Choosing treatment options for patients with relapsed/refractory multiple myeloma

被引:7
作者
Castelli, Roberto [1 ,2 ]
Orofino, Nicola [1 ]
Losurdo, Agnese [1 ]
Gualtierotti, Roberta [1 ]
Cugno, Massimo [1 ,2 ]
机构
[1] Univ Milan, Dept Pathophysiol & Transplantat, Milan, Italy
[2] IRCCS Fdn Ca Granda Policlin, Dept Med, Milan, Italy
关键词
immunomodulatory drugs; proteasome inhibitors; relapsed/refractory multiple myeloma; salvage therapies; STEM-CELL TRANSPLANTATION; LENALIDOMIDE PLUS DEXAMETHASONE; SINGLE-AGENT CARFILZOMIB; THALIDOMIDE-DEXAMETHASONE; INTRAVENOUS MELPHALAN; OPEN-LABEL; FOLLOW-UP; MYELODYSPLASTIC SYNDROMES; IMMUNOMODULATORY DRUGS; MARROW-TRANSPLANTATION;
D O I
10.1586/14737140.2014.863153
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Multiple myeloma (MM) is a clonal plasma cell disorder that is still incurable using conventional treatments. Over the last decade, advances in front-line therapy have led to an increase in survival, but there are still some doubts in the case of relapsed/refractory disease. We searched the PubMed database for articles on treatment options for patients with relapsed/refractory MM published between 1996 and 2013. These treatments included hematopoietic cell transplantation (HCT), rechallenges using previous chemotherapy regimens, and trials of new regimens. The introduction of new agents such as the immunomodulatory drugs (IMIDs) thalidomide and lenalidomide, and the first-in-its-class proteasome inhibitor bortezomib, has greatly improved clinical outcomes in patients with relapsed/refractory MM, but not all patients respond and those that do may eventually relapse or become refractory to treatment. The challenge is therefore to select the optimal treatment for each patient by balancing efficacy and toxicity. To do this, it is necessary to consider disease-related factors, such as the quality and duration of responses to previous therapies, and the aggressiveness of the relapse, and patient-related factors such as age, comorbidities, performance status, pre-existing toxicities and cytogenetic patterns. The message from the trials reviewed in this article is that the new agents may be used to re-treat relapsed/refractory disease, and that the sequencing of their administration should be modulated on the basis of the various disease and patient-related factors. Moreover, our understanding of the pharmacology and molecular action of the new drugs will contribute to the possibility of developing tailored treatment.
引用
收藏
页码:199 / 215
页数:17
相关论文
共 95 条
[1]   Treatment with lenalidomide does not appear to increase the risk of progression in lower risk myelodysplastic syndromes with 5q deletion. A comparative analysis by the Groupe Francophone des Myelodysplasies [J].
Ades, Lionel ;
Le Bras, Fabien ;
Sebert, Marie ;
Kelaidi, Charikleia ;
Lamy, Thierry ;
Dreyfus, Francois ;
Eclache, Virginie ;
Delaunay, Jacques ;
Bouscary, Didier ;
Visanica, Sorin ;
Turlure, Pascal ;
Bresler, Agnes Guerci ;
Cabrol, Marie-Paule ;
Banos, Anne ;
Blanc, Michel ;
Vey, Norbert ;
Delmer, Alain ;
Wattel, Eric ;
Chevret, Sylvie ;
Fenaux, Pierre .
HAEMATOLOGICA-THE HEMATOLOGY JOURNAL, 2012, 97 (02) :213-218
[2]   Monoclonal antibodies: potential new therapeutic treatment against multiple myeloma [J].
Allegra, Alessandro ;
Penna, Giuseppa ;
Alonci, Andrea ;
Russo, Sabina ;
Greve, Bruna ;
Innao, Vanessa ;
Minardi, Viviana ;
Musolino, Caterina .
EUROPEAN JOURNAL OF HAEMATOLOGY, 2013, 90 (06) :441-468
[3]   Thalidomide and dexamethasone for resistant multiple myeloma [J].
Anagnostopoulos, A ;
Weber, D ;
Rankin, K ;
Delasalle, K ;
Alexanian, R .
BRITISH JOURNAL OF HAEMATOLOGY, 2003, 121 (05) :768-771
[4]   Clinically relevant end points and new drug approvals for myeloma [J].
Anderson, K. C. ;
Kyle, R. A. ;
Rajkumar, S. V. ;
Stewart, A. K. ;
Weber, D. ;
Richardson, P. .
LEUKEMIA, 2008, 22 (02) :231-239
[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]   Thalidomide and thrombosis in multiple myeloma [J].
Barbui, T ;
Falanga, A .
JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2003, 1 (03) :421-422
[7]   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
[8]   Long-term pamidronate treatment of advanced multiple myeloma patients reduces skeletal events [J].
Berenson, JR ;
Lichtenstein, A ;
Porter, L ;
Dimopoulos, MA ;
Bordoni, R ;
George, S ;
Lipton, A ;
Keller, A ;
Ballester, O ;
Kovacs, M ;
Blacklock, H ;
Bell, R ;
Simeone, JF ;
Reitsma, DJ ;
Heffernan, M ;
Seaman, J ;
Knight, RD .
JOURNAL OF CLINICAL ONCOLOGY, 1998, 16 (02) :593-602
[9]   Improving overall survival and overcoming adverse prognosis in the treatment of cytogenetically high-risk multiple myeloma [J].
Bergsagel, P. Leif ;
Mateos, Maria-Victoria ;
Gutierrez, Norma C. ;
Rajkumar, S. Vincent ;
Miguel, Jesus F. San .
BLOOD, 2013, 121 (06) :884-892
[10]   Hematopoietic stem cell transplantation for multiple myeloma beyond 2010 [J].
Blade, Joan ;
Rosinol, Laura ;
Cibeira, Maria Teresa ;
Rovira, Montserrat ;
Carreras, Enric .
BLOOD, 2010, 115 (18) :3655-3663