Fathi Amir T, DeAngelo Daniel J, Stevenson Kristen E, Kolitz Jonathan E, Asch Julie D, Amrein Philip C, Attar Eyal C, Steensma David P, Wadleigh Martha, Foster Julia, Connolly Christine, Galinsky Ilene, Devoe Craig E, Stone Richard M, Neuberg Donna S, Ballen Karen K
Massachusetts General Hospital Cancer Center, Boston, Massachusetts.
Dana-Farber Cancer Institute, Boston, Massachusetts.
Cancer. 2016 Aug 1;122(15):2379-88. doi: 10.1002/cncr.30037. Epub 2016 May 12.
Outcomes among older patients with acute lymphoblastic leukemia remain poor. This study sought to determine the efficacy of an intensified, multi-agent approach derived from a Dana-Farber consortium trial in younger adults for patients older than 50 years (trial identifier NCT00973752).
The primary endpoint was overall survival (OS) at 1 year. Patients received induction chemotherapy with vincristine, prednisone, doxorubicin, and pegylated asparaginase. Imatinib was incorporated for Philadelphia chromosome-positive disease. After induction, the first consolidation incorporated clofarabine. Patients in remission could proceed to allogeneic hematopoietic cell transplantation (HCT) after induction and consolidation I. Those not receiving HCT went on to receive central nervous system, consolidation II, and continuation phases of treatment.
Thirty patients were enrolled: 19 achieved a complete remission (CR) after induction and 1 achieved CR after consolidation I for a CR rate of 67%. Sixteen patients underwent HCT. The proportion surviving at 1 year was 63%, and this met the primary endpoint. The 2-year OS rate was 52% (n = 30), and the 2-year disease-free survival rate was 52% for patients achieving CR (n = 20). There was no survival advantage among those undergoing HCT. Therapy-related hyperbilirubinemia prompted adjustments and limitations to asparaginase dosing.
Intensified chemotherapy can result in improved outcomes in comparison with historical data. Additional studies of similarly intensive regimens are warranted in this population. Cancer 2016;122:2379-2388. © 2016 American Cancer Society.
老年急性淋巴细胞白血病患者的预后仍然很差。本研究旨在确定一种强化的多药联合方案的疗效,该方案源自达纳-法伯癌症联盟针对年轻成年人的一项试验,用于50岁以上的患者(试验标识符NCT00973752)。
主要终点为1年总生存期(OS)。患者接受长春新碱、泼尼松、阿霉素和聚乙二醇化天冬酰胺酶的诱导化疗。对于费城染色体阳性疾病,加入伊马替尼。诱导后,首次巩固治疗采用氯法拉滨。缓解的患者在诱导和巩固I后可进行异基因造血细胞移植(HCT)。未接受HCT的患者继续接受中枢神经系统治疗、巩固II和后续治疗阶段。
共纳入30例患者:19例在诱导后达到完全缓解(CR),1例在巩固I后达到CR,CR率为67%。16例患者接受了HCT。1年生存率为63%,达到了主要终点。2年总生存率为52%(n = 30),达到CR的患者2年无病生存率为52%(n = 20)。接受HCT的患者没有生存优势。与治疗相关的高胆红素血症促使调整并限制了天冬酰胺酶的剂量。
与历史数据相比,强化化疗可改善预后。该人群有必要对类似的强化方案进行更多研究。《癌症》2016年;122:2379 - 2388。© 2016美国癌症协会。