Variable | CKD Group (n = 8) | No CKD Group (n = 25) | p-value |
---|---|---|---|
Age (years) | 60 (36–86) | 43 (29–70) | 0.008 |
Sex (male/female) | 5/3 | 17/8 | 1.000 |
CML/Ph-ALL | 6/2 | 24/1 | 0.139 |
Serum creatinine level (mg/dL) at baseline | 0.93 (0.55–1.02) | 0.78 (0.53–1.12) | 0.435 |
eGFR (mL/min/1.73 m2) at baseline | 68 (61–77) | 80 (55–103) | 0.003 |
Hypertension | 2 | 2 | 0.062 |
Diabetes mellitus | 0 | 4 | 1.000 |
Common dasatinib-related adverse eventsa) | 5 | 13 | 1.000 |
Pleural effusion | 3 | 7 | 0.623 |
Lymphocytosis | 1 | 17 | 0.012 |
Lymphopenia | 2 | 3 | 0.574 |
Concomitant potential nephrotoxic agents | 3 | 6 | 0.651 |
Concomitant use of diuretics | 3 | 8 | 0.420 |
Median lymphocyte count (/μL) | 2025 (780–3413) | 2760 (1089–6200) | 0.089 |
Maximal lymphocyte count (/μL) | 3279 (1246–4183) | 4813 (2075–10,545) | 0.001 |
Minimum lymphocyte count (/μL) | 896 (390–2136) | 1184 (484‒2288) | 0.127 |
Maximal-baseline lymphocyte count ratio | 1.5 (1.0–3.8) | 2.2 (0.8–9.3) | 0.176 |
Median NLR | 1.59 (0.75–4.58) | 1.21 (0.40–2.22) | 0.136 |
History of TKI(s) prior to dasatinib | 6 | 14 | 0.431 |
(Imatinib/nilotinib/Both) | (3/1/2) | (8/3/3) |