Abnormalities in Chromosomes 1q and 13 Independently Correlate With Factors of Poor Prognosis in Multiple Myeloma.
10.3343/alm.2016.36.6.573
- Author:
Miyoung KIM
1
;
Young Su JU
;
Eun Jin LEE
;
Hee Jung KANG
;
Han Sung KIM
;
Hyoun Chan CHO
;
Hyo Jung KIM
;
Jung Ah KIM
;
Dong Soon LEE
;
Young Kyung LEE
Author Information
1. Department of Laboratory Medicine, Hallym University College of Medicine, Anyang, Korea. lyoungk@hallym.or.kr
- Publication Type:Original Article
- Keywords:
Myeloma;
Chromosome;
Prognosis
- MeSH:
Adolescent;
Adult;
Aged;
Aged, 80 and over;
Calcium/blood;
*Chromosome Aberrations;
Chromosomes, Human, Pair 1;
Chromosomes, Human, Pair 13;
Chromosomes, Human, Pair 4;
Creatine/blood;
Female;
Hemoglobins/analysis;
Humans;
Immunoglobulin A/blood;
Immunoglobulin G/blood;
Karyotyping;
Male;
Middle Aged;
Multiple Myeloma/*diagnosis/genetics/mortality;
Multivariate Analysis;
Prognosis;
Survival Rate;
Young Adult
- From:Annals of Laboratory Medicine
2016;36(6):573-582
- CountryRepublic of Korea
- Language:English
-
Abstract:
BACKGROUND: We comprehensively profiled cytogenetic abnormalities in multiple myeloma (MM) and analyzed the relationship between cytogenetic abnormalities of undetermined prognostic significance and established prognostic factors. METHODS: The karyotype of 333 newly diagnosed MM cases was analyzed in association with established prognostic factors. Survival analysis was also performed. RESULTS: MM with abnormal karyotypes (41.1%) exhibited high international scoring system (ISS) stage, frequent IgA type, elevated IgG or IgA levels, elevated calcium levels, elevated creatine (Cr) levels, elevated β2-microglobulin levels, and decreased Hb levels. Structural abnormalities in chromosomes 1q, 4, and 13 were independently associated with elevated levels of IgG or IgA, calcium, and Cr, respectively. Chromosome 13 abnormalities were associated with poor prognosis and decreased overall survival. CONCLUSIONS: This is the first study to demonstrate that abnormalities in chromosomes 1q, 4, and 13 are associated with established factors for poor prognosis, irrespective of the presence of other concurrent chromosomal abnormalities. Chromosome 13 abnormalities have a prognostic impact on overall survival in association with elevated Cr levels. Frequent centromeric breakpoints appear to be related to MM pathogenesis.
