← 返回

R/R T-ALL 中 CD7 CAR-T 桥接 allo-HSCT:病例报告

英文原题:CD7 CAR T bridging to allo-HSCT in R/R T-ALL: A case report.

查看英文原题

CD7 CAR T bridging to allo-HSCT in R/R T-ALL: A case report.

PubMed 2022/07/21(内容时间) Pediatr Transplant Q3 · IF 1.4(JCR 2025)

分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。

研究概要

CD7 CAR-T 细胞桥接 allo-HSCT 是复发/难治性 T-ALL 的一种安全有效方法,可获得持久 CR 和更长的生存期。

中文摘要

难治/复发性T细胞急性淋巴细胞白血病(R/R T-ALL)是一种预后较差的血液系统恶性肿瘤。现有治疗策略未能使大多数患者获益,治疗方法仍在探索中。病例报告:一名8岁男孩经多轮化疗后R/R T-ALL达到完全缓解,随后首次接受异基因造血干细胞移植(allo-HSCT)。遗憾的是,1年3个月后复发。复发后患者接受多轮化疗,但NOTCH1基因和微小残留病灶(MRD)仍为阳性。流式细胞术(FCM)和免疫组化显示CD7异常高表达,因此我们考虑在CD7 CAR-T 细胞治疗后桥接第二次allo-HSCT。该患者毒副作用较低,目前仍处于完全缓解。此病例报告对于R/R T-ALL治疗具有重要意义。

总之,CD7 CAR-T 细胞治疗桥接allo-HSCT是R/R T-ALL的一种安全有效方案,可实现持久完全缓解并延长生存。

展开英文摘要原文

Refractory/relapsed T-cell acute lymphoblastic leukemia (R/R T-ALL) is a hematological malignancy with a poor prognosis. The current treatment strategy has not benefited most patients, and the treatment methods are still being explored. CASE PRESENTATION: An 8-year-old boy with R/R T-ALL achieved CR after multiple chemotherapies, followed by the first allo-HSCT. Unfortunately, 1 year and 3 months later, he relapsed. After recurrence, the patient underwent multiple chemotherapies, but the NOTCH1 gene and MRD were still positive. FCM and immunohistochemistry revealed abnormally high expression of CD7, so we considered bridging the second allo-HSCT after CD7 CAR T-cells treatment. The patient has low toxic and side effects and is still in CR, findings from this case report have more important therapeutic significance for R/R T-ALL.

In conclusion, CD7 CAR T-cells bridging to allo-HSCT is a safe and effective approach for R/R T-ALL, resulting in durable CR and longer survival.

论文信息

作者
Fanqiao M、Chen X、Ren X、Li L、Wu T
第一作者单位
Department of Hematology, Tianjin Medical University General Hospital, Tianjin, China.China
通讯作者单位
Department of Bone Marrow Transplantation, Beijing Boren Hospital, Beijing, China.China
文献类型
病例报告
期刊
Pediatric transplantation2024 May
原文标识
PubMed 35860981 · DOI 10.1111/petr.14367