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. 2016 Feb 12;7(12):14251–14258. doi: 10.18632/oncotarget.7350

Table 1. Summary of clinicopathologic and cytogenetic findings of 32 myeloid neoplasms with isolated i(17q) cytogenetic abnormality.

Variable MDS/MPN (n = 13, 41%) AML (n = 17, 53%) MDS (n = 1, 3%) MPN (n = 1, 3%)
Median age (range) 64 years (51–83) 66 years (24–78) 55 years 60 years
Gender (female/male) 9/4 8/9 0/1 0/1
Hemoglobin* (g/dL) 9.4 (6.8–12.1) 10.1 (6.4–12.8) 8.6 12.9
MCV 88 (78–102) 88 (70–110) 91.5 104
Absolute neutrophil count*, × 109/L 3.6 (0.5–122.2) 3.0 (0–24.2) 1.9 5.7
Platelet count*, × 109/L 54 (10–143) 57 (15–271) 92 141
Peripheral blood blasts* (%) 1 (0–13) 26 (0–97) 0 1
Bone marrow blasts* (%) 8 (2–19) 37 (7–93) 12 0
Cytogenetic evolution, n (%) 30.8% 23.5%
Without clonal evolution 9 13 0 1
With clonal evolution 4 4 1 0
Survival 12 died, 1 lost to follow-up 14 died, 1 alive, 2 lost to follow-up Died Died
2008 WHO sub-classification CMML (n = 6) MDS/MPN-U (n = 5) aCML (n = 2) De novo/AML MRC (n = 9); sAML: h/o myeloid neoplasm (n = 5) and therapy-related (n = 2); AML, relapsed post-allogeneic SCT, unclassifiable (n = 1) RAEB-2 Post-ET MF

aCML, atypical chronic myeloid leukemia; AML, acute myeloid leukemia; AML MRC, AML with myelodysplasia-related changes; CMML, chronic myelomonocytic leukemia; MCV, mean corpuscular volume; MDS, myelodysplastic syndrome; MDS/MPN-U, myelodysplastic/myeloproliferative neoplasm unclassifiable; Post-Et MF, Post-essential thrombocythemia myelofibrosis; RAEB, refractory anemia with excess blasts; sAML, secondary AML; SCT, stem cell transplant.