Department of Pediatrics, Okayama University Hospital, Okayama, Japan.
Department of Pediatrics, Kyoto Prefectural University of Medicine, Graduate School of Medical Science, Kyoto, Japan.
Br J Haematol. 2023 Jun;201(6):1200-1208. doi: 10.1111/bjh.18745. Epub 2023 Mar 9.
Asparaginase is an essential drug for acute lymphoblastic leukaemia (ALL) treatment, but has several side effects, and its discontinuation often compromises patient outcomes. In the prospective Japan Association of Childhood Leukaemia Study ALL-02 protocol, two major changes were made: (1) additional chemotherapies to compensate for the reduction of treatment intensity when asparaginase was discontinued and (2) more intensive concomitant corticosteroid administration, relative to our previous ALL-97 protocol. In ALL-02 study, 1192 patients were included and L-asparaginase was discontinued for 88 (7.4%). Discontinuation due to allergy was markedly decreased relative to the ALL-97 protocol (2.3% vs 15.4%). Event-free survival (EFS) among patients with T-ALL was compromised when L-asparaginase was discontinued, as well as among patients with high-risk B-cell ALL, especially when discontinued before maintenance therapy. Moreover, multivariate analysis identified discontinuation of L-asparaginase as an independent poor prognostic factor for EFS. In the current study, additional chemotherapies failed to fully compensate for L-asparaginase discontinuation, illustrating the difficulty of replacing asparaginase with other classes of drugs, although this study was not designed to evaluate the effect of these modifications. Concomitant intensive corticosteroid treatment may help to reduce allergy to asparaginase. These results will assist in further optimization of asparaginase use.
门冬酰胺酶是治疗急性淋巴细胞白血病(ALL)的重要药物,但具有多种副作用,其停药常常会影响患者的预后。在前瞻性日本儿童白血病研究协会 ALL-02 方案中,进行了两项重大改变:(1)当门冬酰胺酶停药时,增加了几种化疗药物以弥补治疗强度的降低;(2)与我们之前的 ALL-97 方案相比,增加了更强化的伴随皮质激素治疗。在 ALL-02 研究中,共纳入 1192 例患者,其中 88 例(7.4%)停用了 L-门冬酰胺酶。与 ALL-97 方案相比,由于过敏而停药的比例明显降低(2.3% vs 15.4%)。L-门冬酰胺酶停药会影响 T-ALL 患者的无事件生存(EFS),也会影响高危 B 细胞 ALL 患者的 EFS,尤其是在维持治疗前停药的患者。此外,多变量分析确定 L-门冬酰胺酶的停药是 EFS 的独立不良预后因素。在本研究中,增加的化疗药物未能完全弥补 L-门冬酰胺酶的停药,这表明用其他类别的药物替代门冬酰胺酶具有一定难度,尽管该研究并非旨在评估这些修改的效果。同时强化皮质激素治疗可能有助于减少门冬酰胺酶过敏。这些结果将有助于进一步优化门冬酰胺酶的使用。