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. 2017 Jul 3;130(9):1125–1131. doi: 10.1182/blood-2017-05-783225

Table 1.

Patient characteristics at the start and end of ruxolitinib treatment (N = 86)

Parameter Baseline, N (%) At treatment discontinuation, N (%) P
Age ≥ 65 y 45 (52) 58 (67) <.0001
Sex (female) 36 (42) 36 (42)
Diagnosis
 Primary 56 (65) 56 (65)
 Post ET 9 (11) 9 (11)
 Post PV 21 (24) 21 (24)
Hgb < 10 g/dL 39 (45) 52 (61) .002
PLT, median (range), ×109/L 262 (13-1183) 91 (11-922) <.001
WBC ≥ 25 × 109/L 29 (34) 34 (40) .493
PB blasts ≥1% 44 (51) 51/80 (64) .356
PS > 0 73 (85) 80 (93) .053
Spleen size,* median (range), cm 20 (0-30) 14 (0-36) <.001
Transfusion-dependent 25 (29) 36/84 (43) .001
JAK2 allele burden (range), % 79 (20-99) 65 (6-99) .411
Cytogenetic
 Diploid 22/53 (42) 16/53 (30) <.0001
 Abnormal 31/53 (59) 37/53 (70)
Complex karyotype 7/53 (13) 13/53 (25) .007

BM, bone marrow; Hgb, hemoglobin; NA, not available; PB, peripheral blood; PLT, platelets; WBC, white blood cell count.

*

Evaluable for spleen size at baseline (82/86) and evaluable at discontinuation (68/86).

Data reported for 50 patients with cytogenetic information at baseline and follow-up. At baseline, 39/85 patients had abnormal cytogenetics (8 of which were complex karyotype). Complex karyotype is defined as 3 or more unrelated abnormalities.