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Related Experiment Videos

High-dose intravenous melphalan: a review

B L Samuels1, J D Bitran

  • 1Department of Medicine, Lutheran General Hospital, University of Chicago School of Medicine, Park Ridge, IL, USA.

Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|July 1, 1995
PubMed
Summary

High-dose melphalan (HDM) shows significant clinical activity in relapsed cancers like myeloma and neuroblastoma. Its favorable toxicity profile and availability of progenitor cells allow for repeated treatments, establishing it as an effective salvage and consolidative therapy.

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Area of Science:

  • Pharmacology and clinical trials
  • Oncology and hematology

Background:

  • Intravenous high-dose melphalan (HDM) is a chemotherapy agent.
  • Autologous bone marrow support (ABMS) or peripheral-blood progenitor cells (PBPCs) are used with HDM.

Purpose of the Study:

  • To review the clinical pharmacology of HDM.
  • To review clinical trials that have used HDM.

Main Methods:

  • Reviewed mechanism of action, clinical pharmacology, and clinical studies of HDM.
  • Included studies in myeloma, ovarian cancer, lymphoma, breast cancer, neuroblastoma, Ewing's sarcoma, and acute leukemia.
  • Considered HDM with and without ABMS or PBPCs.

Main Results:

  • HDM exhibits a short distribution half-life (5-15 min) and elimination half-life (17-75 min) with significant variability.

Related Experiment Videos

  • Demonstrated clinical activity in relapsed multiple myeloma, ovarian cancer, Hodgkin's disease, breast cancer, and neuroblastoma.
  • Toxicities include myelosuppression, nausea, vomiting, mucositis, diarrhea, and hepatic veno-occlusive disease.
  • Conclusions:

    • HDM is an established salvage regimen for relapsed neuroblastoma and consolidative treatment for high-risk neuroblastoma.
    • HDM is emerging as an effective treatment for stage II and III myeloma.
    • Favorable toxicity and PBPC availability permit repetitive HDM therapy.