Bortezomib plus melphalan and prednisone in elderly untreated patients with multiple myeloma:: results of a multicenter phase 1/2 study

被引:284
作者
Mateos, Maria-Victoria
Hernandez, Jose-M.
Hernandez, Miguel-T
Gutierrez, Norma-C.
Palomera, Luis
Fuertes, Marta
Diaz-Mediavilla, Joaquin
Lahuerta, Juan-J.
de la Rubia, Javier
Terol, Maria-Jose
Sureda, Ana
Bargay, Joan
Ribas, Paz
de Arriba, Felipe
Alegre, Adrian
Oriol, Albert
Carrera, Dolores
Garcia-Larana, Jos
Garcia-Sanz, Ramon
Blade, Joan
Prosper, Felipe
Mateo, Gemma
Esseltine, Dixie-Lee
de Velde, Helgi van
San Miguel, Jesus-F.
机构
[1] Millennium Pharmaceut Inc, Cambridge, MA USA
[2] Johnson & Johnson Pharmaceut Res & Dev, Raritan, NJ USA
关键词
D O I
10.1182/blood-2006-04-019778
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Standard first-line treatment for elderly multiple myeloma (MM) patients ineligible for stem cell transplantation is melphalan plus prednisone (MP). However, complete responses (CRs) are rare. Bortezomib is active in patients with relapsed MM, including elderly patients. This phase 1/2 trial in 60 untreated MM patients aged at least 65 years (half older than 75 years) was designed to determine dosing, safety, and efficacy of bortezomib plus MP (VMP). VMP response rate was 89%, including 32% immunofixation-negative CRs, of whom half of the IF- CR patients analyzed achieved immunophenotypic remission (no detectable plasma cells at 10(-4) to 10(-5) sensitivity). VMP appeared to overcome the poor prognosis conferred by retinoblastoma gene deletion and IgH translocations. Results compare favorably with our historical control data for MP-notably, response rate (89% versus 42%), event-free survival at 16 months (83% versus 51%), and survival at 16 months (90% versus 62%). Side effects were predictable and manageable; principal toxicities were hematologic, gastrointestinal, and peripheral neuropathy and were more evident during early cycles and in patients aged 75 years or more. In conclusion, in elderly patients ineligible for transplantation, the combination of bortezomib plus MID appears significantly superior to MP, producing very high CR rates, including immunophenotypic CRs, even in patients with poor prognostic features.
引用
收藏
页码:2165 / 2172
页数:8
相关论文
共 60 条
[1]   Development of the proteasome inhibitor PS-341 [J].
Adams, J .
ONCOLOGIST, 2002, 7 (01) :9-16
[2]   TREATMENT FOR MULTIPLE MYELOMA - COMBINATION CHEMOTHERAPY WITH DIFFERENT MELPHALAN DOSE REGIMENS [J].
ALEXANIAN, R ;
HAUT, A ;
KHAN, AU ;
LANE, M ;
MCKELVEY, EM ;
MIGLIORE, PJ ;
STUCKEY, WJ ;
WILSON, HE .
JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1969, 208 (09) :1680-+
[3]   Long-term outcomes of previously untreated myeloma patients: responses to induction chemotherapy and high-dose melphalan incorporated within a risk stratification model can help to direct the use of novel treatments [J].
Alvares, CL ;
Davies, FE ;
Horton, CS ;
Patel, G ;
Powles, R ;
Sirohi, B ;
Zuha, R ;
Gatt, A ;
Saso, R ;
Treleaven, JG ;
Dearden, CE ;
Potter, MN ;
Ethell, ME ;
Morgan, GJ .
BRITISH JOURNAL OF HAEMATOLOGY, 2005, 129 (05) :607-614
[4]  
[Anonymous], 1998, J Clin Oncol, V16, P3832
[5]   A prospective, randomized trial of autologous bone marrow transplantation and chemotherapy in multiple myeloma [J].
Attal, M ;
Harousseau, JL ;
Stoppa, AM ;
Sotto, JJ ;
Fuzibet, JG ;
Rossi, JF ;
Casassus, P ;
Maisonneuve, H ;
Facon, T ;
Ifrah, N ;
Payen, C ;
Bataille, R .
NEW ENGLAND JOURNAL OF MEDICINE, 1996, 335 (02) :91-97
[6]   Early mortality after diagnosis of multiple myeloma: Analysis of patients entered onto the United Kingdom Medical Research Council trials between 1980 and 2002 - Medical Research Council Adult Leukaemia Working Party [J].
Augustson, BM ;
Begum, G ;
Dunn, JA ;
Barth, NJ ;
Davies, F ;
Morgan, G ;
Behrens, J ;
Smith, A ;
Child, JA ;
Drayson, MT .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (36) :9219-9226
[7]   Total therapy 2 without thalidomide in comparison with total therapy 1: role of intensified induction and posttransplantation consolidation therapies [J].
Barlogie, B ;
Tricot, G ;
Rasmussen, E ;
Anaissie, E ;
van Rhee, F ;
Zangari, M ;
Fassas, A ;
Hollmig, K ;
Pineda-Roman, M ;
Shaughnessy, J ;
Epstein, J ;
Crowley, J .
BLOOD, 2006, 107 (07) :2633-2638
[8]   Total therapy with tandem transplants for newly diagnosed multiple myeloma [J].
Barlogie, B ;
Jagannath, S ;
Desikan, KR ;
Mattox, S ;
Vesole, D ;
Siegel, D ;
Tricot, G ;
Munshi, N ;
Fassas, A ;
Singhal, S ;
Mehta, J ;
Anaissie, E ;
Dhodapkar, D ;
Naucke, S ;
Cromer, J ;
Sawyer, J ;
Epstein, J ;
Spoon, D ;
Ayers, D ;
Cheson, B ;
Crowley, J .
BLOOD, 1999, 93 (01) :55-65
[9]   Standard chemotherapy compared with high-dose chemoradiotherapy for multiple myeloma: Final results of phase III US intergroup trial S9321 [J].
Barlogie, B ;
Kyle, RA ;
Anderson, KC ;
Greipp, PR ;
Lazarus, HM ;
Hurd, DD ;
McCoy, J ;
Dakhil, SR ;
Lanier, KS ;
Chapman, RA ;
Cromer, JN ;
Salmon, SE ;
Durie, B ;
Crowley, JC .
JOURNAL OF CLINICAL ONCOLOGY, 2006, 24 (06) :929-936
[10]   Phase I/II trial assessing bortezomlb and melphalan combination therapy for the treatment of patients with relapsed or refractory multiple myeloma [J].
Berenson, JR ;
Yang, HH ;
Sadler, K ;
Jarutirasarn, SG ;
Vescio, RA ;
Mapes, R ;
Purner, M ;
Lee, SP ;
Wilson, J ;
Morrison, B ;
Adams, J ;
Schenkein, D ;
Swift, R .
JOURNAL OF CLINICAL ONCOLOGY, 2006, 24 (06) :937-944