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Effectiveness of modified hyper‐CVAD chemotherapy regimen in the treatment of adult acute lymphoblastic leukemia: a retrospective experience

机译:改良的Hyper-CVAD化疗方案治疗成人急性淋巴细胞白血病的有效性:回顾性经验

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Several chemotherapy regimens have been developed for the treatment of acute lymphoblastic leukemia (ALL), but relapse still presents the most common obstacles to attaining long‐term survival. The hyper‐CVAD (hyperfractionated cyclophosphamide, vincristine, doxorubicin, and prednisolone)/HD MTX and Ara‐C (high‐dose methotrexate and cytarabine) chemotherapy regimen was first started in the MD Anderson Cancer Center as an intensive regimen for adult patients with ALL. The purpose of this study was to evaluate the effectiveness of a modified hyper‐CVAD protocol. We used hyper‐CVAD as consolidation/maintenance after remission induction with daunorubicin, vincristine, and prednisolone (and cyclophosphamide for T‐cell ALL only) rather than standard hyper‐CVAD in order to reduce treatment complications. This study was conducted as a retrospective review of medical records of ALL patients at 501 army hospital, Tehran, Iran, from 2005 to 2015. Three hundred and one patients underwent modified hyper‐CVAD chemotherapy regimen. Complete remission and overall survival (OS) rates were measured as primary endpoints. Two hundred and forty‐six (81.7%) reached complete remission (CR) during the first 6?months of treatment, and 55 patients (18.3%) did not reach CR. The 5‐year OS rate was 51.8% (95% CI (confidence interval): 45.1–57.8%). Modified hyper‐CVAD regimen is an efficient intensive chemotherapy regimen for consolidation/maintenance of adults with newly diagnosed ALL and has an acceptable 5‐year overall that is comparable to standard hyper‐CVAD regimen.
机译:已经开发出几种化学疗法来治疗急性淋巴细胞白血病(ALL),但是复发仍然是实现长期生存的最常见障碍。 hyper-CVAD(超分割环磷酰胺,长春新碱,阿霉素和泼尼松龙)/ HD MTX和Ara-C(大剂量甲氨蝶呤和阿糖胞苷)化疗方案最初在MD Anderson癌症中心开始,作为成人ALL患者的强化治疗方案。本研究的目的是评估改良的hyper-CVAD协议的有效性。为了减少治疗并发症,我们使用柔红霉素,长春新碱和泼尼松龙(仅对T细胞ALL使用环磷酰胺)诱导缓解后使用hyper-CVAD作为巩固/维持治疗,而不是标准的hyper-CVAD。这项研究是对2005年至2015年在伊朗德黑兰501军医院的ALL患者的病历进行的回顾性回顾。301位患者接受了改良的hyper-CVAD化疗方案。完全缓解和总体生存率是主要终点。在治疗的最初6个月中,有246例(81.7%)达到了完全缓解(CR),而55例(18.3%)没有达到CR。五年OS率为51.8%(95%CI(置信区间):45.1–57.8%)。改良的hyper-CVAD方案是一种有效的强化化疗方案,用于巩固/维持新诊断为ALL的成年人,其5年总体可接受水平与标准hyper-CVAD方案相当。

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