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Primary dexamethasone treatment of multiple myeloma

Open access
Alexanian, R, Dimopoulos, MA, Delasalle, K, Barlogie, B·1992·Blood

Abstract

Intermittent courses of dexamethasone (DEX) were administered to 112 consecutive, previously untreated patients with multiple myeloma (MM). Using criteria based on a 75% or greater reduction of calculated tumor mass, the overall response rate was 43%. Among comparable patients, response rate were approximately 15% less than those observed previously with vincristine-doxorubicin by continuous infusion with intermittent DEX (VAD) and similar to those with melphalan-prednisone. The projected survival times with VAD or DEX were similar. Results indicated that DEX accounted for most of the plasma cell reduction achieved with VAD. Serious complications occurred in 27% of patients treated with VAD, but in only 4% of those who received DEX. In view of the similar outcome with fewer serious complications, DEX provided a simple, effective, and safe primary treatment for a large fraction of patients with MM. Patients who appear most likely to benefit include those with hypercalcemia or pancytopenia, or who require simultaneous radiotherapy for a pathologic fracture.

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Metadata

Authors
Alexanian, R., Dimopoulos, M., Delasalle, K., & Barlogie, B.
Venue
Blood
Published
1992-08-15
Volume
80
Issue
4
Pages
887-890
ISSN
  • 0006-4971 (ISSN-L)
  • 1528-0020
OpenAlex
W2264313156
Cited by
366
References
0
FWCI
6.41
Type
journal article
Language
en
Open access
bronze

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CoChat. (2026). Citation check: Primary dexamethasone treatment of multiple myeloma. https://app.cochat.ai/papers/10.1182/blood.v80.4.887.887
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Alexanian, R., Dimopoulos, M., Delasalle, K., & Barlogie, B. (1992). Primary dexamethasone treatment of multiple myeloma. Blood. https://doi.org/10.1182/blood.v80.4.887.887

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.