Investigational New Drugs

, Volume 24, Issue 5, pp 393–401

Disposition of 9-nitrocamptothecin and its 9-aminocamptothecin metabolite in relation to ABC transporter genotypes

  • William C. Zamboni
  • Ramesh K. Ramanathan
  • Howard L. McLeod
  • Sridhar Mani
  • Douglas M. Potter
  • Sandra Strychor
  • Lauren J. Maruca
  • Cristi R. King
  • Laura L. Jung
  • Robert A. Parise
  • Merrill J. Egorin
  • Todd A. Davis
  • Sharon Marsh
Preclinical Studies

DOI: 10.1007/s10637-006-6335-5

Cite this article as:
Zamboni, W.C., Ramanathan, R.K., McLeod, H.L. et al. Invest New Drugs (2006) 24: 393. doi:10.1007/s10637-006-6335-5
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Summary

Purpose: The source of the pharmacokinetic variability of 9-nitrocamptothecin (9NC) and its 9-aminocamptothecin (9AC) metabolite is unknown. ATP-binding cassette (ABC) transporters have been reported to modulate camptothecin analogues, are associated with camptothecin resistance, and might also affect 9NC and 9AC pharmacokinetics. The aim of this study was to evaluate the functional consequence of known single nucleotide polymorphisms in the transporter genes ABCB1, ABCC2, and ABCG2 on the pharmacokinetic disposition of 9NC and 9AC. Experimental design: Pharmacokinetic and genotyping studies were performed in 55 patients as part of two phase I studies of 9NC in patients with refractory solid tumors, a phase II study of 9NC in patients with advanced colon cancer, and a study evaluating the disposition of 9NC after administration of a single dose under fasting conditions. DNA was isolated from plasma and analyzed for variants in ABCB1, ABCC2, and ABCG2 genes. The ABCB1 1236C>T (n = 43), ABCB1 2677G>T/A (n = 43), ABCB1 3435C>T (n = 43), ABCC2 3972C>T (n = 39), and ABCG2 421C>A (n = 42) variants were analyzed using Pyrosequencing. Results: The ABCG2 421C>A genotype significantly affected the pharmacokinetics of 9AC. The mean 9AC lactone AUC/dose for wild-type (n = 25) and heterozygous (n = 2) patients were 14.3 ng/mL · h and 51.1 ng/mL. h, respectively (P = 0.032). The mean ± SD 9AC total AUC/dose for wild-type (n = 39) and heterozygous (n = 3) patients were 91.9 ± 78.3 ng/mL · h and 129.0 ± 90.5 ng/mL · h, respectively (P = 0.40). 9NC and 9AC disposition were not significantly influenced by variants in ABCB1, ABCC2, and ABCG2, and ABCB1 and ABCC2, respectively (P>0.05). Conclusion: These findings suggest that inter-individual variability in 9AC disposition, but not 9NC, may be influenced, in part, by ABCG2 genotype. In contrast, there was no evidence for a relationship between ABCG2 and the disposition of 9NC, or for relationships between ABCB1 and ABCC2 genotypes and the disposition of 9NC or 9AC.

Keywords

ABC transportersGenotypingPharmacogenetics9AC9NC

Copyright information

© Springer Science + Business Media, LLC 2006

Authors and Affiliations

  • William C. Zamboni
    • 1
    • 2
    • 3
    • 8
  • Ramesh K. Ramanathan
    • 1
    • 3
  • Howard L. McLeod
    • 4
  • Sridhar Mani
    • 5
  • Douglas M. Potter
    • 6
    • 7
  • Sandra Strychor
    • 1
  • Lauren J. Maruca
    • 1
  • Cristi R. King
    • 4
  • Laura L. Jung
    • 1
  • Robert A. Parise
    • 1
  • Merrill J. Egorin
    • 1
    • 3
  • Todd A. Davis
    • 4
  • Sharon Marsh
    • 4
  1. 1.Molecular Therapeutics Drug Discovery ProgramUniversity of Pittsburgh Cancer InstitutePittsburgh
  2. 2.Department of Pharmaceutical Sciences, School of PharmacyUniversity of PittsburghPittsburgh
  3. 3.Division of Hematology/Oncology, Department of Medicine, School of MedicineUniversity of PittsburghPittsburgh
  4. 4.Department of MedicineWashington University School of MedicineSt. Louis
  5. 5.Medicine, Oncology, and Molecular GeneticsAlbert Einstein College of MedicineBronx
  6. 6.Department of Biostatistics, Graduate School of Public HealthUniversity of PittsburghPittsburgh
  7. 7.Biostatistics FacilityUniversity of Pittsburgh Cancer InstitutePittsburgh
  8. 8.University of Pittsburgh Cancer InstituteHillman Cancer Research CenterPittsburgh