Abstract
The clinical efficacy of evaluating genetic anomalies in metaphase cells versus interphase nuclei for multiple myeloma (MM) is poorly understood. Therefore, survival for 154 patients with newly diagnosed untreated MM was compared with results from analysis of metaphase and interphase cells. Metaphases were studied by conventional cytogenetics and fluorescent-labeled DNA probes (fluorescence in situ hybridization [FISH]), whereas inter-phase nuclei were evaluated only by FISH. All FISH studies were done using DNA probes to detect t(4;14)(p16;q32), t(11;14)(q13;q32), t(14;16)(q32;q23), del(17) (p13.1), and chromosome 13 anomalies. Metaphases were abnormal by cytogenetics and/or metaphase FISH in 61 (40%) patients. Abnormal interphase nuclei were observed in 133 (86%) patients, including each patient with abnormal metaphases. FISH was a necessary adjunct to cytogenetics to detect t(4;14) and t(14;16) in metaphase cells. Patient survival was especially poor for patients with greater than 50% abnormal interphase nuclei, although this result was more likely due to level of plasma cells than specific chromosome anomalies. For metaphase data, patients with t(4;14), t(14;16), del(17) (p13.1), and/or chromosome 13 anomalies (primarily monosomy 13) had poor survival. A different outcome was observed for interphase data as patients with t(4;14) or t(14;16) had poor survival, whereas patients with chromosome 13 anomalies had intermediate survival: interphase FISH did not substitute for metaphase analysis.
MeSH Terms
Adult
Aged
Aged, 80 and over
Chromosome Aberrations
Chromosomes, Human/genetics
Disease-Free Survival
Female
Humans
In Situ Hybridization, Fluorescence/methods
Interphase/genetics
Male
Metaphase/genetics
Middle Aged
Multiple Myeloma/diagnosis,genetics,mortality
Predictive Value of Tests
Authors & Affiliations
12 authors, click to expand affiliations / ORCID
Dewald Gordon W
Cytogenetics Laboratory, Mayo Clinic, Rochester, MN 55905, USA. gdewald@mayo.edu
Therneau Terry
Larson Dirk
Lee You Kyoung
Fink Stephanie
Smoley Stephanie
Paternoster Sarah
Adeyinka Adewale
Ketterling Rhett
Van Dyke Daniel L
Fonseca Rafael
Kyle Robert
References (21)
21 references, click to expand
-
Clinical and biologic implications of recurrent genomic aberrations in myeloma.
Blood. 2003 Jun 1;101(11):4569-75
PMID: 12576322
-
Chromosome abnormalities clustering and its implications for pathogenesis and prognosis in myeloma.
Leukemia. 2003 Feb;17(2):427-36
PMID: 12592343
-
Combined cytogenetic testing and fluorescence in situ hybridization analysis in the study of chronic lymphocytic leukemia and multiple myeloma.
Cancer Genet Cytogenet. 2004 Aug;153(1):73-6
PMID: 15325099
-
The clinical significance of cytogenetic studies in 100 patients with multiple myeloma, plasma cell leukemia, or amyloidosis.
Blood. 1985 Aug;66(2):380-90
PMID: 3926026
-
The efficacy of direct, 24-hour culture, and mitotic synchronization methods for cytogenetic analysis of bone marrow in neoplastic hematologic disorders.
Cancer Genet Cytogenet. 1985 Sep;18(1):1-10
PMID: 4027947
-
Unbalanced 1;7 translocation and therapy-induced hematologic disorders: a possible relationship.
Am J Hematol. 1986 Jan;21(1):39-47
PMID: 3706288
-
Cytogenetic findings in 200 patients with multiple myeloma.
Cancer Genet Cytogenet. 1995 Jul 1;82(1):41-9
PMID: 7627933
-
Multiple myeloma: high incidence of chromosomal aneuploidy as detected by interphase fluorescence in situ hybridization.
Cancer Res. 1995 Sep 1;55(17):3854-9
PMID: 7641204
-
Poor prognosis in multiple myeloma is associated only with partial or complete deletions of chromosome 13 or abnormalities involving 11q and not with other karyotype abnormalities.
Blood. 1995 Dec 1;86(11):4250-6
PMID: 7492784
-
Multiple myeloma: almost all patients are cytogenetically abnormal.
Br J Haematol. 1996 Aug;94(2):217-27
PMID: 8759879
-
A novel three-color, clone-specific fluorescence in situ hybridization procedure for monoclonal gammopathies.
Cancer Genet Cytogenet. 1998 Feb;101(1):7-11
PMID: 9460493
-
Highly sensitive fluorescence in situ hybridization method to detect double BCR/ABL fusion and monitor response to therapy in chronic myeloid leukemia.
Blood. 1998 May 1;91(9):3357-65
PMID: 9558393
-
Ploidy, as detected by fluorescence in situ hybridization, defines different subgroups in multiple myeloma.
Leukemia. 2005 Feb;19(2):275-8
PMID: 15538401
-
Genetic heterogeneity in multiple myeloma.
Leukemia. 2005 Feb;19(2):191-4
PMID: 15538406
-
Both chromosome 13 abnormalities by metaphase cytogenetics and deletion of 13q by interphase FISH only are prognostically relevant in multiple myeloma.
Eur J Haematol. 2003 Sep;71(3):179-83
PMID: 12930318
-
Correlation between cytogenetic abnormalities and disease characteristics in multiple myeloma: monosomy of chromosome 13 and structural abnormalities of 11q are associated with a high percentage of S-phase plasma cells.
Haematologica. 2000 Nov;85(11):1146-52
PMID: 11064466
-
Chromosome 13 abnormalities in multiple myeloma are mostly monosomy 13.
Br J Haematol. 2000 Dec;111(4):1116-7
PMID: 11227093
-
The t(4;14)(p16.3;q32) is strongly associated with chromosome 13 abnormalities in both multiple myeloma and monoclonal gammopathy of undetermined significance.
Blood. 2001 Aug 15;98(4):1271-2
PMID: 11510469
-
Biological and prognostic significance of interphase fluorescence in situ hybridization detection of chromosome 13 abnormalities (delta13) in multiple myeloma: an eastern cooperative oncology group study.
Cancer Res. 2002 Feb 1;62(3):715-20
PMID: 11830525
-
Oncogenesis of multiple myeloma: 14q32 and 13q chromosomal abnormalities are not randomly distributed, but correlate with natural history, immunological features, and clinical presentation.
Blood. 2002 Mar 15;99(6):2185-91
PMID: 11877296
-
Genetics and cytogenetics of multiple myeloma: a workshop report.
Cancer Res. 2004 Feb 15;64(4):1546-58
PMID: 14989251