Literature DB >> 17722741

Novel therapeutic avenues in myeloma: changing the treatment paradigm.

Joanne Ghobrial1, Irene M Ghobrial, Constantine Mitsiades, Xavier Leleu, Evdoxia Hatjiharissi, Anne-Sophie Moreau, Aldo Roccaro, Robert Schlossman, Teru Hideshima, Kenneth C Anderson, Paul Richardson.   

Abstract

Our better understanding of the complex interaction of multiple myeloma (MM) cells with their bone marrow microenvironment and the signaling pathways that are dysregulated in this process has resulted in a dramatic increase in the therapeutic agents available for this disease. A number of these new agents have demonstrated significant activity in patients with MM. Over the past 5 years, three drugs have received approval from the US Food and Drug Administration for therapy in MM--bortezomib, thalidomide, and lenalidomide. To date, the choice of therapy for MM is not individualized according to the biologic characteristics of the disease, but future studies should enable us to identify patients who may benefit most from certain therapeutic interventions, and thus develop individualized therapy for MM. In this review, we will present some of the treatment algorithms currently developed for patients with MM and focus on established advances in therapy, specifically with thalidomide, bortezomib, and lenalidomide. We will also discuss some of the emerging novel therapeutic agents showing promise in phase I/II clinical trials in MM.

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Year:  2007        PMID: 17722741

Source DB:  PubMed          Journal:  Oncology (Williston Park)        ISSN: 0890-9091            Impact factor:   2.990


  6 in total

Review 1.  The tumor microenvironment shapes hallmarks of mature B-cell malignancies.

Authors:  K H Shain; W S Dalton; J Tao
Journal:  Oncogene       Date:  2015-02-02       Impact factor: 9.867

2.  Peripheral neuropathy associated with novel therapies in patients with multiple myeloma: consensus statement of the IMF Nurse Leadership Board.

Authors:  Joseph D Tariman; Ginger Love; Emily McCullagh; Stacey Sandifer
Journal:  Clin J Oncol Nurs       Date:  2008-06       Impact factor: 1.027

3.  Proteasome inhibition causes regression of leukemia and abrogates BCR-ABL-induced evasion of apoptosis in part through regulation of forkhead tumor suppressors.

Authors:  Zainab Jagani; Keli Song; Jeffery L Kutok; M Rajan Dewar; Armelle Melet; Tanya Santos; Alexandra Grassian; Saghi Ghaffari; Catherine Wu; Heather Yeckes-Rodin; Heather Yeckes Rodin; Ruibao Ren; Kenneth Miller; Roya Khosravi-Far
Journal:  Cancer Res       Date:  2009-08-04       Impact factor: 12.701

4.  Management of side effects of novel therapies for multiple myeloma: consensus statements developed by the International Myeloma Foundation's Nurse Leadership Board.

Authors:  Page Bertolotti; Elizabeth Bilotti; Kathleen Colson; Kathleen Curran; Deborah Doss; Beth Faiman; Maria Gavino; Bonnie Jenkins; Kathy Lilleby; Ginger Love; Patricia A Mangan; Emily McCullagh; Teresa Miceli; Kena Miller; Kathryn Rogers; Sandra Rome; Stacey Sandifer; Lisa C Smith; Joseph D Tariman; Jeanne Westphal
Journal:  Clin J Oncol Nurs       Date:  2008-06       Impact factor: 1.027

5.  The novel polyamine analogue CGC-11093 enhances the antimyeloma activity of bortezomib.

Authors:  Jennifer S Carew; Steffan T Nawrocki; Venudhar K Reddy; Dorothy Bush; Jerold E Rehg; Andrew Goodwin; Janet A Houghton; Robert A Casero; Laurence J Marton; John L Cleveland
Journal:  Cancer Res       Date:  2008-06-15       Impact factor: 12.701

6.  Waldenstrom macroglobulinemia.

Authors:  Xavier Leleu; Aldo M Roccaro; Anne-Sophie Moreau; Sophie Dupire; Daniela Robu; Julie Gay; Evdoxia Hatjiharissi; Nicholas Burwik; Irene M Ghobrial
Journal:  Cancer Lett       Date:  2008-06-13       Impact factor: 8.679

  6 in total

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