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논문 기본 정보

자료유형
학술저널
저자정보
Fatma Arikan (Department of Hematology Marmara University Hospital Istanbul Turkey) Tayfur Toptas (Department of Hematology, Marmara University Hospital, Istanbul, Turkey) Isik Kaygusuz Atagunduz (Department of Hematology Marmara University Hospital Istanbul Turkey) Tarik Ercan (Department of Hematology Marmara University Hospital Istanbul Turkey) Ozen Oruc (Department of Hematology Marmara University Hospital Istanbul Turkey) Fergun Yilmaz (Department of Hematology Marmara University Hospital Istanbul Turkey) Tulin Tuglular (Department of Hematology Marmara University Hospital Istanbul Turkey)
저널정보
대한혈액학회 Blood Research Blood Research Vol.56 No.4
발행연도
2021.12
수록면
322 - 331 (10page)
DOI
10.5045/br.2021.2021101

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Background In this retrospective cohort of patients with primary, post-polycythemia vera, or post-essential thrombocythemia myelofibrosis, 57 patients with MF who received ruxolitinib for MF-related symptoms or symptomatic splenomegaly were evaluated. Methods The median age of the patients in this cohort was approximately 58 years. Of these, there were 33 patients (57.9%) in INT-1, 23 patients (40.4%) in INT-2, and 1 patient (1.8%) at high risk. Overall, spleen size reduction of at least 35% (spleen response) was achieved in 56.6% and 63.3% of all cohort and INT-1 risk at any time, respectively. Results Symptom response and clinical improvement were observed in 21.7% and 60.7% of patients, respectively. Anemia and thrombocytopenia were prevalent, but manageable. About 73.7% of patients continued treatment during a median follow-up of 22 months. Two-year OS probability was approximately 84.5% (95% CI, 63.1?94.0%) and 62.3% (95% CI, 37.5?79.6%) for the intermediate-1 and -2 risk groups, respectively. Conclusion Real-life experience in a community-based hospital confirms the efficacy and safety profile of ruxolitinib in intermediate-risk myelofibrosis. Treatment discontinuation rates were lower than those in clinical trials.

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