Abstract
This report represents a further update of the consensus panel criteria for the assessment of clinical response in patients with Waldenström macroglobulinaemia (WM). These criteria have been updated in light of further data demonstrating an improvement in categorical responses with new drug regimens as well as acknowledgement of the fact that such responses are predictive of overall outcome. A number of key changes are proposed but challenges do however remain and these include the variability in kinetics of immunoglobulin M (IgM) reduction with different treatment modalities and the apparent discrepancy between IgM and bone marrow/tissue response noted with some regimens. Planned sequential bone marrow assessments are encouraged in clinical trials.
© 2012 Blackwell Publishing Ltd.
Publication types
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Consensus Development Conference
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Practice Guideline
MeSH terms
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Antibodies, Monoclonal / blood
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Antibodies, Monoclonal / therapeutic use
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Antimetabolites / therapeutic use
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Bone Marrow Examination / methods
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Bone Marrow Examination / standards
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Boronic Acids / therapeutic use
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Bortezomib
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Densitometry
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Disease Progression
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Disease-Free Survival
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Forecasting
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Hematopoiesis
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Humans
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Immunoglobulin Light Chains / blood
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Immunoglobulin M / blood
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Immunosuppressive Agents / therapeutic use
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Neoplasm, Residual
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Nephelometry and Turbidimetry
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Positron-Emission Tomography
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Pyrazines / therapeutic use
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Remission Induction
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Survival Analysis
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Tomography, X-Ray Computed
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Treatment Outcome
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Waldenstrom Macroglobulinemia / blood
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Waldenstrom Macroglobulinemia / drug therapy*
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Waldenstrom Macroglobulinemia / pathology
Substances
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Antibodies, Monoclonal
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Antimetabolites
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Boronic Acids
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Immunoglobulin Light Chains
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Immunoglobulin M
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Immunosuppressive Agents
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Pyrazines
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Bortezomib