Therapeutic drug monitoring for busulfan in plasma during conditioning chemotherapy for autologous stem cell transplantation in relapsed primary cerebral lymphoma.

Therapeutic drug monitoring for busulfan in plasma during conditioning chemotherapy for autologous stem cell transplantation in relapsed primary cerebral lymphoma has not previously been reported. This case involved a 49-year-old man with relapsed primary cerebral lymphoma who received busulfan (8 mg/kg total dose; 2.67 mg/kg as a 3-hour IV infusion each of days -6 through -4) as part of a multiagent chemotherapy conditioning regimen. Multiple plasma samples were collected for all 3 doses and busulfan was quantified by liquid chromatography tandem mass spectrometry. A 1-compartment model was individually fitted to the concentration-time data for each dose. Clearance decreased across the 3 days of treatment (4.84, 4.06, and 3.04 mL/min/kg, respectively), whereas at the same times half-life increased (2.64, 3.18, and 4.17 hours, respectively), as did area under the plasma concentration-time curve0-infinity (9170, 10,900, and 14,600 microg h/L, respectively). Volume of distribution was similar across this time (1-1.1 L/kg). Indices of both renal and hepatic function did not indicate any significant diminution in likely clearance capacity for busulfan. There was also no compelling evidence for drug interactions that could decrease clearance. We conclude that therapeutic drug monitoring should be recommended for future cases of this rare disease, with a view to developing a target-concentration intervention strategy and improving outcomes.

[1]  M. Krajinovic,et al.  Influence of GST gene polymorphisms on busulfan pharmacokinetics in children , 2010, Bone Marrow Transplantation.

[2]  K. Hoang-Xuan,et al.  Primary CNS lymphoma in immunocompetent patients. , 2009, The oncologist.

[3]  B. Andersson,et al.  Busulfan in hematopoietic stem cell transplantation. , 2009, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

[4]  L. Deangelis,et al.  Primary central nervous system lymphoma: The role of consolidation treatment after a complete response to high‐dose methotrexate‐based chemotherapy , 2008, Cancer.

[5]  S. B. Kangarloo,et al.  Therapeutic drug monitoring of busulfan in transplantation. , 2008, Current pharmaceutical design.

[6]  K. Hoang-Xuan,et al.  Intensive chemotherapy followed by hematopoietic stem-cell rescue for refractory and recurrent primary CNS and intraocular lymphoma: Société Française de Greffe de Moëlle Osseuse-Thérapie Cellulaire. , 2008, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[7]  C. Uiterwaal,et al.  Once-daily intravenous busulfan with therapeutic drug monitoring compared to conventional oral busulfan improves survival and engraftment in children undergoing allogeneic stem cell transplantation. , 2008, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

[8]  S. Yun,et al.  Randomized comparison of four-times-daily versus once-daily intravenous busulfan in conditioning therapy for hematopoietic cell transplantation. , 2007, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

[9]  D. Niederwieser,et al.  Primary central nervous system lymphoma treated with high-dose methotrexate, high-dose busulfan/thiotepa, autologous stem-cell transplantation and response-adapted whole-brain radiotherapy: results of the multicenter Ostdeutsche Studiengruppe Hamato-Onkologie OSHO-53 phase II study. , 2007, Annals of oncology : official journal of the European Society for Medical Oncology.

[10]  L. Nguyen,et al.  Intravenous busulfan in adults prior to haematopoietic stem cell transplantation: a population pharmacokinetic study , 2005, Cancer Chemotherapy and Pharmacology.

[11]  M. Björkholm,et al.  Influence of prophylactic anticonvulsant therapy on high-dose busulphan kinetics , 2004, Cancer Chemotherapy and Pharmacology.

[12]  L. Grochow,et al.  Pharmacokinetics of busulfan: correlation with veno-occlusive disease in patients undergoing bone marrow transplantation , 2004, Cancer Chemotherapy and Pharmacology.

[13]  P. Ljungman,et al.  Population pharmacokinetic analysis resulting in a tool for dose individualization of busulphan in bone marrow transplantation recipients , 2001, Bone Marrow Transplantation.

[14]  S. Rodenhuis,et al.  Urinary excretion of thioTEPA and its metabolites in patients treated with high-dose cyclophosphamide, thioTEPA and carboplatin , 2001, Anti-cancer drugs.

[15]  K. Hoang-Xuan,et al.  Results of intensive chemotherapy followed by hematopoietic stem-cell rescue in 22 patients with refractory or recurrent primary CNS lymphoma or intraocular lymphoma. , 2001, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[16]  B. Andersson,et al.  Acute safety and pharmacokinetics of intravenous busulfan when used with oral busulfan and cyclophosphamide as pretransplantation conditioning therapy: a phase I study. , 2000, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

[17]  J. Gibbs,et al.  Plasma concentration monitoring of busulfan: does it improve clinical outcome? , 2000, Clinical pharmacokinetics.

[18]  M. Hassan The role of busulfan in bone marrow transplantation , 1999, Medical oncology.

[19]  M. Karlsson,et al.  Busulphan kinetics and limited sampling model in children with leukemia and inherited disorders. , 1996, Bone marrow transplantation.

[20]  A. Bosi,et al.  Itraconazole can increase systemic exposure to busulfan in patients given bone marrow transplantation. GITMO (Gruppo Italiano Trapianto di Midollo Osseo). , 1996, Anticancer research.

[21]  W. Tang,et al.  Conjugation of glutathione with a toxic metabolite of valproic acid, (E)-2-propyl-2,4-pentadienoic acid, catalyzed by rat hepatic glutathione-S-transferases. , 1996, Drug metabolism and disposition: the biological fate of chemicals.

[22]  V. Wiebe,et al.  Pharmacology of antineoplastic agents in pregnancy. , 1994, Critical reviews in oncology/hematology.

[23]  M. Weiss TOPFIT 2.0 Pharmacokinetic and Pharmacodynamic Data Analysis System for the PC, Günter Heinzel, Rolf Woloszcak, Peter Thomann. Gustav Fischer Verlag, Stuttgart-Jena-New York (1993), 647 pages. Soft cover DM 198.-. US-ISBN 1-56081-368-7., ISBN: 3-437-11486-7 , 1994 .