Salzer Wanda L, Devidas Meenakshi, Shuster Jonathan J, Wang Chenguang, Chauvenet Allen, Asselin Barbara L, Camitta Bruce M, Kurtzberg Joanne
Keesler Medical Center, Keesler AFB, Biloxi, MS, USA.
J Pediatr Hematol Oncol. 2007 Jun;29(6):369-75. doi: 10.1097/MPH.0b013e3180640d54.
The Pediatric Oncology Group 9203 pilot protocol was designed to determine the feasibility of delivering 29 biweekly doses of polyethylene glycol (PEG)-L-asparaginase, on a backbone of intensive multiagent antimetabolite-based consolidation and maintenance in higher risk B-precursor acute lymphoblastic leukemia. Between June 1992 and August 1993, 34 patients were enrolled on this limited institution pilot. The 5-year event-free survival (+/-standard error) and overall survival (+/-standard error) were 68+/-8% and 76+/-7%, respectively. Excessive toxicities attributed to PEG-L-asparaginase and myelosuppression associated with cytosine arabinoside were encountered during consolidation resulting in early study closure and modification of therapy for those already enrolled. Ninety-two percent of methotrexate/cytosine arabinoside cycles were associated with grades 3 to 4 myelosuppression, and 24% resulted in delays in therapy of more than 7 days. Fifteen PEG-L-asparaginase related toxicities occurred in 13 patients (8 allergy, 4 pancreas, 2 central nervous system, and 1 hemorrhage). Intensification of therapy with PEG-L-asparaginase resulted in event-free survival and overall survival comparable to other studies of the same time period without the use of agents associated with long-term complications, such as anthracyclines, epipodophyllotoxins, and alkylating agents. However, excessive toxicity occurred with intensified PEG-L-asparaginase and antimetabolite based therapy delivered on this schedule.
儿童肿瘤学组9203试验方案旨在确定在高风险B前体急性淋巴细胞白血病患者中,以强化多药抗代谢物为基础的巩固和维持治疗方案为框架,给予29剂每两周一次的聚乙二醇(PEG)-L-天冬酰胺酶的可行性。1992年6月至1993年8月期间,34例患者入组了这个机构有限的试验。5年无事件生存率(±标准误差)和总生存率(±标准误差)分别为68±8%和76±7%。在巩固治疗期间,出现了归因于PEG-L-天冬酰胺酶的过度毒性以及与阿糖胞苷相关的骨髓抑制,导致研究提前结束,并对已入组患者的治疗方案进行了修改。92%的甲氨蝶呤/阿糖胞苷疗程与3至4级骨髓抑制相关,24%导致治疗延迟超过7天。13例患者出现了15次与PEG-L-天冬酰胺酶相关的毒性反应(8例过敏、4例胰腺毒性、2例中枢神经系统毒性和1例出血)。与同期其他未使用与长期并发症相关药物(如蒽环类药物、鬼臼毒素和烷化剂)的研究相比,使用PEG-L-天冬酰胺酶强化治疗后的无事件生存率和总生存率相当。然而,按照这个方案给予强化的PEG-L-天冬酰胺酶和基于抗代谢物的治疗会出现过度毒性。