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. 2021 Feb 11;11(2):30.
doi: 10.1038/s41408-021-00424-4.

Refinement of prognosis and the effect of azacitidine in intermediate-risk myelodysplastic syndromes

Affiliations

Refinement of prognosis and the effect of azacitidine in intermediate-risk myelodysplastic syndromes

Konstantinos Liapis et al. Blood Cancer J. .
No abstract available

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Conflict of interest statement

I.K., N.A.V., A.S., E.H. and Vasiliki Pappa have received research funding from Celgene Corporation (of no relevance to this study). I.K., S.G.P., T.P.V., A.G.G., E.H., P.P., A.K., A.S., Vasiliki Pappa, and N.A.V. have received honoraria from Genesis Pharma Hellas S.A. (of no relevance to this study). All other authors have no conflicts of interest.

Figures

Fig. 1
Fig. 1. Kaplan–Meier analysis of survival outcomes in patients with intermediate-risk MDS.
(A) Kaplan–Meier curves of OS for patients with intermediate-risk MDS according to their IPSS-R value (3.5, 4.0, or 4.5). OS was better among patients with IPSS-R 3.5 as compared with IPSS-R > 3.5 (p = 0.039 by the log-rank test). (B) Kaplan-Meier curve of OS among patients with intermediate-risk MDS who received AZA (n = 166), as compared with patients who did not (n = 302). Median OS of the patients who received AZA (32.4 months [95% CI 25.2–39.6]) was similar to patients who did not receive AZA (29.0 months [23.9–34.1]); p = 0.291 by the log-rank test. (C) Kaplan-Meier curve of LFS among patients with intermediate-risk MDS who received AZA (n = 166), as compared with patients who did not (n = 302). Median LFS was 28.0 months (95% CI 19.0–37.0) for the AZA group and 26.0 months (21.8–30.2) for the non-AZA-treated group (p = 0.188). MDS myelodysplastic syndrome, OS overall survival, IPSS-R revised international prognostic scoring system, AZA azacitidine, LFS leukemia-free survival.

References

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