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加拿大婴儿急性淋巴细胞白血病(ALL)、亚二倍体ALL及混合表型急性白血病(MPAL)的预后因素与结局:CYP-C的报告

Prognostic factors and outcomes of infant acute lymphoblastic leukemia (ALL), hypodiploid ALL, and mixed-phenotype acute leukemia (MPAL) in Canada: a report from CYP-C.

作者信息

Tibout Pauline, Ledjiar Omar, Athale Uma, Rayar Meera, Kulkarni Ketan, Truong Tony, Cellot Sonia, Bittencourt Henrique, Pelland-Marcotte Marie-Claude, Tran Thai Hoa

机构信息

Division of Pediatric Hematology-Oncology, Charles-Bruneau Cancer Center, CHU Sainte-Justine, University of Montreal, Montreal, Canada.

Unité de recherche clinique appliquée, Research Centre, CHU Sainte-Justine, Montreal, Canada.

出版信息

Leuk Lymphoma. 2022 Dec;63(13):3208-3216. doi: 10.1080/10428194.2022.2118536. Epub 2022 Sep 6.

DOI:10.1080/10428194.2022.2118536
PMID:36067507
Abstract

The epidemiology of infant acute lymphoblastic leukemia (ALL), hypodiploid ALL, and mixed-phenotype acute leukemia (MPAL) in Canada is unknown. The main objective was to describe the prevalence, prognostic factors, and outcomes of three rare and high-risk ALL subtypes in Canada. This is a retrospective study using the Cancer in Young People-Canada (CYP-C) database. Event-free survival (EFS) and overall survival (OS) were described by the Kaplan-Meier method and compared using the log-rank test. Among 2626 children aged 0-14 years diagnosed with B-cell acute lymphoblastic leukemia (B-ALL) between 2001 and 2018, 227 (8.6%) patients were identified to be infant ALL ( = 139), hypodiploid ALL ( = 43), or MPAL ( = 45). The 5-year EFS/OS was significantly worse in the infant ALL subgroup compared to that of hypodiploid ALL and MPAL. For the entire cohort, presenting White blood cells (WBCs) ≥50 × 10/L was independently associated with worse EFS/OS.

摘要

加拿大婴儿急性淋巴细胞白血病(ALL)、亚二倍体ALL和混合表型急性白血病(MPAL)的流行病学情况尚不清楚。主要目的是描述加拿大三种罕见且高危的ALL亚型的患病率、预后因素和结局。这是一项使用加拿大青少年癌症(CYP-C)数据库的回顾性研究。采用Kaplan-Meier方法描述无事件生存期(EFS)和总生存期(OS),并使用对数秩检验进行比较。在2001年至2018年间确诊为B细胞急性淋巴细胞白血病(B-ALL)的2626名0至14岁儿童中,有227名(8.6%)患者被确定为婴儿ALL(n = 139)、亚二倍体ALL(n = 43)或MPAL(n = 45)。与亚二倍体ALL和MPAL相比,婴儿ALL亚组的5年EFS/OS明显更差。对于整个队列,初诊时白细胞(WBC)≥50×10⁹/L与较差的EFS/OS独立相关。

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