Multiple Myeloma — Recent Developments in Molecular and Cellular Biology

Author(s):  
B. Barlogie ◽  
R. Hoover ◽  
J. Epstein
Author(s):  
Philippe Moreau ◽  
Cyrille Touzeau

Recent developments in the treatment of multiple myeloma (MM) have led to improvements in response rates and to increased survival. A major advance in the last decade has been the introduction of the novel agents thalidomide, bortezomib, and lenalidomide as part of front-line treatment in both the transplant and nontransplant settings. However, disease relapse is inevitable for the majority of patients and myeloma typically recurs more aggressively with each relapse, eventually leading to the development of treatment-refractory disease. Several phase II and III trials have demonstrated the efficacy of recently approved agents in the setting of relapsed and relapsed and refractory MM, including pomalidomide and carfilzomib. Ixazomib, an oral proteasome inhibitor, and multiple other novel classes of agents are being investigated. These include monoclonal antibodies and histone deacetylase inhibitors, which may further add to the therapeutic armamentarium for this malignancy. Therefore, in a disease characterized by multiple relapses, the optimal sequencing of the different effective options is an important consideration in attempting to prolong survival.


2020 ◽  
Vol 21 (21) ◽  
pp. 8192
Author(s):  
Mattia D’Agostino ◽  
Salvatore Innorcia ◽  
Mario Boccadoro ◽  
Sara Bringhen

Immunotherapy is increasingly used in the treatment of multiple myeloma (MM). Monoclonal antibodies (mAbs) are safe and effective ways to elicit immunotherapeutic responses. In 2015, daratumumab has become the first mAb approved by the Food and Drug Administration for clinical use in MM and, in the last 5 years, a lot of clinical and preclinical research has been done to optimize the use of this drug class. Currently, mAbs have already become part of standard-of-care combinations for the treatment of relapsed/refractory MM and very soon they will also be used in the frontline setting. The success of simple mAbs (‘naked mAbs’) prompted the development of new types of molecules. Antibody–drug conjugates (ADCs) are tumor-targeting mAbs that release a cytotoxic payload into the tumor cells upon antigen binding in order to destroy them. Bispecific antibodies (BiAbs) are mAbs simultaneously targeting a tumor-associated antigen and an immune cell-associated antigen in order to redirect the immune cell cytotoxicity against the tumor cell. These different constructs produced solid preclinical data and promising clinical data in phase I/II trials. The aim of this review article is to summarize all the recent developments in the field, including data on naked mAbs, ADCs and BiAbs.


2008 ◽  
Vol 1138 (1) ◽  
pp. 19-21 ◽  
Author(s):  
Antonio Palumbo ◽  
Valeria Magarotto ◽  
Francesca Gay ◽  
Patrizia Falco ◽  
Sara Bringhen ◽  
...  

2003 ◽  
Vol 18 (4) ◽  
pp. 497-511 ◽  
Author(s):  
Diely Pichardo ◽  
Seema Singhal ◽  
Jayesh Mehta ◽  
Steven Rosen

2016 ◽  
Vol 157 (4) ◽  
pp. 123-137
Author(s):  
Gergely Varga ◽  
Gábor Mikala ◽  
László Váróczy ◽  
Árpád Illés

The last decade has witnessed a dramatic progress in the treatment of multiple myeloma. Both the chemotherapy protocols and the supportive therapy options have improved significantly since the publication of the previous Hungarian national guideline. An increasing proportion of patients now reach a durable response and cure became a potential option for some. The aim of the authors was to adapt the international guidelines to the specific circumstances of the Hungarian healthcare system in the light of the most recent developments. Orv. Hetil., 2016, 157(4), 123–137.


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