Management of Newly Diagnosed Symptomatic Multiple Myeloma: updated Mayo Stratification of Myeloma and Risk-Adapted Therapy (mSMART) Consensus Guidelines

Multiple myeloma is a malignant plasma cell neoplasm that affects more than 20,000 people each year and is the second most common hematologic malignancy. It is part of a spectrum of monoclonal plasma cell disorders, many of which do not require active therapy. During the past decade, considerable pr...

Full description

Saved in:
Bibliographic Details
Published in:Mayo Clinic proceedings Vol. 84; no. 12; pp. 1095 - 1110
Main Authors: Kumar, Shaji K., MD, Mikhael, Joseph R., MD, Buadi, Francis K., MD, Dingli, David, MD, PhD, Dispenzieri, Angela, MD, Fonseca, Rafael, MD, Gertz, Morie A., MD, Greipp, Philip R., MD, Hayman, Suzanne R., MD, Kyle, Robert A., MD, Lacy, Martha Q., MD, Lust, John A., MD, PhD, Reeder, Craig B., MD, Roy, Vivek, MD, Russell, Stephen J., MD, PhD, Short, Kristen E. Detweiler, RN, CNP, Stewart, A. Keith, MD, Witzig, Thomas E., MD, Zeldenrust, Steven R., MD, PhD, Dalton, Robert J., MD, Rajkumar, S. Vincent, MD, Bergsagel, P. Leif, MD
Format: Journal Article Conference Proceeding
Language:English
Published: England Elsevier Inc 01-12-2009
Elsevier, Inc
Elsevier Limited
Mayo Foundation for Medical Education and Research
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Multiple myeloma is a malignant plasma cell neoplasm that affects more than 20,000 people each year and is the second most common hematologic malignancy. It is part of a spectrum of monoclonal plasma cell disorders, many of which do not require active therapy. During the past decade, considerable progress has been made in our understanding of the disease process and factors that influence outcome, along with development of new drugs that are highly effective in controlling the disease and prolonging survival without compromising quality of life. Identification of well-defined and reproducible prognostic factors and introduction of new therapies with unique modes of action and impact on disease outcome have for the first time opened up the opportunity to develop risk-adapted strategies for managing this disease. Although these risk-adapted strategies have not been prospectively validated, enough evidence can be gathered from existing randomized trials, subgroup analyses, and retrospective studies to develop a working framework. This set of recommendations represents such an effort—the development of a set of consensus guidelines by a group of experts to manage patients with newly diagnosed disease based on an interpretation of the best available evidence.
Bibliography:ObjectType-Article-1
ObjectType-Feature-2
content type line 25
ObjectType-News-3
SourceType-Conference Papers & Proceedings-1
ObjectType-Conference-4
Dr Kumar receives research support from Celgene, Novartis, Millennium Pharmaceuticals, Bayer, Genzyme, and Merck. Dr Mikhael receives research support from Celgene, Genentech, and Genzyme. Drs Dispenzieri, Roy, Stewart, Zeldenrust, and Rajkumar receive research support from Celgene. Dr Fonseca receives research support from Pfizer. Dr Gertz receives research support from Millennium Pharmaceuticals and Novartis. Dr Greipp receives research support from Celgene and Novartis and is on the Advisory Board for Amgen. Dr Hayman receives research support from Genentech. Dr Kyle serves on the Data Monitoring Committee for Johnson & Johnson and for Celgene. Dr Lacy receives research support from Pfizer and Millennium Pharmaceuticals. Dr Reeder receives research support from Celgene and Novartis. Dr Witzig receives research support from Celgene, Biogen-IDEC, and Novartis.
ISSN:0025-6196
1942-5546
DOI:10.4065/mcp.2009.0603