| |
|
|
|
|
|
|
|||
|
Blood, 12 November 2009, Vol. 114, No. 20, pp. 4369-4372. Prepublished online as a Blood First Edition Paper on September 15, 2009; DOI 10.1182/blood-2009-05-221689.
CLINICAL TRIALS AND OBSERVATIONS The persistence of immunophenotypically normal residual bone marrow plasma cells at diagnosis identifies a good prognostic subgroup of symptomatic multiple myeloma patients1 Hospital Universitario de Salamanca, Salamanca; 2 Centro de Investigación del Cáncer, Salamanca; 3 Hospital 12 de Octubre, Madrid; 4 Hospital Santa Creu I Sant Pau, Barcelona; 5 Hospital Clínico Universitario de Valladolid, Valladolid; 6 Complejo Hospitalario de León, León; 7 Hospital General de Castellón, Castellón; 8 Hospital del Bierzo, Ponferrada; 9 Hospital General de Segovia, Segovia; 10 Hospital Lozano Blesa, Zaragoza; 11 Hospital Central de Asturias, Oviedo; 12 Clínico San Carlos, Madrid; 13 Hospital La Fe, Valencia; 14 Hospital Virgen de la Concha, Zamora; 15 Hospital Dr. Josep Trueta, Gerona; 16 Hospital Clínic, Institut d'Investigacions Biomèdiques August Pi i Sunyer Barcelona, Barcelona; and 17 Servicio General de Citometría, Universidad de Salamanca, Salamanca, Spain
Multiparameter flow cytometry immunophenotyping allows discrimination between normal (N-) and myelomatous (MM-) plasma cells (PCs) within the bone marrow plasma cell compartment (BMPCs). Here we report on the prognostic relevance of detecting more than 5% residual normal plasma cells from all bone marrow plasma cells (N-PCs/BMPCs) by multiparameter flow cytometry in a series of 594 newly diagnosed symptomatic MM patients, uniformly treated according to the Grupo Español de MM 2000 (GEM2000) protocol. Our results show that symptomatic MM patients with more than 5% N-PCs/BMPCs (n = 80 of 594; 14%) have a favorable baseline clinical prospect, together with a significantly lower frequency of high-risk cytogenetic abnormalities and higher response rates. Moreover, this group of patients had a significantly longer progression-free survival (median, 54 vs 42 months, P = .001) and overall survival (median, not reached vs 89 months, P = .04) than patients with less than or equal to 5% N-PCs/BMPCs. Our findings support the clinical value of detecting residual normal PCs in MM patients at diagnosis because this reveals a good prognostic category that could benefit from specific therapeutic approaches. This trial was registered at www.clinicaltrials.gov as NCT00560053 [ClinicalTrials.gov] .
| |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Copyright © 2009 by American Society of Hematology Online ISSN: 1528-0020 | |||||||||