department of Pediatric Hematology/Oncology, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
World J Nucl Med. 2024 Jun 20;23(3):212-216. doi: 10.1055/s-0044-1787537. eCollection 2024 Sep.
Chimeric antigen receptor T-cell (CAR-T) treatment has been widely used in the treatment of hematological malignancies, and its application has been gradually expanded to the research and treatment of solid tumors. However, unconventional types of response may occur after CAR-T treatment, such as hyperprogression, resulting in terrible outcomes. Here, we report the case of a 13-year-old adolescent boy with relapsed and refractory rhabdomyosarcoma who developed early hyperprogression 3 weeks after CAR-T treatment (target: B7H3 and CD171), which was detected by fluorine-18 fluorodeoxyglucose ( F-FDG) positron emission tomography (PET)/computed tomography (CT). The patient eventually underwent amputation. Attention should be paid to the possibility of early hyperprogression after CAR-T treatment, and F-FDG PET/CT has an absolute advantage in early evaluating treatment response to immunotherapy.
嵌合抗原受体T细胞(CAR-T)疗法已广泛应用于血液系统恶性肿瘤的治疗,其应用也逐渐扩展到实体瘤的研究和治疗。然而,CAR-T治疗后可能会出现非常规类型的反应,如疾病超进展,导致严重后果。在此,我们报告1例13岁复发难治性横纹肌肉瘤青少年男性患者,其在CAR-T治疗(靶点:B7H3和CD171)3周后出现早期疾病超进展,通过氟-18氟脱氧葡萄糖(¹⁸F-FDG)正电子发射断层扫描(PET)/计算机断层扫描(CT)检测到。该患者最终接受了截肢手术。应注意CAR-T治疗后早期疾病超进展的可能性,¹⁸F-FDG PET/CT在早期评估免疫治疗反应方面具有绝对优势。