首页> 外文OA文献 >Sequential administration of gemtuzumab ozogamicin and conventional chemotherapy as first line therapy in elderly patients with acute myeloid leukemia: a phase II study (AML-15) of the EORTC and GIMEMA leukemia groups.
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Sequential administration of gemtuzumab ozogamicin and conventional chemotherapy as first line therapy in elderly patients with acute myeloid leukemia: a phase II study (AML-15) of the EORTC and GIMEMA leukemia groups.

机译:老年急性急性髓细胞性白血病的老年患者顺序应用吉妥单抗ozogamicin和常规化疗作为一线治疗:EORTC和GIMEMA白血病组的II期研究(AML-15)。

摘要

BACKGROUND AND OBJECTIVES: Acute myeloid leukemia (AML) in the elderly is associated with low rates of response to conventional chemotherapy and long-term survival, highlighting the need for innovative treatment strategies. Gemtuzumab ozogamicin (GO) is an immunoconjugate that has shown activity in relapsed AML with a favorable safety profile. The aim of this collaborative trial was to assess the feasibility, safety, and antileukemic activity of administering GO followed by conventional chemotherapy as first line therapy in patients aged 61-75 years with AML. DESIGN AND METHODS: Eligible patients received frontline treatment with GO 9 mg/m2 infused intravenously on days 1 and 15. Following response assessment to GO, patients were started on conventional chemotherapy consisting of the MICE regimen (mitoxantrone, cytarabine, etoposide). No further treatment was planned for complete responders. RESULTS: Among the 57 evaluable patients, 38 (67%) completed the entire sequential treatment as planned. The overall response rate to the entire induction sequence was 54.4% (31/57), with complete remission (CR) in 35.1% and complete remission with incomplete platelet recovery (CRp) in 19.3%. Rates of failure due to treatment-related mortality or resistant disease were 14.1% (3 toxic deaths during the GO segment, 5 during MICE) and 29.9%, respectively. An initial response to GO was documented in 20 patients (35.1%), with CR in 22.8% and CRp in 12.3%; 6 additional patients entered a partial remission. Reversible myelosuppression and liver toxicity were the main adverse events during both segments of induction. Frontline GO was associated with modest mucosal and gastrointestinal toxicity, but grade 3-4 pancytopenia was universal and prolonged. Hepatic veno-occlusive disease developed in 3 patients after GO and 2 after MICE, resulting in 4 deaths from liver failure. One-year survival at follow-up was 34%. Twelve patients continue in CR/CRp after a median of 226 days. INTERPRETATION AND CONCLUSIONS: The sequential combination of GO and conventional chemotherapy is a feasible and active treatment strategy for older patients with untreated AML. This novel regimen is now being compared in a phase III trial (AML-17).
机译:背景与目的:老年人的急性髓细胞性白血病(AML)与常规化疗反应率低和长期生存相关,这突出了对创新治疗策略的需求。 Gemtuzumab ozogamicin(GO)是一种免疫偶联物,在复发性AML中显示出活性,并具有良好的安全性。这项合作试验的目的是评估在61-75岁的AML患者中,先行行GO化疗后再行常规化学疗法作为一线治疗的可行性,安全性和抗白血病活性。设计与方法:符合条件的患者在第1天和第15天接受一线GO 9 mg / m2静脉输注的一线治疗。对GO的反应评估后,患者开始接受由MICE方案(米托蒽醌,阿糖胞苷,依托泊苷)组成的常规化疗。完全缓解者未计划进一步治疗。结果:在57位可评估患者中,有38位(67%)按计划完成了整个序贯治疗。整个诱导序列的总缓解率为54.4%(31/57),其中完全缓解(CR)为35.1%,完全缓解且血小板恢复不完全(CRp)为19.3%。由与治疗有关的死亡率或耐药性疾病导致的失败率分别为14.1%(GO期间3例中毒死亡,MICE期间5例中毒死亡)和29.9%。有20例患者(35.1%)记录了对GO的初始反应,其中CR占22.8%,CRp占12.3%。另外6名患者进入部分缓解。在诱导的两个阶段中,可逆的骨髓抑制和肝毒性是主要的不良事件。前线GO与适度的粘膜和胃肠道毒性有关,但3-4级全血细胞减少症普遍存在且持续时间较长。 GO术后3例发生肝静脉闭塞性疾病,MICE术后2例发生肝静脉闭塞性疾病,导致4例因肝衰竭死亡。随访一年生存率为34%。中位数226天后,有12名患者继续接受CR / CRp治疗。结论和结论:GO和常规化学疗法的序贯联合治疗是未治疗AML的老年患者的可行和积极的治疗策略。现在正在III期试验(AML-17)中比较这种新颖的治疗方案。

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