TY - JOUR
T1 - Extended follow-up of a phase 3 trial in relapsed multiple myeloma
T2 - Final time-to-event results of the APEX trial
AU - Richardson, Paul G.
AU - Sonneveld, Pieter
AU - Schuster, Michael
AU - Irwin, David
AU - Stadtmauer, Edward
AU - Facon, Thierry
AU - Harousseau, Jean Luc
AU - Ben-Yehuda, Dina
AU - Lonial, Sagar
AU - Goldschmidt, Hartmut
AU - Reece, Donna
AU - San Miguel, Jesus
AU - Bladé, Joan
AU - Boccadoro, Mario
AU - Cavenagh, Jamie
AU - Alsina, Melissa
AU - Rajkumar, S. Vincent
AU - Lacy, Martha
AU - Jakubowiak, Andrzej
AU - Dalton, William
AU - Boral, Anthony
AU - Esseltine, Dixie Lee
AU - Schenkein, David
AU - Anderson, Kenneth C.
PY - 2007/11/15
Y1 - 2007/11/15
N2 - Initial analysis of the Assessment of Proteasome Inhibition for Extending Remissions (APEX) trial of relapsed multiple myeloma patients showed significantly longer time to progression, higher response rate, and improved survival with single-agent bortezomib versus high-dose dexamethasone. In this updated analysis (median follow-up: 22 months), survival was assessed in both arms, and efficacy updated for the bortezomib arm. Median survival was 29.8 months for bortezomib versus 23.7 months for dexamethasone, a 6-month benefit, despite substantial crossover from dexamethasone to bortezomib. Overall and complete response rates with bortezomib were 43% and 9%, respectively; among responding patients, 56% improved response with longer therapy beyond initial response, leading to continued improvement in overall quality of response. Higher response quality (100% M-protein reduction) was associated with longer response duration; response duration was not associated with time to response. These data confirm the activity of bortezomib and support extended treatment in relapsed multiple myeloma patients tolerating therapy. This study is registered at http://clinicaltrials.gov (Study ID NCT00048230).
AB - Initial analysis of the Assessment of Proteasome Inhibition for Extending Remissions (APEX) trial of relapsed multiple myeloma patients showed significantly longer time to progression, higher response rate, and improved survival with single-agent bortezomib versus high-dose dexamethasone. In this updated analysis (median follow-up: 22 months), survival was assessed in both arms, and efficacy updated for the bortezomib arm. Median survival was 29.8 months for bortezomib versus 23.7 months for dexamethasone, a 6-month benefit, despite substantial crossover from dexamethasone to bortezomib. Overall and complete response rates with bortezomib were 43% and 9%, respectively; among responding patients, 56% improved response with longer therapy beyond initial response, leading to continued improvement in overall quality of response. Higher response quality (100% M-protein reduction) was associated with longer response duration; response duration was not associated with time to response. These data confirm the activity of bortezomib and support extended treatment in relapsed multiple myeloma patients tolerating therapy. This study is registered at http://clinicaltrials.gov (Study ID NCT00048230).
UR - http://www.scopus.com/inward/record.url?scp=35148825003&partnerID=8YFLogxK
U2 - 10.1182/blood-2006-08-036947
DO - 10.1182/blood-2006-08-036947
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C2 - 17690257
AN - SCOPUS:35148825003
SN - 0006-4971
VL - 110
SP - 3557
EP - 3560
JO - Blood
JF - Blood
IS - 10
ER -