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PMID: 17451408 Published · ppublish English Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Safety and efficacy of bortezomib in high-risk and elderly patients with relapsed multiple myeloma.

British journal of haematology ·Vol. 137 ·No. 5 ·2007-06-00 ·Pages 429-35

Richardson PG, Sonneveld P, Schuster MW, Irwin D, Stadtmauer EA, Facon T, Harousseau JL, Ben-Yehuda D, Lonial S, San Miguel JF, Cavenagh JD, Anderson KC

Abstract

Adverse prognostic factors in multiple myeloma include advanced age, number of prior therapies, and higher International Staging System (ISS) disease stage. In the international, randomised, phase-3 Assessment of Proteasome Inhibition for Extending Remissions (APEX) study, bortezomib demonstrated significantly longer time to progression (TTP), higher response rates and improved survival compared with high-dose dexamethasone in patients with relapsed multiple myeloma following one to three prior therapies. In this APEX subgroup analysis, efficacy of bortezomib and dexamethasone was compared in elderly (age > or =65 years) and high-risk (>1 prior line of therapy; ISS stage II/III; refractory to prior therapy) patients. Bortezomib demonstrated substantial clinical activity in these patients. Response rate (34-40% vs. 13-19%), including complete response rate (5-8% vs. 0-1%), was significantly higher with bortezomib versus dexamethasone in all four subgroups. Similarly, median TTP was significantly longer with bortezomib versus dexamethasone, and 1-year survival probability was significantly higher in all subgroups. As in the total APEX population, rates of grade 3/4 adverse events were higher in bortezomib- versus dexamethasone-treated patients aged > or =65 years and with >1 prior line, while rates of serious adverse events were similar; toxicities generally proved manageable. Bortezomib should be considered an appropriate treatment for elderly and high-risk patients with relapsed multiple myeloma.

MeSH Terms
Aged Antineoplastic Agents/adverse effects,therapeutic use Boronic Acids/adverse effects,therapeutic use Bortezomib Chi-Square Distribution Dexamethasone/adverse effects,therapeutic use Disease Progression Disease-Free Survival Fatigue/chemically induced Glucocorticoids/adverse effects,therapeutic use Humans Multiple Myeloma/drug therapy Nausea/chemically induced Neutropenia/chemically induced Pyrazines/adverse effects,therapeutic use Risk Thrombocytopenia/chemically induced
Chemicals
Antineoplastic Agents Boronic Acids Glucocorticoids Pyrazines Bortezomib Dexamethasone
Authors & Affiliations
12 authors, click to expand affiliations / ORCID
Richardson Paul G
Medical Oncology, Dana-Farber Cancer Institute, 44 Binney Street, Boston, MA 02115, USA. paul_richardson@dfci.harvard.edu
Sonneveld Pieter
Schuster Michael W
Irwin David
Stadtmauer Edward A
Facon Thierry
Harousseau Jean-Luc
Ben-Yehuda Dina
Lonial Sagar
San Miguel Jesús-F
Cavenagh Jamie D
Anderson Kenneth C
Article Info
Journal
British journal of haematology
Abbr.
Br J Haematol
ISSN
0007-1048
Published
2007-06-00
Epub
2007-00-19
Pages
429-35
Language
English
Region
England
NLM ID
0372544
Subset
IM
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