Bender Cynthia, Maese Luke, Carter-Febres Maria, Verma Anupam
Department of Pharmacy, Primary Children's Hospital, Salt Lake City, UT, USA.
Division of Hematology/Oncology, Department of Pediatrics, University of Utah and Primary Children's Hospital, Salt Lake City, UT, USA.
Blood Lymphat Cancer. 2021 Apr 19;11:25-40. doi: 10.2147/BLCTT.S245210. eCollection 2021.
Acute lymphoblastic leukemia (ALL) is a heterogenous hematological malignancy representing 25% of all cancers in children less than 15 years of age. Significant improvements in survival and cure rates have been made over the past four decades in pediatric ALL treatment. Asparaginases, derived from and , have become a critical component of ALL therapy since the 1960s. Asparaginases cause depletion of serum asparagine, leading to deprivation of this critical amino acid for protein synthesis, and hence limit survival of lymphoblasts. Pegaspargase, a conjugate of monomethoxypolyethylene glycol (mPEG) and L-asparaginase, has become an integral component of pediatric upfront and relapsed ALL protocols due to its longer half-life and improved immunogenicity profile compared to native asparaginase preparations. Over the past two decades great strides have been made in outcomes for pediatric ALL due to risk stratification, incorporation of multiagent chemotherapy protocols, and central nervous system prophylaxis with pegaspargase having played an important role in this success. However, adolescents and young adults (AYA) with ALL when treated on contemporaneous trials using adult ALL regimens, continue to have poor outcomes. There is increasing realization of adapting pediatric trial regimens for treating AYAs, especially those incorporating higher intensity of chemotherapeutic agents with pegaspargase being one such agent. Dose or treatment-limiting toxicity is observed in 25-30% of patients, most notable being hypersensitivity reactions. Other toxicities include asparaginase-associated pancreatitis, thrombosis, liver dysfunction, osteonecrosis, and dyslipidemia. Discontinuation or subtherapeutic levels of asparaginase are associated with inferior disease-free survival leading to higher risk of relapse, and in cases of relapse, a higher risk for remission failure. This article provides an overview of available evidence for use of pegaspargase in pediatric acute lymphoblastic leukemia.
急性淋巴细胞白血病(ALL)是一种异质性血液系统恶性肿瘤,占15岁以下儿童所有癌症的25%。在过去的四十年里,儿童ALL治疗的生存率和治愈率有了显著提高。自20世纪60年代以来,源自 和 的天冬酰胺酶已成为ALL治疗的关键组成部分。天冬酰胺酶会导致血清天冬酰胺减少,从而使蛋白质合成缺乏这种关键氨基酸,进而限制淋巴母细胞的存活。培门冬酶是单甲氧基聚乙二醇(mPEG)与L-天冬酰胺酶的缀合物,由于其半衰期更长且免疫原性优于天然天冬酰胺酶制剂,已成为儿童初治和复发ALL方案的重要组成部分。在过去的二十年里,由于风险分层、多药化疗方案的纳入以及培门冬酶用于中枢神经系统预防在这一成功中发挥了重要作用,儿童ALL的治疗结果取得了巨大进展。然而,青少年和青年成人(AYA)ALL患者在使用成人ALL方案进行同期试验治疗时,预后仍然较差。越来越意识到需要调整儿童试验方案来治疗AYA患者,特别是那些采用更高强度化疗药物的方案,培门冬酶就是这样一种药物。25%-30%的患者会出现剂量或治疗限制性毒性,最常见的是过敏反应。其他毒性包括天冬酰胺酶相关的胰腺炎、血栓形成、肝功能障碍、骨坏死和血脂异常。天冬酰胺酶的停用或低于治疗水平与无病生存率降低相关,导致复发风险增加,并且在复发情况下,缓解失败的风险更高。本文概述了培门冬酶在儿童急性淋巴细胞白血病中应用的现有证据。