Abstract |
Myelodysplastic syndromes (MDS) are heterogeneous diseases. Patients with blast counts of more than 20% of nucleated bone marrow cells have a high risk of short survival. We treated six patients with refractory anemia with excess of blast in transformation (RAEBiT) with low dose cytosine arabinoside (LD Ara-C). We had one partial remission (PR), surviving 16 weeks and two complete remissions (CR), surviving 22 and 55+ months. Myelosuppression was dominant in all patients, but was not as serious as with conventional remission-induction treatments for leukemias. Bone marrow aplasia occurred in all responding patients, but a differentiation effect is possible too. Maintenance therapy with LD Ara-C may be important for the two long-lasting CR.
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Authors | M A Fridrik, G Wahl, W Herbinger |
Journal | Blut
(Blut)
Vol. 57
Issue 6
Pg. 357-60
(Dec 1988)
ISSN: 0006-5242 [Print] Germany |
PMID | 3207893
(Publication Type: Journal Article)
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Chemical References |
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Topics |
- Adult
- Aged
- Anemia, Refractory, with Excess of Blasts
(complications, drug therapy, pathology)
- Bacterial Infections
(etiology)
- Bone Marrow
(drug effects)
- Cell Transformation, Neoplastic
(drug effects, pathology)
- Cytarabine
(administration & dosage, adverse effects)
- Drug Administration Schedule
- Female
- Hematopoietic Stem Cells
(drug effects, pathology)
- Humans
- Male
- Middle Aged
- Remission Induction
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