Table 1.
Age and sex | |
Age at diagnosis (y, range) | 69 (27–87) |
Female (n, %) | 23/57 (40) |
Male (n, %) | 34/57 (60) |
WHO-2016 diagnosis | |
MDS-MLD | 28/57 (49) |
MDS-SLD | 7/57 (12) |
MDS-EB1 | 11/57 (19) |
MDS-EB2 | 2/57 (4) |
MDS-RS-MLD | 1/57 (2) |
CMML | 5/57 (9) |
MDS/MPN (not CMML) | 1/57 (2) |
MDS-U | 2/57 (4) |
Bone marrow features at diagnosis (n, %) | |
Available core biopsy at diagnosis | 43/57 (75) |
Hypocellular (cellularity <25%) | 9/43 (21) |
Fibrosis MF 0–1 | 30/43 (70) |
Fibrosis MF 2 | 11/43 (26) |
MF-not evaluated | 2/43 (5) |
IPSS at diagnosis (n, %), only for MDS (n = 51) | |
Low | 17/51 (33) |
Int-1 | 34/51 (67) |
IPSS-R at diagnosis (n, %), only for MDS (n = 51) | |
Very low | 2/51 (4) |
Low | 21/51 (41) |
Intermediate | 15/51 (29) |
High | 9/51 (18) |
Very high | 4/51 (8) |
Blood counts before treatment | |
Hb (g/dL) | 11.1 (6.9–15.7) |
PLT (103/μL) | 20 (2–49) |
ANC (103/μL) | 2.00 (0.26–20.4) |
Danazol dosing and timing | |
Mean daily dose (mg, range) | 500 (88–667) |
Dose reductions due to any cause (n, %) | 19/57 (33) |
Median treatment duration (mo, range) | 12.0 (0.6–149.5) |
Concomitant treatments at danazol start (n, %) | |
Erythropoiesis stimulating agents | 5/57 (9) |
Corticosteroids | 12/57 (21) |
Cyclosporin A | 1/57 (2) |
No concomitant treatments | 41/57 (72) |
Response data | |
Median follow-up (mo, range) | 16.2 (0.7–171) |
PLT response (n, %) | 29/57 (51) |
Median time to PLT response (mo, range) | 3.3 (1.3–24.6) |
Erythroid hematological improvement (n, %) | 10/24 (42) |
Neutrophil hematological improvement (n, %) | 4/9 (44) |
ANC = absolute neutrophil count; CMML = chronic myelomonocytic leukemia; Hb = hemoglobin; IPSS = International Prognostic Scoring System; IPSS-R = revised International Prognostic Scoring System; MDS/MPN = myelodysplastic syndrome/myeloproliferative neoplasms; MDS EB1 = myelodysplastic syndrome with excess blast 1; MDS EB2 = myelodysplastic syndrome with excess blast 2; PLT = platelet.