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Cyclophosphamide, bortezomib and dexamethasone induction for newly diagnosed multiple myeloma: high response rates in a phase II clinical trial.

Authors :
Reeder, C. B.
Reece, D. E.
Kukreti, V.
Chen, C.
Trudel, S.
Hentz, J.
Noble, B.
Pirooz, N. A.
Spong, J. E.
Piza, J. G.
Zepeda, V. H. J.
Mikhael, J. R.
Leis, J. F.
Bergsagel, P. L.
Fonseca, R.
Stewart, A. K.
Source :
Leukemia (08876924). Jul2009, Vol. 23 Issue 7, p1337-1341. 5p. 4 Charts, 2 Graphs.
Publication Year :
2009

Abstract

We have studied a three-drug combination with cyclophosphamide, bortezomib and dexamethasone (CyBorD) on a 28-day cycle in the treatment of newly diagnosed multiple myeloma (MM) patients to assess response and toxicity. The primary endpoint of response was evaluated after four cycles. Thirty-three newly diagnosed, symptomatic patients with MM received bortezomib 1.3 mg/m(2) intravenously on days 1, 4, 8 and 11, cyclophosphamide 300 mg/m(2) orally on days 1, 8, 15 and 22 and dexamethasone 40 mg orally on days 1-4, 9-12 and 17-20 on a 28-day cycle for four cycles. Responses were rapid with a mean 80% decline in the sentinel monoclonal protein at the end of two cycles. The overall intent to treat response rate (>or= partial response) was 88%, with 61% of very good partial response or better (>or=VGPR) and 39% of complete/near complete response (CR/nCR). For the 28 patients who completed all four cycles of therapy, the CR/nCR rate was 46% and VGPR rate was 71%. All patients undergoing stem cell harvest had a successful collection. Twenty-three patients underwent stem cell transplantation (SCT) and are evaluable through day 100 with CR/nCR documented in 70% and >or=VGPR in 74%. In conclusion, CyBorD produces a rapid and profound response in patients with newly diagnosed MM with manageable toxicity. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
08876924
Volume :
23
Issue :
7
Database :
Academic Search Index
Journal :
Leukemia (08876924)
Publication Type :
Academic Journal
Accession number :
43200693
Full Text :
https://doi.org/10.1038/leu.2009.26