Clinical characteristics of patients participating in this study
. | No. . |
---|---|
MDS | 88 |
Low risk | 58 |
RCUD/RCMD/5q−/MDS-U* | 38 |
RARS | 20 |
High risk | |
RAEB 1/2* | 30 |
MDS/MPN | 66 |
CMML/aCML/JMML | 48 |
MDS/MPN-U* (RARS-T) | 18 (11) |
MPN | 52 |
PV/PMF/ET | 16 |
CML | 36 |
AML | 109 |
Primary AML | 55 |
Secondary AML* | 54 |
. | No. . |
---|---|
MDS | 88 |
Low risk | 58 |
RCUD/RCMD/5q−/MDS-U* | 38 |
RARS | 20 |
High risk | |
RAEB 1/2* | 30 |
MDS/MPN | 66 |
CMML/aCML/JMML | 48 |
MDS/MPN-U* (RARS-T) | 18 (11) |
MPN | 52 |
PV/PMF/ET | 16 |
CML | 36 |
AML | 109 |
Primary AML | 55 |
Secondary AML* | 54 |
MDS indicates myelodysplastic syndromes; RCUD, refractory cytopenia with unilineage dysplasia; RCMD, refractory cytopenia with multilineage dysplasia; MDS-U, MDS unclassifiable; RARS, refractory anemia with ring sideroblasts; RAEB, refractory anemia with excess blasts; MDS/MPN, MDS/myeloproliferative neoplasms; CMML, chronic myelomonocytic leukemia; aCML, atypical chronic myeloid leukemia; JMML, juvenile myelomonocytic leukemia; RARS-T, RARS associated with marked thrombocytosis; PV, polycythemia vera; PMF, primary myelofibrosis; ET, essential thrombocythemia; and AML, acute myeloid leukemia.
Eight cases included with therapy-related myeloid malignancies.