Rytting Michael E, Jabbour Elias J, Jorgensen Jeffrey L, Ravandi Farhad, Franklin Anna R, Kadia Tapan M, Pemmaraju Naveen, Daver Naval G, Ferrajoli Alessandra, Garcia-Manero Guillermo, Konopleva Marina Y, Borthakur Gautam, Garris Rebecca, Wang Sa, Pierce Sherry, Schroeder Kurt, Kornblau Steven M, Thomas Deborah A, Cortes Jorge E, O'Brien Susan M, Kantarjian Hagop M
Pediatrics-Patient Care, the University of Texas MD Anderson Cancer Center, Texas.
Department of Leukemia, the University of Texas MD Anderson Cancer Center, Texas.
Am J Hematol. 2016 Aug;91(8):819-23. doi: 10.1002/ajh.24419. Epub 2016 Jun 30.
Several studies reported improved outcomes of adolescents and young adults (AYA) with acute lymphoblastic leukemia (ALL) treated with pediatric-based ALL regimens. This prompted the prospective investigation of a pediatric Augmented Berlin-Frankfurt-Münster (ABFM) regimen, and its comparison with hyper-fractionated cyclophosphamide, vincristine, Adriamycin, and dexamethasone (hyper-CVAD) in AYA patients. One hundred and six AYA patients (median age 22 years) with Philadelphia chromosome- (Ph) negative ALL received ABFM from October 2006 through March 2014. Their outcome was compared to 102 AYA patients (median age 27 years), treated with hyper-CVAD at our institution. The complete remission (CR) rate was 93% with ABFM and 98% with hyper-CVAD. The 5-year complete remission duration (CRD) were 53 and 55%, respectively (P = 0.98). The 5-year overall survival (OS) rates were 60 and 60%, respectively. The MRD status on Day 29 and Day 84 of therapy was predictive of long-term outcomes on both ABFM and hyper-CVAD. Severe regimen toxicities with ABFM included hepatotoxicity in 41%, pancreatitis in 11%, osteonecrosis in 9%, and thrombosis in 19%. Myelosuppression-associated complications were most significant with hyper-CVAD. In summary, ABFM and hyper-CVAD resulted in similar efficacy outcomes, but were associated with different toxicity profiles, asparaginase-related with ABFM and myelosuppression-related with hyper-CVAD. Am. J. Hematol. 91:819-823, 2016. © 2016 Wiley Periodicals, Inc.
多项研究报告称,采用基于儿科的急性淋巴细胞白血病(ALL)治疗方案治疗的青少年及年轻成人(AYA)患者预后得到改善。这促使人们对儿科强化柏林-法兰克福-明斯特(ABFM)方案进行前瞻性研究,并将其与AYA患者的超分割环磷酰胺、长春新碱、阿霉素和地塞米松(hyper-CVAD)方案进行比较。2006年10月至2014年3月期间,106例费城染色体阴性(Ph-)的AYA ALL患者接受了ABFM方案治疗。将他们的预后与在本机构接受hyper-CVAD方案治疗的102例AYA患者(中位年龄27岁)进行比较。ABFM方案的完全缓解(CR)率为93%,hyper-CVAD方案为98%。5年完全缓解持续时间(CRD)分别为53%和55%(P = 0.98)。5年总生存率(OS)分别为60%和60%。治疗第29天和第84天的微小残留病(MRD)状态可预测ABFM和hyper-CVAD方案的长期预后。ABFM方案的严重治疗毒性包括41%的肝毒性、11%的胰腺炎、9%的骨坏死和19%的血栓形成。hyper-CVAD方案与骨髓抑制相关的并发症最为显著。总之,ABFM和hyper-CVAD方案疗效相似,但毒性特征不同,ABFM方案与天冬酰胺酶相关,hyper-CVAD方案与骨髓抑制相关。《美国血液学杂志》91:819 - 823,2016年。© 2016威利期刊公司