• J Perkins, T Field, J Kim, M A Kharfan-Dabaja, E Ayala, L Perez, H Fernandez, K Fancher, C Tate, L M Shaw, M C Milone, J A Gardiner, S Miller, and C Anasetti.
• Blood and Marrow Transplant Program, H. Lee Moffitt Cancer Center, Tampa, FL 33612, USA. Janelle.perkins@moffitt.org
• Bone Marrow Transplant. 2011 Nov 1; 46 (11): 1418-25.

AbstractWe used pharmacokinetic (PK) targeting of BU in 145 consecutive patients treated with fludarabine and i.v. BU. BU was given once daily at 130 mg/m(2) per day on days 1 and 2; doses for days 3 and 4 were adjusted in 92 patients (63%) to an average daily area under the concentration-time curve (AUC) of 5300 μM/min. In the remaining 53 patients, the first-dose AUC was within the target range and no dosing adjustments were required. First-dose AUC, maximum concentration and clearance were not correlated with age, race, ethnicity, performance status, or hematopoietic cell transplant comorbidity index. Women had higher clearance than men (median 2.9 vs 2.5 mL/min/kg; P=0.001). BU toxicities were not associated with first-dose AUC or any other PK parameter measured. First-dose BU AUC was not associated with non-relapse mortality (NRM) or survival, but higher AUC was predictive of relapse. We did not find an increased risk of toxicity or NRM in patients with high first-dose AUC presumably because of the dose adjustment. We conclude that PK targeting of BU as described here provides a simple, safe and effective method of delivering high BU doses before transplantation in a wide variety of patients.

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