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Consensus recommendations for risk stratification in multiple myeloma: report of the International Myeloma Workshop Consensus Panel 2

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MUNSHI Nikhil C. ANDERSON Kenneth C. BERGSAGEL P. Leif SHAUGHNESSY John PALUMBO Antonio DURIE Brian FONSECA Rafael STEWART A. Keith HAROUSSEAU Jean-Luc DIMOPOULOS Meletios JAGANNATH Sundar HÁJEK Roman SEZER Orhan KYLE Robert SONNEVELD Pieter CAVO Michele RAJKUMAR M. SAN MIGUEL J. CROWLEY J. AVET-LOISEAU Hervé

Rok publikování 2011
Druh Článek v odborném periodiku
Časopis / Zdroj Blood
Fakulta / Pracoviště MU

Lékařská fakulta

Citace
Doi http://dx.doi.org/10.1182/blood-2010-10-300970
Obor Onkologie a hematologie
Klíčová slova multiple myeloma; stratification;risk factor
Popis A panel of members of the 2009 International Myeloma Workshop developed guidelines for risk stratification in multiple myeloma. The purpose of risk stratification is not to decide time of therapy but to prognosticate. There is general consensus that risk stratification is applicable to newly diagnosed patients; however, some genetic abnormalities characteristic of poor outcome at diagnosis may suggest poor outcome if only detected at the time of relapse. Thus, in good-risk patients, it is necessary to evaluate for high-risk features at relapse. Although detection of any cytogenetic abnormality is considered to suggest higher-risk disease, the specific abnormalities considered as poor risk are cytogenetically detected chromosomal 13 or 13q deletion, t(4;14) and del17p, and detection by fluorescence in situ hybridization of t(4;14), t(14;16), and del17p. Detection of 13q deletion by fluorescence in situ hybridization only, in absence of other abnormalities, is not considered a high-risk feature. High serum beta(2)-microglobulin level and International Staging System stages II and III, incorporating high beta(2)-microglobulin and low albumin, are considered to predict higher risk disease. There was a consensus that the high-risk features will change in the future, with introduction of other new agents or possibly new combinations.

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