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氯雷他嗪(VNP40101M),一种新型的磺酰肼烷基化剂,用于60岁及以上先前未经治疗的急性髓性白血病患者。

Cloretazine (VNP40101M), a novel sulfonylhydrazine alkylating agent, in patients age 60 years or older with previously untreated acute myeloid leukemia.

作者信息

Giles Francis, Rizzieri David, Karp Judith, Vey Norbert, Ravandi Farhad, Faderl Stefan, Khan Khuda Dad, Verhoef Gregor, Wijermans Pierre, Advani Anjali, Roboz Gail, Kantarjian Hagop, Bilgrami Syed Fazl Ali, Ferrant Augustin, Daenen Simon M G J, Karsten Verena, Cahill Ann, Albitar Maher, Mufti Ghulam, O'Brien Susan

机构信息

The University of Texas M.D. Anderson Cancer Center, Department of Leukemia, Houston, TX 77030, USA.

出版信息

J Clin Oncol. 2007 Jan 1;25(1):25-31. doi: 10.1200/JCO.2006.07.0961. Epub 2006 Dec 4.

Abstract

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.

摘要

目的

氯雷他嗪(VNP40101M)是一种具有显著抗白血病活性的磺酰肼类烷化剂。对60岁及以上既往未治疗的急性髓系白血病(AML)或高危骨髓增生异常综合征(MDS)患者进行了一项氯雷他嗪的多中心II期研究。

患者与方法

氯雷他嗪600mg/m²作为单次静脉输注给药。患者按年龄、体能状态评分、细胞遗传学风险类别、AML类型和合并症进行分层。

结果

104例患者接受了研究治疗,中位年龄72岁(范围60至84岁)。31例患者(30%)的体能状态为2,且无患者具有良好的核型。根据造血细胞移植特异性合并症指数定义,47例患者(45%)有心脏病,25例患者(24%)有肝病,19例患者(18%)有肺病,均为研究入组时的情况。总缓解率为32%,29例患者(28%)达到完全缓解(CR),4例患者(4%)达到血小板未完全恢复的CR。44例初发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%。细胞遗传学风险类别为中等的56例患者的缓解率为39%,细胞遗传学风险不利的46例患者的缓解率为24%。19例(18%)患者在接受氯雷他嗪治疗后30天内死亡。中位总生存期为94天,1年生存率为14%;达到CR的患者中位生存时间为147天,1年生存率为28%。

结论

氯雷他嗪对老年AML或高危MDS患者具有显著活性且髓外毒性较小。尽管年龄和合并症增加,但缓解率仍保持一致。

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