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Cytogenetic Abnormalities in Multiple Myeloma Patients at a Tertiary Healthcare Center in India

OBJECTIVE: Multiple myeloma (MM) is a clinically and genetically heterogeneous plasma cell neoplasm. The prognosis of MM patients is dependent on several factors including the patient’s age, the stage of disease and genetic alterations. This study aimed to determine the frequency of common chromosom...

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Autores principales: Govindasamy, Perumal, Pandurangan, Prabu, Tarigopula, Anil, Mani, Rama, Samuel, Chandra R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: West Asia Organization for Cancer Prevention 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6485553/
https://www.ncbi.nlm.nih.gov/pubmed/30678438
http://dx.doi.org/10.31557/APJCP.2019.20.1.235
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author Govindasamy, Perumal
Pandurangan, Prabu
Tarigopula, Anil
Mani, Rama
Samuel, Chandra R
author_facet Govindasamy, Perumal
Pandurangan, Prabu
Tarigopula, Anil
Mani, Rama
Samuel, Chandra R
author_sort Govindasamy, Perumal
collection PubMed
description OBJECTIVE: Multiple myeloma (MM) is a clinically and genetically heterogeneous plasma cell neoplasm. The prognosis of MM patients is dependent on several factors including the patient’s age, the stage of disease and genetic alterations. This study aimed to determine the frequency of common chromosomal abnormalities and their significance in MM patients referred to a tertiary healthcare center in India. METHODS: Fluorescence in situ hybridization on interphase nuclei from bone marrow cells using seven MM-specific probes for recurrent aberrations was performed in a total of 215 newly diagnosed patients. RESULTS: Chromosomal abnormalities were detected in 161 (74.9%) MM patients in this study. The most frequent aberration was trisomy(ies) involving only gain of chromosomes in 48 (22.3%) cases. A translocation involving the IGH gene alone or accompanied by trisomy(ies) or by monosomy 13/13q deletion or by both was registered in 80 (37.2%) patients. Atypical patterns such as a deletion of the IGH variable segment (IGHv) on the derivative chromosome 14 or on the native (normal) chromosome 14, biallelic deletion of IGHv, deletion of the IGH constant segment on the rearranged chromosome14 and extra fusions were noticed in 21 (9.8%) patients with an IGH rearrangement. Monosomy 13/deletion 13q was identified singly or as part of a complex karyotype in 74 patients (34.4%). Clonal heterogeneity and additional abnormalities including TP53 deletion and monosomies of chromosomes 4, 9, 14 and 16 were recorded in 18.6% and 16.3% of patients respectively. Patients with abnormalities exhibited plasmacytosis, reduced hemoglobin value and high level of ß2-microglobulin. CONCLUSIONS: A lower median age and a low frequency of IGH translocations particularly t(11;14) and chromosome 13 abnormalities suggest ethnic diversity. Further investigations on genetic alterations including IGH deletions will contribute to improved insights into the biology of myeloma disease, risk stratification and patient management.
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spelling pubmed-64855532019-05-13 Cytogenetic Abnormalities in Multiple Myeloma Patients at a Tertiary Healthcare Center in India Govindasamy, Perumal Pandurangan, Prabu Tarigopula, Anil Mani, Rama Samuel, Chandra R Asian Pac J Cancer Prev Research Article OBJECTIVE: Multiple myeloma (MM) is a clinically and genetically heterogeneous plasma cell neoplasm. The prognosis of MM patients is dependent on several factors including the patient’s age, the stage of disease and genetic alterations. This study aimed to determine the frequency of common chromosomal abnormalities and their significance in MM patients referred to a tertiary healthcare center in India. METHODS: Fluorescence in situ hybridization on interphase nuclei from bone marrow cells using seven MM-specific probes for recurrent aberrations was performed in a total of 215 newly diagnosed patients. RESULTS: Chromosomal abnormalities were detected in 161 (74.9%) MM patients in this study. The most frequent aberration was trisomy(ies) involving only gain of chromosomes in 48 (22.3%) cases. A translocation involving the IGH gene alone or accompanied by trisomy(ies) or by monosomy 13/13q deletion or by both was registered in 80 (37.2%) patients. Atypical patterns such as a deletion of the IGH variable segment (IGHv) on the derivative chromosome 14 or on the native (normal) chromosome 14, biallelic deletion of IGHv, deletion of the IGH constant segment on the rearranged chromosome14 and extra fusions were noticed in 21 (9.8%) patients with an IGH rearrangement. Monosomy 13/deletion 13q was identified singly or as part of a complex karyotype in 74 patients (34.4%). Clonal heterogeneity and additional abnormalities including TP53 deletion and monosomies of chromosomes 4, 9, 14 and 16 were recorded in 18.6% and 16.3% of patients respectively. Patients with abnormalities exhibited plasmacytosis, reduced hemoglobin value and high level of ß2-microglobulin. CONCLUSIONS: A lower median age and a low frequency of IGH translocations particularly t(11;14) and chromosome 13 abnormalities suggest ethnic diversity. Further investigations on genetic alterations including IGH deletions will contribute to improved insights into the biology of myeloma disease, risk stratification and patient management. West Asia Organization for Cancer Prevention 2019 /pmc/articles/PMC6485553/ /pubmed/30678438 http://dx.doi.org/10.31557/APJCP.2019.20.1.235 Text en Copyright: © Asian Pacific Journal of Cancer Prevention http://creativecommons.org/licenses/BY-SA/4.0 This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License
spellingShingle Research Article
Govindasamy, Perumal
Pandurangan, Prabu
Tarigopula, Anil
Mani, Rama
Samuel, Chandra R
Cytogenetic Abnormalities in Multiple Myeloma Patients at a Tertiary Healthcare Center in India
title Cytogenetic Abnormalities in Multiple Myeloma Patients at a Tertiary Healthcare Center in India
title_full Cytogenetic Abnormalities in Multiple Myeloma Patients at a Tertiary Healthcare Center in India
title_fullStr Cytogenetic Abnormalities in Multiple Myeloma Patients at a Tertiary Healthcare Center in India
title_full_unstemmed Cytogenetic Abnormalities in Multiple Myeloma Patients at a Tertiary Healthcare Center in India
title_short Cytogenetic Abnormalities in Multiple Myeloma Patients at a Tertiary Healthcare Center in India
title_sort cytogenetic abnormalities in multiple myeloma patients at a tertiary healthcare center in india
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6485553/
https://www.ncbi.nlm.nih.gov/pubmed/30678438
http://dx.doi.org/10.31557/APJCP.2019.20.1.235
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