| Literature DB >> 23860448 |
N Puig1, M E Sarasquete1, A Balanzategui1, J Martínez2, B Paiva1, H García1, S Fumero1, C Jiménez1, M Alcoceba1, M C Chillón1, E Sebastián1, L Marín1, M A Montalbán2, M V Mateos1, A Oriol3, L Palomera4, J de la Rubia5, M B Vidriales1, J Bladé6, J J Lahuerta2, M González1, J F S Miguel1, R García-Sanz1.
Abstract
We have analyzed the applicability, sensitivity and prognostic value of allele-specific oligonucleotide real-time quantitative PCR (ASO RQ-PCR) as a method for minimal residual disease (MRD) assessment in patients with multiple myeloma (MM), comparing the results with those of multiparameter flow cytometry (MFC). A total of 170 patients enrolled in three consecutive Spanish trials achieving at least partial response after treatment were included. Lack of clonality detection (n=31), unsuccessful sequencing (n=17) and suboptimal ASO performance (n=51) limited the applicability of PCR to 42% of cases. MRD was finally investigated in 103 patients (including 32 previously studied) with persistent disease identified by PCR and MFC in 54% and 46% of cases, respectively. A significant correlation in MRD quantitation by both the techniques was noted (r=0.881, P<0.001), being reflective of treatment intensity. Patients with <10(-4) residual tumor cells showed longer progression-free survival (PFS) compared with the rest (not reached (NR) vs 31 months, P=0.002), with similar results observed with MFC. Among complete responders (n=62), PCR discriminated two risk groups with different PFS (49 vs 26 months, P=0.001) and overall survival (NR vs 60 months, P=0.008). Thus, although less applicable than MFC, ASO RQ-PCR is a powerful technique to assess treatment efficacy and risk stratification in MM.Entities:
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Year: 2013 PMID: 23860448 DOI: 10.1038/leu.2013.217
Source DB: PubMed Journal: Leukemia ISSN: 0887-6924 Impact factor: 11.528