Support is requested for an integrated clinical-therapeutic and laboratory research program on GROWTH CONTROL OF MULTIPLE MYELOMA by a team of experienced investigators, most of whom have interacted closely for several years and have independent research support. The clinical Project I emphasizes a curative approach for newly diagnosed patients through dose-intensive cytotoxic chemotherapy requiring hemopoietic growth factor and stem cell support (""""""""Total Therapy""""""""). In addition, biological agents with the potential of exerting direct antitumor effect or activating and augmenting normal host-defense mechanisms (T and NK cells) will be evaluated in previously treated patients. In order to take advantage of the large patient population seen at our Center with this rare malignancy and related disorders, a comprehensive workup will be performed of cytogenetics, molecular genetics and cytokines. the derived Myeloma Data Base should prove useful for a deeper understanding of etiology, disease manifestations and progression. the clinical project and the associated Cores (Chromosome and Molecular Genetics; Cytokines; Data Management) will provide a cohesive framework for specific basic laboratory research projects examining the intricate cytokine network involved in myeloma growth and clinical symptoms manifestation (Project II); the molecular mechanisms of dexamethasone activity and resistance (Project III); as well as the growth-controlling contributions of autoreactive cells shedding immunoglobulin binding factor (CD16) (Project IV). These host cells may be subject to therapeutic manipulations by biological events investigated in Project I, mainly dexamethasone, IL-4, ivIg, interferons and all-trans-retinoic acid.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Program Projects (P01)
Project #
5P01CA055819-02
Application #
2096929
Study Section
Special Emphasis Panel (SRC (K2))
Project Start
1993-02-15
Project End
1996-01-31
Budget Start
1994-02-01
Budget End
1995-01-31
Support Year
2
Fiscal Year
1994
Total Cost
Indirect Cost
Name
University of Arkansas for Medical Sciences
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
City
Little Rock
State
AR
Country
United States
Zip Code
72205
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Went, Molly; Sud, Amit; Försti, Asta et al. (2018) Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma. Nat Commun 9:3707
Mehdi, Syed J; Johnson, Sarah K; Epstein, Joshua et al. (2018) Mesenchymal stem cells gene signature in high-risk myeloma bone marrow linked to suppression of distinct IGFBP2-expressing small adipocytes. Br J Haematol :
Rasche, Leo; Angtuaco, Edgardo J; Alpe, Terri L et al. (2018) The presence of large focal lesions is a strong independent prognostic factor in multiple myeloma. Blood 132:59-66
Went, M; Sud, A; Law, P J et al. (2017) Assessing the effect of obesity-related traits on multiple myeloma using a Mendelian randomisation approach. Blood Cancer J 7:e573
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Rasche, Leo; Weinhold, Niels; Morgan, Gareth J et al. (2017) Immunologic approaches for the treatment of multiple myeloma. Cancer Treat Rev 55:190-199
Rasche, L; Chavan, S S; Stephens, O W et al. (2017) Spatial genomic heterogeneity in multiple myeloma revealed by multi-region sequencing. Nat Commun 8:268
Jethava, Yogesh S; Mitchell, Alan; Epstein, Joshua et al. (2017) Adverse Metaphase Cytogenetics Can Be Overcome by Adding Bortezomib and Thalidomide to Fractionated Melphalan Transplants. Clin Cancer Res 23:2665-2672
Schinke, Carolina; Hoering, Antje; Wang, Hongwei et al. (2017) The prognostic value of the depth of response in multiple myeloma depends on the time of assessment, risk status and molecular subtype. Haematologica 102:e313-e316

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