决定异体 CAR T 细胞排斥与扩增的细胞和分子机制
Cellular and molecular mechanisms determining allogeneic CAR T cell rejection and expansion.
我们评估了11例接受单一批次cemacabtagene ansegedleucel(cema-cel)治疗的大B细胞淋巴瘤患者,cemacabtagene ansegedleucel是一种异体抗CD19 CAR T产品。
英文原题:Secondary haematological dysplasia after CAR-T-cell therapy for acute lymphoblastic leukaemia in children.
共有 106 例患者因急性淋巴细胞白血病(ALL)接受了 CAR-T 治疗。
CAR-T在血液系统恶性肿瘤治疗中的应用日益广泛。成人患者接受CAR-T治疗后继发骨髓增生异常综合征(MDS)的病例已有报道。然而,目前尚无关于儿童急性淋巴细胞白血病(ALL)患者接受CAR-T后发生MDS风险的数据。我们研究了巴塞罗那圣胡安·德乌医院所有接受CAR-T治疗的儿童;对出现持续性血细胞减少者进行细胞学、细胞遗传学和分子水平评估,以筛查MDS。共有106例患者接受CAR-T治疗ALL。在40例CAR-T后未早期复发、也未接受后续治疗的患者中,有4例符合世界卫生组织骨髓增生异常标准。这4例患者在CAR-T前均接受过造血干细胞移植(HSCT),CAR-T后出现血细胞减少,并在骨髓中表现为严重发育异常。其中1例为宿主细胞来源、具有高危细胞遗传学特征的克隆性MDS,需要接受HSCT;另3例为供者细胞来源、未进展的发育异常。2例存活,处于完全缓解且血细胞减少稳定;1例死于ALL复发。据我们所知,这是首次报道儿童CAR-T治疗后MDS和血液细胞发育异常,提示需对CAR-T后持续血细胞减少的儿童进行监测。
The use of CAR-T is becoming more widespread in the treatment of haematological malignancies. In adults, secondary myelodysplastic syndromes (MDS) after CAR-T have been described. However, there are currently no data on the risk of MDS following CAR-T in children treated for acute lymphoblastic leukaemia (ALL). We studied all children treated with CAR-T cells at Hospital Sant Joan de D u in Barcelona and those with persistent cytopenias were evaluated at the cytological, cytogenetic, and molecular levels to look for MDS. A total of 106 patients received CAR-T for ALL. Among 40 patients without early relapse or subsequent therapy after CAR-T, four fulfilled the WHO criteria for myelodysplasia. These four patients had received a haematopoietic stem cell transplantation (HSCT) prior to CAR-T and presented cytopenias with severe dysplastic changes in bone marrow after CAR-T. One patient had clonal MDS with high-risk cytogenetics arising from the host cells requiring a HSCT. Three patients had non-progressive dysplasia arising from the donor cells. Two are alive in complete remission with stable cytopenias and one succumbed to ALL relapse. This is the first description of post-CAR-T MDS and haematological dysplasia in children and highlights the need to monitor children with persistent post-CAR-T cytopenias.
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