Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12188/17642
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dc.contributor.authorKrstevska balkanov, Svetlanaen_US
dc.contributor.authorTrajkova, Sanjaen_US
dc.contributor.authorPivkova Veljanovska, Aleksandraen_US
dc.contributor.authorSpasovski, Dejanen_US
dc.contributor.authorRidova, Nevenkaen_US
dc.contributor.authorKalcev, Goceen_US
dc.contributor.authorPanovska Stavridis, Irinaen_US
dc.date.accessioned2022-05-17T10:01:34Z-
dc.date.available2022-05-17T10:01:34Z-
dc.date.issued2022-05-
dc.identifier.issn2284-6808-
dc.identifier.urihttp://hdl.handle.net/20.500.12188/17642-
dc.description.abstractAbstract: Multiple Myeloma (MM) is a hematological malignity associated with the proliferation and accumulation of bone marrow terminally differentiated plasma cells. The outcomes of patients with MM have dramatically improved over the past decade with the establishment of novel agents. Nonetheless, the disease presents considerable heterogeneity in clinical course, presentation, and survival. Molecular and chromosomal analyses were performed on 46 patients with MM. The survival time of patients with MM concerning molecular and chromosome stratification showed that 20% of them were with high risk [hypodiploid (gain1q, loss1p) Del17p, Del13q, t(11;14) t(4;14) and multiple mutations] who survived 60 months and the median survival time in these patients was 20.8 months. In patients with MM who had a standard risk, death outcome was not registered during the observation period. Taking into account, all MM patients included in our study, Bence Jones proteins in the urine wеre present in 35.8% of ММ patients, while in 64.2%, their presence was not observed. The percentage difference is statistically significant The utilization of these crucial biomarkers in the clinical background for this disease in the future can only be achieved through thorough evaluation and validation in clinical trials.en_US
dc.language.isoenen_US
dc.relation.ispartofLetters in Applied NanoBioScienceen_US
dc.subjectmultiple myelomaen_US
dc.subjectBence-Jones proteinen_US
dc.subjectchromosomal aberrationsen_US
dc.subjectmolecular analysisen_US
dc.titleChromosomal Aberrations and Bence-Jones Proteins as a Significant Biomarkers in Multiple Myelomaen_US
dc.typeArticleen_US
dc.identifier.doi10.33263/LIANBS123.074-
item.fulltextWith Fulltext-
item.grantfulltextopen-
crisitem.author.deptFaculty of Medicine-
crisitem.author.deptFaculty of Medicine-
crisitem.author.deptFaculty of Medicine-
crisitem.author.deptFaculty of Medicine-
Appears in Collections:Faculty of Medicine: Journal Articles
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Chromosomal abberation, 2022, Volume 12, Issue 3, 2022, 74.pdf216.01 kBAdobe PDFView/Open
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