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CAR-T 治疗后经 (18)F-FDG PET/CT 检出的儿童 B 细胞急性淋巴细胞白血病乳腺复发

英文原题:Breast Relapse of Pediatric B-Cell Acute Lymphoblastic Leukemia After CAR-T Therapy Detected by (18)F-FDG PET/CT.

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Breast Relapse of Pediatric B-Cell Acute Lymphoblastic Leukemia After CAR-T Therapy Detected by (18)F-FDG PET/CT.

PubMed 2024/05/01(内容时间) Anticancer Res Q4 · IF 1.8(JCR 2025)

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研究概要

据我们所知,这是首例关于儿童 B-ALL 患者在 CAR-T 治疗后出现孤立且隐匿性乳腺复发的报告,该复发在疾病监测期间通过 18 F-FDG PET/CT 早期发现。

研究思路结论见上方概要

B细胞急性淋巴细胞白血病(B-ALL)是儿童最常见的恶性肿瘤。在采用标准化疗免疫疗法以及近年来嵌合抗原受体(CAR)-T细胞治疗的B-ALL儿科患者中,髓内和髓外疾病复发是众所周知的现象。18F-氟脱氧葡萄糖正电子发射断层扫描/计算机断层扫描(18F-FDG PET/CT)作为一种敏感的影像学工具,用于检测髓外部位的疾病复发,但在CAR-T 治疗背景下的文献证据有限。病例报告:一名12岁女性因B-ALL复发接受CAR-T 治疗,在疾病缓解后进行监测性18F-FDG PET/CT扫描,检测到乳腺实质中一处孤立且临床隐匿的复发灶,并经组织学证实。

展开英文摘要原文

B-cell acute lymphoblastic leukemia (B-ALL) is the most common childhood malignancy. Medullary and extramedullary disease relapse is a well-known occurrence in B-ALL pediatric patients treated with standard chemo-immunotherapy and, more recently, with chimeric antigen receptor (CAR)-T cell therapy. 18 F-Fluorodeoxyglucose positron emission tomography/computed tomography ( 18 F-FDG PET/CT) emerges as a sensitive imaging tool for detecting disease relapse at extra-medullary sites, with only limited literature evidence in the CAR-T therapy setting. CASE REPORT: In a 12-year-old female treated with CAR-T therapy for B-ALL relapse, 18 F-FDG PET/CT scan performed for surveillance, after disease remission, detected a solitary and clinically occult relapse in the breast parenchyma that was histologically confirmed.

At our knowledge, this is the first report about a pediatric B-ALL patient with a solitary and occult breast relapse after CAR-T therapy, early discovered by 18 F-FDG PET/CT during disease monitoring.

论文信息

作者
Perrone E、Taralli S、Pagliara D、Larocca LM、Vinti L、Leccisotti L
单位
Nuclear Medicine Unit, Department of Diagnostic Imaging, Radiation Oncology and Hematology, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy.Italy
文献类型
病例报告
期刊
Anticancer research2024 May
原文标识
PubMed 38677722 · DOI 10.21873/anticanres.17032