Literature DB >> 16506632

New treatments for multiple myeloma.

Paul G Richardson1, Robert Schlossman, Teru Hideshima, Kenneth C Anderson.   

Abstract

In 2004, multiple myeloma was diagnosed in more than 15,000 people in the United States and will account for approximately 20% of deaths due to hematologic malignancies. Although traditional therapies such as melphalan (Alkeran)/prednisone, combination chemotherapy with VAD (vincristine, doxorubicin [Adriamycin], and dexamethasone), and high-dose chemotherapy with stem cell transplantation have shown some success, median survival remains between 3 to 5 years. Treatment options for patients with multiple myeloma have increased in recent years, with the promise of improvement in survival. New agents, such as the proteasome inhibitor bortezomib (Velcade), the antiangiogenic and immunomodulator thalidomide (Thalomid) and its analogs, such as lenalidomide (Revlimid), together with other small molecules, including arsenic trioxide (Trisenox), and other targeted therapies, have been studied alone and in combination with other antineoplastic therapies, either as induction therapy prior to stem cell transplantation or in patients with relapsed disease. Bortezomib recently was approved in the United States for the treatment of multiple myeloma in patients who have received at least one prior therapy. The use of bortezomib-based regimens as front-line therapy as well as the use of other agents in multiple myeloma remain under investigation, and approvals for both thalidomide and lenalidomide are hoped for soon, with the overall prospect of patient outcome continuing to be increasingly positive.

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Year:  2005        PMID: 16506632

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


  13 in total

1.  Evidence of a role for activation of Wnt/beta-catenin signaling in the resistance of plasma cells to lenalidomide.

Authors:  Chad C Bjorklund; Wencai Ma; Zhi-Qiang Wang; R Eric Davis; Deborah J Kuhn; Steven M Kornblau; Michael Wang; Jatin J Shah; Robert Z Orlowski
Journal:  J Biol Chem       Date:  2010-12-28       Impact factor: 5.157

2.  In Silico Modeling-based Identification of Glucose Transporter 4 (GLUT4)-selective Inhibitors for Cancer Therapy.

Authors:  Rama K Mishra; Changyong Wei; Richard C Hresko; Richa Bajpai; Monique Heitmeier; Shannon M Matulis; Ajay K Nooka; Steven T Rosen; Paul W Hruz; Gary E Schiltz; Mala Shanmugam
Journal:  J Biol Chem       Date:  2015-04-06       Impact factor: 5.157

3.  Development of GLUT4-selective antagonists for multiple myeloma therapy.

Authors:  Changyong Wei; Richa Bajpai; Horrick Sharma; Monique Heitmeier; Atul D Jain; Shannon M Matulis; Ajay K Nooka; Rama K Mishra; Paul W Hruz; Gary E Schiltz; Mala Shanmugam
Journal:  Eur J Med Chem       Date:  2017-08-14       Impact factor: 6.514

Review 4.  Management of paraproteinaemia.

Authors:  Lucy Cook; Donald H C Macdonald
Journal:  Postgrad Med J       Date:  2007-04       Impact factor: 2.401

5.  Multiple myeloma exhibits novel dependence on GLUT4, GLUT8, and GLUT11: implications for glucose transporter-directed therapy.

Authors:  Samuel K McBrayer; Javelin C Cheng; Seema Singhal; Nancy L Krett; Steven T Rosen; Mala Shanmugam
Journal:  Blood       Date:  2012-03-27       Impact factor: 22.113

6.  Targeting the metabolic plasticity of multiple myeloma with FDA-approved ritonavir and metformin.

Authors:  Sevim Dalva-Aydemir; Richa Bajpai; Maylyn Martinez; Kehinde U A Adekola; Irawati Kandela; Changyong Wei; Seema Singhal; Jennifer E Koblinski; Noopur S Raje; Steven T Rosen; Mala Shanmugam
Journal:  Clin Cancer Res       Date:  2014-12-26       Impact factor: 12.531

7.  Tumor cell gene expression changes following short-term in vivo exposure to single agent chemotherapeutics are related to survival in multiple myeloma.

Authors:  Bart Burington; Bart Barlogie; Fenghuang Zhan; John Crowley; John D Shaughnessy
Journal:  Clin Cancer Res       Date:  2008-08-01       Impact factor: 12.531

8.  Proteasomal inhibition stabilizes topoisomerase IIalpha protein and reverses resistance to the topoisomerase II poison ethonafide (AMP-53, 6-ethoxyazonafide).

Authors:  Lauren M Congdon; Alan Pourpak; Aluvia M Escalante; Robert T Dorr; Terry H Landowski
Journal:  Biochem Pharmacol       Date:  2007-11-04       Impact factor: 5.858

9.  Targeting glucose consumption and autophagy in myeloma with the novel nucleoside analogue 8-aminoadenosine.

Authors:  Mala Shanmugam; Samuel K McBrayer; Jun Qian; Kiril Raikoff; Michael J Avram; Seema Singhal; Varsha Gandhi; Paul T Schumacker; Nancy L Krett; Steven T Rosen
Journal:  J Biol Chem       Date:  2009-07-31       Impact factor: 5.157

10.  A novel insertion ins(18;5)(q21.1;q31.2q35.1) in acute myeloid leukemia associated with microdeletions at 5q31.2, 5q35.1q35.2 and 18q12.3q21.1 detected by oligobased array comparative genomic hybridization.

Authors:  Eigil Kjeldsen
Journal:  Mol Cytogenet       Date:  2014-09-25       Impact factor: 2.009

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