Treatment of therapy-related myeloid neoplasms with high-dose cytarabine/mitoxantrone followed by hematopoietic stem cell transplant

被引:20
作者
Godley, Lucy A. [1 ,2 ]
Njiaju, Uchenna O. [1 ]
Green, Margaret [1 ]
Weiner, Howard [1 ]
Lin, Shang [3 ]
Odenike, Olatoyosi [1 ,2 ]
Rich, Elizabeth S. [1 ,2 ]
Artz, Andrew [1 ,2 ]
Van Besien, Koen [1 ,2 ]
Daugherty, Christopher K. [1 ,2 ]
Zhang, Yanming [1 ,2 ]
Le Beau, Michelle M. [1 ,2 ]
Stock, Wendy [1 ,2 ]
Larson, Richard A. [1 ,2 ]
机构
[1] Univ Chicago, Hematol Oncol Sect, Dept Med, Chicago, IL 60637 USA
[2] Univ Chicago, Canc Res Ctr, Chicago, IL 60637 USA
[3] Univ Chicago, Dept Hlth Studies, Chicago, IL 60637 USA
关键词
Therapy-related myeloid neoplasm; high-dose cytarabine; mitoxantrone; ACUTE MYELOGENOUS LEUKEMIA; BALANCED CHROMOSOME-ABNORMALITIES; BONE-MARROW-TRANSPLANTATION; MYELODYSPLASTIC SYNDROMES; LONG-TERM; INDUCTION; CYTARABINE; MITOXANTRONE; TRIALS; ADULTS;
D O I
10.3109/10428191003763468
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Few clinical protocols have focused on patients with therapy-related myeloid neoplasms (t-MN). Therefore, we enrolled 32 patients with previously untreated t-MN on a clinical trial testing the effectiveness of a unified induction regimen of high-dose cytarabine and mitoxantrone. The complete remission (CR) rate was 66% (95% CI 47-81%) and the partial remission (PR) rate was 16% (95% CI 5-33%), for an overall response rate of 82%. Day 30 treatment mortality was 9% (3/32), and the most serious induction toxicity was cardiac dysfunction. Among the patients with CR, 13 (62%) received consolidation therapy using an allogeneic hematopoietic cell transplant (HCT), four (21%) received an autologous HCT, and three (16%) received further chemotherapy. We observed long-term disease-free survival in patients who received all three types of consolidation therapy. The remission induction of high-dose cytarabine and mitoxantrone for t-MN is a well-tolerated efficacious combination, which allows aggressive consolidation and long-term disease-free survival.
引用
收藏
页码:995 / 1006
页数:12
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