4.4 Article

Effect of age on the pharmacokinetics of busulfan in patients undergoing hematopoietic cell transplantation; an alliance study (CALGB 10503, 19808, and 100103)

Journal

CANCER CHEMOTHERAPY AND PHARMACOLOGY
Volume 74, Issue 5, Pages 927-938

Publisher

SPRINGER
DOI: 10.1007/s00280-014-2571-0

Keywords

Busulfan; Bone marrow transplant; Elderly; Pharmacokinetics

Funding

  1. National Cancer Institute [CA31946, CA33601]
  2. Christiana Care Health Services, Inc. CCOP, Wilmington, DE [CA45418]
  3. Dana-Farber Cancer Institute, Boston, MA [CA32291]
  4. Monter Cancer Center of North Shore-LIJ Health Systems, Lake Success, NY [CA35279]
  5. Massachusetts General Hospital, Boston, MA [CA32291]
  6. Mount Sinai Medical Center, Miami, FL [CA45564]
  7. The Ohio State University Medical Center, Columbus, OH [CA77658]
  8. Rhode Island Hospital, Providence, RI [CA08025]
  9. Roswell Park Cancer Institute, Buffalo, NY [CA59518]
  10. University of California at San Francisco, San Francisco, CA [CA60138]
  11. University of Chicago, Chicago, IL [CA41287]
  12. University of Maryland Greenebaum Cancer Center, Baltimore, MD [CA31983]
  13. University of Massachusetts Medical School, Worcester, MA [CA37135]
  14. University of Minnesota, Minneapolis, MN [CA16450]
  15. University of Nebraska Medical Center, Omaha, NE [CA77298]
  16. University of North Carolina at Chapel Hill, Chapel Hill, NC [CA47559]
  17. University of Vermont, Burlington, VT [CA77406]
  18. Wake Forest University School of Medicine, Winston-Salem, NC [CA03927]
  19. Washington University School of Medicine, St. Louis, MO [CA77440]
  20. Weill Medical College of Cornell University, New York, NY [CA07968]
  21. Western Pennsylvania Cancer Institute, Pittsburgh, PA [CA31946]
  22. Dartmouth Medical School-Norris Cotton Cancer Center, Lebanon, NH [CA04326]
  23. Walter Reed Army Medical Center, Washington, DC [CA26806]
  24. [P30CA047904]

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Older patients with acute myeloid leukemia (AML) and myelodysplastic syndrome have often been excluded from myeloablative-conditioning regimens containing busulfan because of non-disease-related morbidity and mortality. We hypothesized that busulfan clearance (BuCL) in older patients (> 60 years) would be reduced compared to that in younger patients, potentially explaining observed differences in busulfan tolerability. AML patients in three CALGB hematopoietic cell transplantation studies were treated with a conditioning regimen using IV busulfan, dosed at 0.8 mg/kg. Plasma busulfan concentrations were determined by LC-MS and analyzed by non-compartmental methods. BuCL was normalized to actual (ABW), ideal (IBW), or corrected (CBW) body weight (kg). Differences in BuCL between age groups were examined using the Wilcoxon rank sum test. One hundred and eighty-five patients were accrued; 174 provided useable pharmacokinetic data. Twenty-nine patients a parts per thousand yen60 years old (median 66; range 60-74) had a significantly higher BuCL versus those < 60 years old (median 50; range 18-60): BuCL 236 versus 168 mL/min, p = 0.0002; BuCL/ABW 3.0 versus 2.1 mL/min/kg, p = 0.0001; BuCL/IBW 3.8 versus 2.6 mL/min/kg, p = 0.0035; BuCL/CBW 3.4 versus 2.6 mL/min/kg, p = 0.0005. Inter-patient variability in clearance (CV %) was up to 48 % in both age groups. Phenytoin administration, a potential confounder, did not affect BuCL, regardless of weight normalization (p > 0.34). Contrary to our hypothesis, BuCL was significantly higher in older patients compared to younger patients in these studies and does not explain the previously reported increase in busulfan toxicity observed in older patients.

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