Rinsho Ketsueki
Online ISSN : 1882-0824
Print ISSN : 0485-1439
ISSN-L : 0485-1439
Clinical Characterisitcs and Poor Outcomes in Patients with de novo AML with Trilineage Myelodysplasia
Kosei ARIMURAKazutaka KURIYAMAYasushi MIYAZAKIKazuhiro NAGAITakuya FUKUSHIMAShinichiro YOSHIDAYukiyoshi MORIUCHISaburo MOMITAMasao TOMONAGA
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1995 Volume 36 Issue 2 Pages 98-105

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Abstract

De novo AML with trilineage myelodysplasia (AML/TMDS) is reported to account for 10∼15% of de novo AML and respond poorly to conventional intensive chemotherapy, In our series, 12 (25%) of 48 patients with de novo AML were diagnosed as AML/TMDS. We found that the platelet count was significantly higher (p<0.05), and the blast percentage of the bone marrow was significantly lower (p<0.05) in the AML/TMDS group than in the AML/non-TMDS group. Sex ratio, age, WBC and RBC count did not significantly differ between the two groups. The immunological markers and the myeloperoxidase positivity of the blasts of AML/TMDS varied widely. The CR rate was 66.7% in the AML/TMDS group and 83.3% in the AML/non-TMDS group. Dysplastic changes were still detected in the bone marrow smears in 7 of 8 AML/TMDS cases who achieved complete remission. The AML/TMDS group showed significantly shorter CR duration (median; 169 days) and survival (median; 511 days, p<0.05). However, in two cases which underwent allogeneic bone marrow transplantaion (allo-BMT) during early relapse phase the disease-free survival has extended over 4 years and 2 years 8 months, respectively. Thus, we would like to propose that allo-BMT should be performed as early as possible to overcome poor outcome of AML/TMDS.

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© 1995 The Japanese Society of Hematology
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