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Chemotherapy for multiple myeloma.

Abstract
The effects of eight different drug combinations were evaluated in 256 patients with multiple myeloma. The response rate and time to remission were superior from regimens that added both vincristine and Adriamycin (doxorubicin) to an alkylating agent-prednisone combination. There was no improvement in response rate or survival time from two alternating drug combinations evaluated in an attempt to achieve more marked tumor reductions and to delay the emergence of resistant subclones. The addition of levamisole during remission maintenance did not improve survival time. Results supported the utility of unmaintained remission follow-up in selected patients with marked reductions in myeloma cell mass.
AuthorsR Alexanian, R Dreicer
JournalCancer (Cancer) Vol. 53 Issue 3 Pg. 583-8 (Feb 01 1984) ISSN: 0008-543X [Print] United States
PMID6362819 (Publication Type: Clinical Trial, Comparative Study, Journal Article, Randomized Controlled Trial)
Chemical References
  • Levamisole
  • Vincristine
  • Doxorubicin
  • Cyclophosphamide
  • Melphalan
  • Carmustine
  • Prednisone
Topics
  • Antineoplastic Combined Chemotherapy Protocols (therapeutic use)
  • Carmustine (administration & dosage)
  • Clinical Trials as Topic
  • Cyclophosphamide (administration & dosage)
  • Doxorubicin (administration & dosage)
  • Drug Administration Schedule
  • Humans
  • Levamisole (administration & dosage)
  • Melphalan (administration & dosage)
  • Multiple Myeloma (drug therapy)
  • Prednisone (administration & dosage)
  • Prognosis
  • Random Allocation
  • Vincristine (administration & dosage)

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