A pilot study of 220 mg/m2 melphalan followed by autologous stem cell transplantation in patients with advanced haematological malignancies: pharmacokinetics and toxicity

Br J Haematol. 1996 Dec;95(3):527-30. doi: 10.1046/j.1365-2141.1996.d01-1932.x.

Abstract

We studied the pharmacokinetics and toxicity of 220 mg/m2 melphalan (HDM 220) followed by autologous stem cell transplantation in 16 patients with advanced haematological malignancies. Pharmacokinetic parameters (mean values of steady-state volume of distribution 14.6 l/m2, total body clearance 313 ml/min/m2, elimination half-life 46 min) were the same as those of 140 or 200 mg/m2 melphalan in previous reports. HDM 220 was feasible. Extramedullary toxicity was mainly W.H.O. grade 4 mucositis (13/16 patients). The median duration of 41 d (10, not reached) of thrombocytopenia < 25 x 10(9)/l was long. In multiple myeloma the response rate was 89% in heavily pretreated patients, suggesting that HDM 220 could be considered earlier in the course of the disease as an alternative consolidation therapy.

MeSH terms

  • Adolescent
  • Adult
  • Combined Modality Therapy
  • Female
  • Hematopoietic Stem Cell Transplantation / methods*
  • Hodgkin Disease / drug therapy
  • Hodgkin Disease / metabolism
  • Hodgkin Disease / therapy*
  • Humans
  • Leukemia, Myeloid, Acute / drug therapy
  • Leukemia, Myeloid, Acute / metabolism
  • Leukemia, Myeloid, Acute / therapy*
  • Lymphoma, Non-Hodgkin / drug therapy
  • Lymphoma, Non-Hodgkin / metabolism
  • Lymphoma, Non-Hodgkin / therapy*
  • Male
  • Melphalan / adverse effects
  • Melphalan / pharmacokinetics
  • Melphalan / therapeutic use*
  • Multiple Myeloma / drug therapy
  • Multiple Myeloma / metabolism
  • Multiple Myeloma / therapy*
  • Pilot Projects
  • Transplantation, Autologous

Substances

  • Melphalan