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首页> 外文期刊>Journal of Clinical Oncology >Cloretazine (VNP40101M), a novel sulfonylhydrazine alkylating agent, in patients age 60 years or older with previously untreated acute myeloid leukemia.
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Cloretazine (VNP40101M), a novel sulfonylhydrazine alkylating agent, in patients age 60 years or older with previously untreated acute myeloid leukemia.

机译:氯雷他嗪(VNP40101M)是一种新型磺酰肼烷基化剂,适用于60岁或60岁以上先前未接受过治疗的急性髓性白血病的患者。

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PURPOSE: Cloretazine (VNP40101M) is a sulfonylhydrazine alkylating agent with significant antileukemia activity. A multicenter phase II study of cloretazine was conducted in patients 60 years of age or older with previously untreated acute myeloid leukemia (AML) or high-risk myelodysplastic syndrome (MDS). PATIENTS AND METHODS: Cloretazine 600 mg/m2 was administered as a single intravenous infusion. Patients were stratified by age, performance score, cytogenetic risk category, type of AML, and comorbidity. RESULTS: One hundred four patients, median age 72 years (range, 60 to 84 years), were treated on study. Performance status was 2 in 31 patients (30%) and no patient had a favorable karyotype. Forty-seven patients (45%) had cardiac disease, 25 patients (24%) had hepatic disease, and 19 patients (18%) had pulmonary disease, defined as per the Hematopoietic Cell Transplantation-Specific Comorbidity Index, at study entry. The overall response rate was 32%, with 29 patients (28%) achieving complete response (CR) and four patients (4%) achieving CR with incomplete platelet recovery. Response rates in 44 de novo AML patients, 45 secondary AML patients, and 15 high-risk MDS patients were 50%, 11%, and 40%, respectively. Response by cytogenetic risk category was 39% in 56 patients with intermediate cytogenetic risk and 24% in 46 patients with unfavorable cytogenetic risk. Nineteen (18%) patients died within 30 days of receiving cloretazine therapy. Median overall survival was 94 days, with a 1-year survival of 14%; the median duration of survival was 147 days, with a 1-year survival of 28% for those who achieved CR. CONCLUSION: Cloretazine has significant activity and modest extramedullary toxicity in elderly patients with AML or high-risk MDS. Response rates remain consistent despite increasing age and comorbidity.
机译:目的:氯雷他嗪(VNP40101M)是一种磺酰肼烷基化剂,具有显着的抗白血病活性。氯雷他嗪的多中心II期研究是在60岁或以上患有先前未经治疗的急性髓性白血病(AML)或高危骨髓增生异常综合征(MDS)的患者中进行的。患者和方法:氯雷他嗪600 mg / m2以单次静脉输注的方式给药。按年龄,表现评分,细胞遗传学风险类别,AML类型和合并症对患者进行分层。结果:研究治疗了104名患者,中位年龄为72岁(范围60至84岁)。 31名患者中有2名表现状态(30%),并且没有患者具有良好的核型。根据研究开始时的造血细胞特异性合并症指数定义,四十七名患者(45%)患有心脏病,二十五名患者(24%)患有肝病,而十九名患者(18%)患有肺部疾病。总体缓解率为32%,其中29例(28%)达到完全缓解(CR),四例(4%)达到CR而血小板恢复不完全。 44例从头治疗AML患者,45例继发性AML患者和15例高危MDS患者的缓解率分别为50%,11%和40%。按细胞遗传学风险类别分类的反应在中度细胞遗传学风险中的56例患者中为39%,在不良细胞遗传学风险中的46个患者中为24%。接受氯雷他嗪治疗的30天内有19名(18%)患者死亡。中位总生存期为94天,一年生存率为14%;中位生存期为147天,CR者的1年生存率为28%。结论:氯雷他嗪在老年AML或高危MDS患者中具有显着的活性和适度的髓外毒性。尽管年龄和合并症有所增加,但缓解率仍保持一致。

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