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1159

Parameter
Biomarker del (17p)、t (4;14)、t (14;16)、1q+) Full name chromosome abnormality( Deletion of the short arm of chromosome 17、Reciprocal translocation between chromosome 4 and chromosome 14、Reciprocal translocation between chromosome 14 and chromosome 16、Gain/Amplification of the long arm of chromosome 1 Molecular Type nucleic acid
Molecular Formula Molecular Weight Core Functional Dimensions prognosis, risk stratification
Disease Multiple Myeloma (MM) Disease Subtypes /
Organ Multiple Myeloma (MM) Test Sample / Technology Platform marrow
Pathobiological Mechanisms del(17p) leads to TP53 deletion, t(4;14) activates FGFR3/MMSET, t(14;16) overexpresses c-MAF, and 1q+ amplification of CKS1B, all of which enhance tumor invasiveness.
Clinical Availability Status Routine clinical use/guideline recommendations
Notes and Dynamics High-risk abnormal patients exhibit poor response to conventional regimens, and intensive therapy (e.g., double ASCT, CAR-T) is recommended; the incidence of 1q+ is elevated in relapsed patients and may serve as a resistance monitoring indicator.

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This study was supported by the Scientific Research Innovation Capability Support Project for Young Faculty (SRICSPYF-ZY2025112), the Fundamental and Interdisciplinary Disciplines Breakthrough Plan of the Ministry of Education of China (JYB2025XDXM612)

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