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Prognostic significance of copy-number alterations in multiple myeloma.


ABSTRACT:

Purpose

Chromosomal aberrations are a hallmark of multiple myeloma but their global prognostic impact is largely unknown.

Patients and methods

We performed a genome-wide analysis of malignant plasma cells from 192 newly diagnosed patients with myeloma using high-density, single-nucleotide polymorphism (SNP) arrays to identify genetic lesions associated with prognosis.

Results

Our analyses revealed deletions and amplifications in 98% of patients. Amplifications in 1q and deletions in 1p, 12p, 14q, 16q, and 22q were the most frequent lesions associated with adverse prognosis, whereas recurrent amplifications of chromosomes 5, 9, 11, 15, and 19 conferred a favorable prognosis. Multivariate analysis retained three independent lesions: amp(1q23.3), amp(5q31.3), and del(12p13.31). When adjusted to the established prognostic variables (ie, t(4;14), del(17p), and serum beta(2)-microglobulin [Sbeta(2)M]), del(12p13.31) remained the most powerful independent adverse marker (P < .0001; hazard ratio [HR], 3.17) followed by Sbeta(2)M (P < .0001; HR, 2.78) and the favorable marker amp(5q31.3) (P = .0005; HR, 0.37). Patients with amp(5q31.3) alone and low Sbeta(2)M had an excellent prognosis (5-year overall survival, 87%); conversely, patients with del(12p13.31) alone or amp(5q31.3) and del(12p13.31) and high Sbeta(2)M had a very poor outcome (5-year overall survival, 20%). This prognostic model was validated in an independent validation cohort of 273 patients with myeloma.

Conclusion

These findings demonstrate the power and accessibility of molecular karyotyping to predict outcome in myeloma. In addition, integration of expression of genes residing in the lesions of interest revealed putative features of the disease driving short survival.

SUBMITTER: Avet-Loiseau H 

PROVIDER: S-EPMC2754906 | biostudies-literature | 2009 Sep

REPOSITORIES: biostudies-literature

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Prognostic significance of copy-number alterations in multiple myeloma.

Avet-Loiseau Hervé H   Li Cheng C   Magrangeas Florence F   Gouraud Wilfried W   Charbonnel Catherine C   Harousseau Jean-Luc JL   Attal Michel M   Marit Gerald G   Mathiot Claire C   Facon Thierry T   Moreau Philippe P   Anderson Kenneth C KC   Campion Loïc L   Munshi Nikhil C NC   Minvielle Stéphane S  

Journal of clinical oncology : official journal of the American Society of Clinical Oncology 20090817 27


<h4>Purpose</h4>Chromosomal aberrations are a hallmark of multiple myeloma but their global prognostic impact is largely unknown.<h4>Patients and methods</h4>We performed a genome-wide analysis of malignant plasma cells from 192 newly diagnosed patients with myeloma using high-density, single-nucleotide polymorphism (SNP) arrays to identify genetic lesions associated with prognosis.<h4>Results</h4>Our analyses revealed deletions and amplifications in 98% of patients. Amplifications in 1q and del  ...[more]

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