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Conditioning Regimens

N-acetyl-L-cysteine does not affect the pharmacokinetics or myelosuppressive effect of busulfan during conditioning prior to allogeneic stem cell transplantation

Summary:

Busulfan is currently used as a main component in the conditioning regimen prior to allogeneic stem cell transplantation (SCT). Several studies have shown a correlation between exposure to busulfan and transplantation-related liver toxicity, such as venoocclusive disease (VOD) in patients undergoing SCT. Busulfan is metabolized mainly through glutathione (GSH). During high-dose therapy, busulfan may deplete hepatocellular levels of GSH. As part of the conditioning therapy, busulfan is usually followed by high doses of cyclophosphamide. The activation of cyclophosphamide yields a cytotoxic metabolite, 4-hydroxy cyclophosphamide, which is highly reactive and detoxified through GSH. According to recent studies using cell lines and animal models N-acetyl-L-cysteine (NAC), a GSH precursor, does not hamper the myeloablative effect of busulfan during conditioning. In the present study, we administered NAC during conditioning to 10 patients at risk of VOD due to pretransplant liver disorders or elevated liver enzymes. No side effects related to the NAC infusions were observed and busulfan concentrations were not affected. All patients became pancytopenic and engrafted with 100% donor cells. None of the patients developed VOD or liver failure. Increased liver enzymes during conditioning decreased or normalized in all patients. We suggest that NAC therapy is safe and does not impair the myeloablative effect of busulfan during conditioning prior to SCT.

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References

  1. Fried W, Kede A, Barone J . Effects of cyclophosphamide and busulfan on spleen-colony-forming units and on hematopoietic stroma. Cancer Res 1977; 37: 1205.

    CAS  PubMed  Google Scholar 

  2. Elson LA . Hematological effects of the alkylating agents. Ann NY Acad Sci 1958; 68: 826.

    Article  CAS  PubMed  Google Scholar 

  3. Santos WG, Tutschka PJ, Brookmeyer R et al. Marrow transplantation for acute nonlymphocytic leukemia after treatment with busulfan and cyclophosphamide. N Engl J Med 1983; 309: 1347–1353.

    Article  CAS  PubMed  Google Scholar 

  4. Tutschka PJ, Copelan EA, Klein JP . Bone marrow transplantation for leukemia following a new busulfan and cyclophosphamide regimen. Blood 1987; 70: 1382–1388.

    CAS  PubMed  Google Scholar 

  5. Ringdén O, Ruutu T, Remberger M et al. A randomised trial comparing busulfan with total body irradiation as conditioning in allogeneic marrow transplant recipients with leukemia: A report from the Nordic Bone Marrow Transplant Group. Blood 1994; 83: 2723–2730.

    PubMed  Google Scholar 

  6. Grochow LB, Jones RJ, Brundrett RB et al. Pharmacokinetics of busulfan: correlation with venoocclusive disease in patients undergoing bone marrow transplantation. Cancer Chemother Pharmacol 1989; 25: 55–61.

    Article  CAS  PubMed  Google Scholar 

  7. Bearman SI . The syndrome of hepatic venoocclusive disease after marrow transplantation. Blood 1995; 85: 3005.

    CAS  PubMed  Google Scholar 

  8. Shulman HM, Hinterberger W . Hepatic venoocclusive disease – liver toxicity syndrome after bone marrow transplantation. Transplantation 1992; 10: 197.

    CAS  Google Scholar 

  9. Carreras E, Granena A, Rozman C . Hepatic venoocclusive disease after bone marrow transplant. Blood Rev 1993; 7: 43.

    Article  CAS  PubMed  Google Scholar 

  10. McDonald GB, Sharma P, Matthews DE et al. Venoocclusive disease of the liver after bone marrow transplantation; diagnosis, incidence and predisposing factors. Hepatology 1984; 4: 116.

    Article  CAS  PubMed  Google Scholar 

  11. Jones RJ, Lee KSK, Beschorner WE et al. Venoocclusive disease of the liver following bone marrow transplantation. Transplantation 1987; 44: 778.

    Article  CAS  PubMed  Google Scholar 

  12. Allen JR, Carstens LA, Katagiri GJ . Hepatic veins of monkeys with venoocclusive disease. Arch Pathol 1969; 87: 279.

    CAS  PubMed  Google Scholar 

  13. Shulman HM, Gown Am, Nugent DJ . Hepatic venoocclusive disease after bone marrow transplantation. Am J Pathol 1987; 127: 549.

    CAS  PubMed  PubMed Central  Google Scholar 

  14. Carreras E . Venoocclusive disease of the liver after hematopoietic cell transplantation. Eur J Haematol 2000; 64: 281–291.

    Article  CAS  PubMed  Google Scholar 

  15. Marchand DH, Remmel RP, Abdel-Monem MM . Biliary excretion of a glutathione conjugate of busulfan and 1,4 diiodobutane in the rat. Drug Metab Dispos 1988; 16: 85–92.

    CAS  PubMed  Google Scholar 

  16. Hassan M, Ehrsson H . Metabolism of 14C-busulfan in isolated perfused rat liver. Eur J Drug Metab Pharmacokinet 1987; 12: 71–76.

    Article  CAS  PubMed  Google Scholar 

  17. Ritter CA, Bohnenstengel F, Hofmann Um Kroemer HK, Sperker B . Determination of tetrahydrothiophene formation as a probe of in vitro busulfan metabolism by human glutathione S-transferase A1-1: use of a highly sensitive gas chromatographic–mass spectrometric method. J Chromatogr B 1999; 730: 25–31.

    Article  CAS  Google Scholar 

  18. Czerwinski M, Gibbs JP, Slattery JT . Busulfan conjugation by glutathione S-transferase alpha my, and pi. Drug Metab Dispos 1996; 24: 1015–1019.

    CAS  PubMed  Google Scholar 

  19. Gibbs JP, Czerwinski M, Slattery JT . Busulfan-glutathione conjugation catalyzed by human liver cytosolic glutathione S-transferases. Cancer Res 1996; 56: 3678–3681.

    CAS  PubMed  Google Scholar 

  20. De Leve LD, Wang X . Role of oxidative stress and glutathione in busulfan toxicity in cultured murine hepatocytes. Pharmacology 200; 60: 143–154.

    Article  Google Scholar 

  21. Meister A . Glutathione metabolism and its selective modification. J Biol Chem 1988; 263: 17205–17208.

    CAS  PubMed  Google Scholar 

  22. Chyka PA, Butler AY, Holliman BJ, Herman MI . Utility of acetylcysteine in treating poisonings and adverse drug reactions. Drug Saf 2000; 22: 123–148.

    Article  CAS  PubMed  Google Scholar 

  23. Ringden O, Remberger M, Lehmann S et al. N-acetylcysteine for hepatic veno-occlusive disease after allogeneic stem cell transplantation. Bone Marrow Transplant 2000; 25: 993–996.

    Article  CAS  PubMed  Google Scholar 

  24. Czerwinski M, Kiem HP, Slattery JT . Human CD34+ cells do not express glutathione S-transferases alpha. Gene Ther 1997; 4: 268–270.

    Article  CAS  PubMed  Google Scholar 

  25. Wang L, Groves MJ, Hepburn MD, Bowen DT . Glutathione S-transferase enzyme expression in hematopoietic cell lines implies a different protective role for T1 and A1 isoenzymes in erythroid and for M1 in lymphoid lineages. Haematologica 2000; 85: 573–579.

    CAS  PubMed  Google Scholar 

  26. Hassan Z, Hellström-Lindberg E, Alsadi S et al. The effect of modulation of glutathione cellular content on busulfan induced toxicity on hematopoietic cells in vitro and in vivo. Bone Marrow Transplant 2002; 30: 141–147.

    Article  CAS  PubMed  Google Scholar 

  27. Hassan Z, Ljungman P, Ringdén O et al. Pharmacokinetics of liposomal busulfan in man. Bone Marrow Transplant 2000; 27: 479–485.

    Article  Google Scholar 

  28. Hassan M, Ehrsson H . Gas chromatographic determination of busulfan in plasma with electron–capture detection. J Chromatogr 1983; 277: 374–380.

    Article  CAS  PubMed  Google Scholar 

  29. Hassan M, Ljungman P, Ringdén O et al. The effect of busulfan on the pharmacokinetics of cyclophosphamide and its 4-hydroxy metabolite: time interval influence on therapeutic efficacy therapy related toxicity. Bone Marrow Transplant 2000; 25: 915–924.

    Article  CAS  PubMed  Google Scholar 

  30. Hassan M, Fasth A, Gerritsen B et al. Busulfan kinetics and limited sampling model in children with leukemia and inherited disorders. Bone Marrow Transplant 1996; 18: 843–850.

    CAS  PubMed  Google Scholar 

  31. Rindén O, Remberger M, Carlens S et al. Low incidence of acute graft-versus-host disease using unrelated HLA-A, -B and -DR compatible donors and conditioning including T-cell antibodies. Transplantation 1998; 66: 620–625.

    Article  Google Scholar 

  32. Prescott LF, Donovan JW, Jarvie DR, Proudfoot AT . The disposition and kinetics of intravenous N-acetylcysteine in patients with paracetamol over dosage. Eur J Clin Pharmacol 1989; 37: 501–506.

    Article  CAS  PubMed  Google Scholar 

  33. Rank N, Michel C, Haertel C et al. N-acetyl increases liver blood flow and improves liver function in septic shock patients: results of a prospective, randomized, double-blind study. Crit Care Med 2000; 28: 3799–3806.

    Article  CAS  PubMed  Google Scholar 

  34. Ahola T, Fellman V, Laaksonen R et al. Pharmacokinetics of intravenous N-acetylcysteine in pre-term new-born infants. Eur J Clin Pharmacol 1999; 55: 645–650.

    Article  CAS  PubMed  Google Scholar 

  35. Glucksberg H, Storb R, Fefer A et al. Clinical manifestation of graft-versus-host disease in human recipients of marrow from HLA-A matched sibling donors. Transplantation 1974; 18: 295–304.

    Article  CAS  PubMed  Google Scholar 

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Acknowledgements

This project was supported by grants from the Swedish Children Cancer Foundation (PROJ01/059, 1997/073), the Stockholm's Cancer Foundation (PROJ02/119), the Swedish Cancer Society (0070-B99-13XZC), the Swedish Medical Research Council (K2000-06X-05971-20A), the Cancer Society in Stockholm, the

Tobias Foundation, the FRF Foundation and Karolinska Institutet.

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Sjöö, F., Aschan, J., Barkholt, L. et al. N-acetyl-L-cysteine does not affect the pharmacokinetics or myelosuppressive effect of busulfan during conditioning prior to allogeneic stem cell transplantation. Bone Marrow Transplant 32, 349–354 (2003). https://doi.org/10.1038/sj.bmt.1704143

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