Clinical outcomes of decitabine treatment for myelodysplastic syndrome patinents at the national insitute of hematology and blood transfusion

Nguyễn Quang Hảo, Trần Tuấn Anh, Lưu Thị Thu Hương, Vũ Minh Phương, Vũ Đức Bình, Nguyễn Ngọc Dũng, Nguyễn Hà Thanh, Bạch Quốc Khánh, Dương Quốc Chính

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Abstract

This study was conducted to evaluation of clinical outcomes of decitabine treatment for MDS patients. 43 MDS patients (according to WHO 2016) have been diagnosed and treated at the National Institute of Hematology and Blood Transfusion, Hanoi, Vietnam. Patients were grouped based on their risk level according to IPSSR standard and were singly treated with decitabine. Results showed that 43 patients treated with decitabine achieved a significantly high overall response rate of 60.5%, including 41.9% achieving complete responses and 18.6% partial responses. Median time progression to acute myelogenous leukemia stage was 21.8 months. The most common adverse effects included myelosuppression (neutropenia 27.9%, anemia 18.6% and thrombocytopenia 41.9%), constipation 32.6%, vomiting 27.9%, cough 23.3%, fever 18.6%, diarrhea 16.3%, and pneumonia 16.3%. Decitabine was found to be clinically effective in the treatment of patients in both lower - risk group and higher - risk group MDS, with proven durable responses.

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References

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