Skip to main content
Log in

High-dose carboplatin, cyclophosphamide, and BCNU with autologous bone marrow support: excessive hepatic toxicity

  • Short Communication
  • Published:
Cancer Chemotherapy and Pharmacology Aims and scope Submit manuscript

Summary

Intensive doses of carboplatin, cyclophosphamide, and BCNU with autologous bone marrow support were given to four patients with advanced melanoma. Three developed clinically diagnosed, severe venoocclusive liver disease, which was fatal in two cases. The dose of carboplatin (450 mg/m2) was comparable with that used in ambulatory regimens. At the doses and schedule employed, this three-drug combination produced excessive hepatic toxicity. Caution is suggested when giving carboplatin in combination with intensive doses of other chemotherapeutic agents with known hepatotoxic potential.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

References

  1. Calvert AM, Harland SJ, Newell DR (1982) Early clinical studies withcis-diammine-1,1-cyclobutanedicarboxylatoplatinum (II). Cancer Chemother Pharmacol 9: 140–147

    Article  PubMed  CAS  Google Scholar 

  2. Harrap KH, Jones M, Wilkinson CR, Clink H, Sparrow S, Mitchley B, Clarke S, Veasey A (1980) Antitumor, toxic and biochemical properties of cisplatin and other platinum complexes. In: Prestayko AW, Crooke ST, Carter SK (eds) Cisplatin, current advances and new developments. Academic Press, New York, pp 193–212

    Google Scholar 

  3. Jones RB, Shpall EJ, Shogan J, Moore J, Gockerman J, Peters WP (1988) AFM induction chemotherapy followed by intensive consolidation with autologous bone marrow (ABM) support for advanced breast cancer (abstract). Proc Am Assoc Clin Oncol 8: 8

    Google Scholar 

  4. McDonald GB, Sharma P, Matthews DE, (1981) Venoocclusive disease of the liver after bone marrow transplantation: diagnosis, incidence, and predisposing factors. Hepatology 4: 116–122

    Article  Google Scholar 

  5. Peters WP, Eder JP, Henner WD, Schryber S, Wilmore D, Finberg R, Schoenfeld D, Bast R, Gargone B, Antman K, Anderson J, Anderson K, Kruskall MS, Schnipper L, Frei E III (1986) High-dose combination alkylating agents with autologous bone marrow support: a phase I trial. J Clin Oncol 4: 646–654

    PubMed  CAS  Google Scholar 

  6. Peters WP, Shpall EJ, Jones RB, Olsen GA, Bast RC, Gockerman JP, Moore JO (1988) High-dose combination alkylating agents with bone marrow support as initial treatment for metastatic breast cancer. J Clin Oncol 6: 1368–1376

    PubMed  CAS  Google Scholar 

  7. Rollins BJ (1986) Hepatic veno-occlusive disease. Am J Med 81: 297–306

    Article  PubMed  CAS  Google Scholar 

  8. Shea TC, Flaherty M, Elias A, Eder JP, Antman K, Begg C, Schnipper L, Frei E III, Henner WD (1989) A phase I clinical and pharmacokinetic study of carboplatin and autologous bone marrow support. J Clin Oncol 7: 651–661

    PubMed  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

Supported in part by National Institutes of Health grant CA-14236-16

Rights and permissions

Reprints and permissions

About this article

Cite this article

Jones, R.B., Shpall, E.J., Ross, M. et al. High-dose carboplatin, cyclophosphamide, and BCNU with autologous bone marrow support: excessive hepatic toxicity. Cancer Chemother Pharmacol 26, 155–156 (1990). https://doi.org/10.1007/BF02897264

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF02897264

Keywords

Navigation