Melphalan, prednisone, and lenalidomide treatment for newly diagnosed myeloma:: A report from the GIMEMA -: Italian multiple myeloma network

被引:241
作者
Palumbo, Antonio
Falco, Patrizia
Corradini, Paolo
Falcone, Antonietta
Di Raimondo, Francesco
Giuliani, Nicola
Crippa, Claudia
Ciccone, Giovannino
Omede, Paola
Ambrosini, Maria Teresa
Gay, Francesca
Bringhen, Sara
Musto, Pellegrino
Foa, Robin
Knight, Robert
Zeldis, Jerome B.
Boccadoro, Mario
Petrucci, Maria Teresa
机构
[1] Univ Turin, Azienda Osped S Giovanni Battista, Div Ematol, I-10126 Turin, Italy
[2] Ist Nazl Tumori, Div Ematol, I-20133 Milan, Italy
[3] IRCCS Casa Sollievo Sofferenza, UP Ematol & Trapianto Cellule Staminali, San Giovanni Rotondo, Italy
[4] Osped Ferrarotto, Catania, Italy
[5] Univ Parma, Cattedra & UO Ematol & Trapianti Midollo, I-43100 Parma, Italy
[6] Univ Brescia, Spedali Civili, Sez Ematol, Brescia, Italy
[7] Univ Turin, Azienda Osped S Giovanni Battista, Serv Epidemiol Tumori, I-10126 Turin, Italy
[8] CROB, UO Ematol & Traipanto Cellule Staminali, Rome, Italy
[9] Univ Roma La Sapienza, Dipartimento Biotecnol & Ematol, Rome, Italy
[10] Celgene Corp, Summit, NJ USA
关键词
D O I
10.1200/JCO.2007.12.3463
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose Lenalidomide has shown significant antimyeloma activity in clinical studies. Oral melphalan, prednisone, and thalidomide have been regarded as the standard of care in elderly multiple myeloma patients. We assessed dosing, efficacy, and safety of melphalan, prednisone, and lenalidomide (MPR) in newly diagnosed elderly myeloma patients. Patients and Methods Oral melphalan was administered in doses ranging from 0.18 to 0.25 mg/kg on days 1 to 4, prednisone at a 2-mg/kg dose on days 1 to 4, and lenalidomide at doses ranging from 5 to 10 mg on days 1 to 21, every 28 days for nine cycles, followed by maintenance therapy with lenalidomide alone. Aspirin was given as a prophylaxis for thrombosis. Results Fifty-four patients were enrolled and evaluated after completing the assigned treatment schedule. The maximum tolerated dose was defined as 0.18 mg/kg melphalan and 10 mg lenalidomide. With these doses, 81% of patients achieved at least a partial response, 47.6% achieved a very good partial response, and 23.8% achieved a complete immunofixation-negative response. In all patients, 1-year event-free and overall survival rates were 92% and 100%, respectively. At the maximum tolerated dose, grade 3 adverse events included neutropenia (38.1%), thrombocytopenia (14.2%), febrile neutropenia (9.5%), vasculitis (9.5%), and thromboembolism (4.8%); grade 4 adverse events were neutropenia (14.2%) and thrombocytopenia (9.5%). Conclusion Oral MPR therapy is a promising first-line treatment for elderly myeloma patients. Hematologic adverse events were frequent but manageable. A low incidence of nonhematologic adverse events was noted. Aspirin appears to provide adequate antithrombosis prophylaxis.
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收藏
页码:4459 / 4465
页数:7
相关论文
共 35 条
[1]   A novel three-color, clone-specific fluorescence in situ hybridization procedure for monoclonal gammopathies [J].
Ahmann, GJ ;
Jalal, SM ;
Juneau, AL ;
Christensen, ER ;
Hanson, CA ;
Dewald, GW ;
Greipp, PR .
CANCER GENETICS AND CYTOGENETICS, 1998, 101 (01) :7-11
[2]  
[Anonymous], 1998, J Clin Oncol, V16, P3832
[3]   Single versus double autologous stem-cell transplantation for multiple myeloma [J].
Attal, M ;
Harousseau, JL ;
Facon, T ;
Guilhot, F ;
Doyen, C ;
Fuzibet, JG ;
Monconduit, M ;
Hulin, C ;
Caillot, D ;
Bouabdallah, R ;
Voillat, L ;
Sotto, JJ ;
Grosbois, B ;
Bataille, R .
NEW ENGLAND JOURNAL OF MEDICINE, 2003, 349 (26) :2495-2502
[4]   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
[5]   Thalidomide and hematopoietic-cell transplantation for multiple myeloma [J].
Barlogie, B ;
Tricot, G ;
Anaissie, E ;
Shaughnessy, J ;
Rasmussen, E ;
van Rhee, F ;
Fassas, A ;
Zangari, M ;
Hollmig, K ;
Pineda-Roman, M ;
Lee, C ;
Talamo, G ;
Thertulien, R ;
Kiwan, E ;
Krishna, S ;
Fox, M ;
Crowley, J .
NEW ENGLAND JOURNAL OF MEDICINE, 2006, 354 (10) :1021-1030
[6]   Timeline - The evolution of thalidomide and its IMiD derivatives as anticancer agents [J].
Bartlett, JB ;
Dredge, K ;
Dalgleish, AG .
NATURE REVIEWS CANCER, 2004, 4 (04) :314-322
[7]  
Blade Joan, 1998, British Journal of Haematology, V102, P1115, DOI 10.1046/j.1365-2141.1998.00930.x
[8]   MULTIPLE-MYELOMA - VMCP/VBAP ALTERNATING COMBINATION CHEMOTHERAPY IS NOT SUPERIOR TO MELPHALAN AND PREDNISONE EVEN IN HIGH-RISK PATIENTS [J].
BOCCADORO, M ;
MARMONT, F ;
TRIBALTO, M ;
AVVISATI, G ;
ANDRIANI, A ;
BARBUI, T ;
CANTONETTI, M ;
CAROTENUTO, M ;
COMOTTI, B ;
DAMMACCO, F ;
FRIERI, R ;
GALLAMINI, A ;
GALLONE, G ;
GIOVANGROSSI, P ;
GRIGNANI, F ;
LAUTA, VM ;
LIBERATI, M ;
MUSTO, P ;
NERETTO, G ;
PETRUCCI, MT ;
RESEGOTTI, L ;
PILERI, A ;
MANDELLI, F .
JOURNAL OF CLINICAL ONCOLOGY, 1991, 9 (03) :444-448
[9]   Cancer incidence and mortality in Europe, 2004 [J].
Boyle, P ;
Ferlay, J .
ANNALS OF ONCOLOGY, 2005, 16 (03) :481-488
[10]  
*CANC THER EV PROG, 2003, COMM TERM CRIT ADV E