The effects of azacitidine on the response and prognosis of myelodysplastic syndrome and acute myeloid leukemia involving a bone marrow erythroblast frequency of >50
•HI could be achieved even if erythroblasts were dominant in BM.•The overall survival was also not inferior in erythroblast-predominant group.•Azacitidine could be an option irrespective of the numbers of erythroid cells in BM. We reviewed the cases of 68 consecutive patients who were diagnosed with...
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Published in | Leukemia Research Vol. 53; pp. 35 - 38 |
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Language | English |
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01.02.2017
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Abstract | •HI could be achieved even if erythroblasts were dominant in BM.•The overall survival was also not inferior in erythroblast-predominant group.•Azacitidine could be an option irrespective of the numbers of erythroid cells in BM.
We reviewed the cases of 68 consecutive patients who were diagnosed with myelodysplastic syndrome (MDS, n=61) or acute erythroleukemia (AEL, n=7) according to the World Health Organization (WHO) 2008 criteria and had previously been treated with azacitidine, a hypomethylating agent. Fifteen MDS patients had bone marrow erythroblast frequencies of ≥50%, and 6 out of the 7 AEL patients were reclassified as MDS (refractory anemia with excess blasts [RAEB]-1: 1, RAEB-2: 5) according to the revised WHO 2016 criteria. There was no difference between the overall response ratio (41%), as determined by a hematological improvement in at least one of 3 lineages, of these erythroid rich patients and that of the control group, which comprised 46 MDS patients with bone marrow erythroblast frequencies of <50%. Three MDS patients that exhibited erythroid predominance achieved complete remission. The overall survival period (median: 15 months) of the erythroblast-predominant group was not inferior to that of the control group (median: 16 months). These results indicate that azacitidine is a promising treatment option for MDS/AEL irrespective of the numbers of erythroid cells in the patient’s bone marrow. |
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AbstractList | Highlights • HI could be achieved even if erythroblasts were dominant in BM. • The overall survival was also not inferior in erythroblast-predominant group. • Azacitidine could be an option irrespective of the numbers of erythroid cells in BM. We reviewed the cases of 68 consecutive patients who were diagnosed with myelodysplastic syndrome (MDS, n=61) or acute erythroleukemia (AEL, n=7) according to the World Health Organization (WHO) 2008 criteria and had previously been treated with azacitidine, a hypomethylating agent. Fifteen MDS patients had bone marrow erythroblast frequencies of ≥50%, and 6 out of the 7 AEL patients were reclassified as MDS (refractory anemia with excess blasts [RAEB]-1: 1, RAEB-2: 5) according to the revised WHO 2016 criteria. There was no difference between the overall response ratio (41%), as determined by a hematological improvement in at least one of 3 lineages, of these erythroid rich patients and that of the control group, which comprised 46 MDS patients with bone marrow erythroblast frequencies of <50%. Three MDS patients that exhibited erythroid predominance achieved complete remission. The overall survival period (median: 15 months) of the erythroblast-predominant group was not inferior to that of the control group (median: 16 months). These results indicate that azacitidine is a promising treatment option for MDS/AEL irrespective of the numbers of erythroid cells in the patient's bone marrow.We reviewed the cases of 68 consecutive patients who were diagnosed with myelodysplastic syndrome (MDS, n=61) or acute erythroleukemia (AEL, n=7) according to the World Health Organization (WHO) 2008 criteria and had previously been treated with azacitidine, a hypomethylating agent. Fifteen MDS patients had bone marrow erythroblast frequencies of ≥50%, and 6 out of the 7 AEL patients were reclassified as MDS (refractory anemia with excess blasts [RAEB]-1: 1, RAEB-2: 5) according to the revised WHO 2016 criteria. There was no difference between the overall response ratio (41%), as determined by a hematological improvement in at least one of 3 lineages, of these erythroid rich patients and that of the control group, which comprised 46 MDS patients with bone marrow erythroblast frequencies of <50%. Three MDS patients that exhibited erythroid predominance achieved complete remission. The overall survival period (median: 15 months) of the erythroblast-predominant group was not inferior to that of the control group (median: 16 months). These results indicate that azacitidine is a promising treatment option for MDS/AEL irrespective of the numbers of erythroid cells in the patient's bone marrow. •HI could be achieved even if erythroblasts were dominant in BM.•The overall survival was also not inferior in erythroblast-predominant group.•Azacitidine could be an option irrespective of the numbers of erythroid cells in BM. We reviewed the cases of 68 consecutive patients who were diagnosed with myelodysplastic syndrome (MDS, n=61) or acute erythroleukemia (AEL, n=7) according to the World Health Organization (WHO) 2008 criteria and had previously been treated with azacitidine, a hypomethylating agent. Fifteen MDS patients had bone marrow erythroblast frequencies of ≥50%, and 6 out of the 7 AEL patients were reclassified as MDS (refractory anemia with excess blasts [RAEB]-1: 1, RAEB-2: 5) according to the revised WHO 2016 criteria. There was no difference between the overall response ratio (41%), as determined by a hematological improvement in at least one of 3 lineages, of these erythroid rich patients and that of the control group, which comprised 46 MDS patients with bone marrow erythroblast frequencies of <50%. Three MDS patients that exhibited erythroid predominance achieved complete remission. The overall survival period (median: 15 months) of the erythroblast-predominant group was not inferior to that of the control group (median: 16 months). These results indicate that azacitidine is a promising treatment option for MDS/AEL irrespective of the numbers of erythroid cells in the patient’s bone marrow. We reviewed the cases of 68 consecutive patients who were diagnosed with myelodysplastic syndrome (MDS, n=61) or acute erythroleukemia (AEL, n=7) according to the World Health Organization (WHO) 2008 criteria and had previously been treated with azacitidine, a hypomethylating agent. Fifteen MDS patients had bone marrow erythroblast frequencies of ≥50%, and 6 out of the 7 AEL patients were reclassified as MDS (refractory anemia with excess blasts [RAEB]-1: 1, RAEB-2: 5) according to the revised WHO 2016 criteria. There was no difference between the overall response ratio (41%), as determined by a hematological improvement in at least one of 3 lineages, of these erythroid rich patients and that of the control group, which comprised 46 MDS patients with bone marrow erythroblast frequencies of <50%. Three MDS patients that exhibited erythroid predominance achieved complete remission. The overall survival period (median: 15 months) of the erythroblast-predominant group was not inferior to that of the control group (median: 16 months). These results indicate that azacitidine is a promising treatment option for MDS/AEL irrespective of the numbers of erythroid cells in the patient's bone marrow. |
Author | Inoue, Morihiro Uchida, Tomoyuki Hua, Jian Hagihara, Masao |
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Cites_doi | 10.1182/blood-2008-10-182782 10.1007/s00277-012-1603-2 10.1111/j.1600-0609.2012.01816.x 10.1016/j.lrr.2013.04.001 10.1016/S1470-2045(09)70003-8 10.1182/blood-2016-03-643544 10.1182/blood-2009-09-243964 10.1186/1756-8722-6-32 10.3109/10428194.2015.1079318 10.1016/S0021-9258(19)68144-5 10.1016/j.leukres.2016.05.006 10.1200/JCO.2010.31.0854 10.1200/JCO.2016.66.9705 10.1182/blood-2009-03-209262 10.3324/haematol.2011.043687 10.1038/leu.2009.181 10.1038/modpathol.2008.142 10.1200/JCO.2009.23.8329 |
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Keywords | Azacitidine Myelodysplastic syndrome Acute erythroleukemia WHO |
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Snippet | •HI could be achieved even if erythroblasts were dominant in BM.•The overall survival was also not inferior in erythroblast-predominant group.•Azacitidine... Highlights • HI could be achieved even if erythroblasts were dominant in BM. • The overall survival was also not inferior in erythroblast-predominant group. •... We reviewed the cases of 68 consecutive patients who were diagnosed with myelodysplastic syndrome (MDS, n=61) or acute erythroleukemia (AEL, n=7) according to... |
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SubjectTerms | Acute erythroleukemia Adult Aged Aged, 80 and over Antimetabolites, Antineoplastic Antimetabolites, Antineoplastic - therapeutic use Azacitidine Azacitidine - pharmacology Bone Marrow Bone Marrow - pathology Case-Control Studies Erythroblasts Erythroblasts - pathology Female Hematology, Oncology and Palliative Medicine Humans Leukemia, Myeloid, Acute Leukemia, Myeloid, Acute - diagnosis Leukemia, Myeloid, Acute - drug therapy Male Middle Aged Myelodysplastic syndrome Myelodysplastic Syndromes Myelodysplastic Syndromes - diagnosis Myelodysplastic Syndromes - drug therapy Prognosis Remission Induction Remission Induction - methods Retrospective Studies WHO Young Adult |
Title | The effects of azacitidine on the response and prognosis of myelodysplastic syndrome and acute myeloid leukemia involving a bone marrow erythroblast frequency of >50 |
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