Department of Hematology/Oncology, Shanghai Children's Medical Center, Shanghai Jiao Tong University School of Medicine, Key Laboratory of Pediatric Hematology & Oncology of China Ministry of Health, and National Children's Medical Center, Shanghai, China.
Department of Pediatric, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Int J Cancer. 2021 Jul 1;149(1):158-168. doi: 10.1002/ijc.33529. Epub 2021 Mar 26.
Asparaginase (Asp) is one of the most important drugs for treating acute lymphoblastic leukemia (ALL). However, off-protocol Asp administration (OPAA) or hypersensitivity may disturb its pharmacokinetic profile. In this retrospective study, we sought to determine whether OPAA and hypersensitivity to Escherichia coli asparaginase (E coli Asp) impaired extramedullary relapse prevention in a pediatric ALL cohort treated according to SCMC-ALL-2005 protocol from 2005 to 2014 at the Shanghai Children's Medical Center (SCMC). In total, 676 patients were enrolled in this study, including 369 with OPAA and 60 exhibiting hypersensitivity to E coli Asp. At the end of the most recent follow-up, 58 patients had extramedullary relapse. The 5-year cumulative extramedullary relapse incidence in patients with OPAA was 11.01%, whereas that in patients without OPAA was 5.28% (P = .0036). Moreover, the 5-year cumulative extramedullary relapse incidence in patients that exhibited hypersensitivity to E coli Asp was 16.48%, whereas that in patients without hypersensitivity was 7.59% (P = .0195). Concerning the relapse site, OPAA not only increased central nervous system (CNS) relapse but testicular relapse as well. Based on Fine and Gray multivariate analysis, OPAA and hypersensitivity to Asp were independent risk factors for extramedullary relapse. In conclusion, to prevent extramedullary relapse of ALL, adequate duration to administrate Asp was more important than the total dosage, and more attention should be paid to Asp inadequate due to hypersensitivity.
天冬酰胺酶(Asp)是治疗急性淋巴细胞白血病(ALL)的最重要药物之一。然而,不合规的 Asp 给药(OPAA)或过敏可能会干扰其药代动力学特征。在这项回顾性研究中,我们试图确定在上海儿童医学中心(SCMC)根据 SCMC-ALL-2005 方案治疗的小儿 ALL 队列中,OPAA 和对大肠埃希菌天冬酰胺酶(E coli Asp)的过敏是否会损害髓外复发预防。共有 676 名患者入组本研究,其中 369 名患者有 OPAA,60 名患者对 E coli Asp 过敏。在最近一次随访结束时,58 名患者发生髓外复发。OPAA 患者的 5 年累积髓外复发率为 11.01%,而无 OPAA 的患者为 5.28%(P =.0036)。此外,对 E coli Asp 过敏的患者的 5 年累积髓外复发率为 16.48%,而无过敏的患者为 7.59%(P =.0195)。就复发部位而言,OPAA 不仅增加了中枢神经系统(CNS)的复发,还增加了睾丸的复发。基于 Fine 和 Gray 多变量分析,OPAA 和对 Asp 的过敏是髓外复发的独立危险因素。总之,为了预防 ALL 的髓外复发,足够的 Asp 给药时间比总剂量更重要,应更加注意因过敏导致的 Asp 不足。