Temporal genomic dynamics shape clinical trajectory in multiple myeloma Journal Article


Authors: Maura, F.; Kaddoura, M.; Poos, A. M.; Baughn, L. B.; Ziccheddu, B.; Bärtsch, M. A.; Cirrincione, A.; Maclachlan, K.; Chojnacka, M.; Diamond, B.; Papadimitriou, M.; Blaney, P.; John, L.; Reichert, P.; Huhn, S.; Gagler, D.; Zhang, Y. M.; Dogan, A.; Lesokhin, A. M.; Davies, F.; Goldschmidt, H.; Fenk, R.; Weisel, K. C.; Mai, E. K.; Korde, N.; Morgan, G. J.; Rajkumar, S. V.; Kumar, S.; Usmani, S.; Landgren, O.; Raab, M. S.; Weinhold, N.
Article Title: Temporal genomic dynamics shape clinical trajectory in multiple myeloma
Abstract: Multiple myeloma evolution is characterized by the accumulation of genomic drivers over time. To unravel this timeline and its impact on clinical outcomes, we analyzed 421 whole-genome sequences from 382 patients. Using clock-like mutational signatures, we estimated a time lag of two to four decades between the initiation of events and diagnosis. We demonstrate that odd-numbered chromosome trisomies in patients with hyperdiploidy can be acquired simultaneously with other chromosomal gains (for example, 1q gain). We show that hyperdiploidy is acquired after immunoglobulin heavy chain translocation when both events co-occur. Finally, patients with early 1q gain had adverse outcomes similar to those with 1q amplification (>1 extra copy), but fared worse than those with late 1q gain. This finding underscores that the 1q gain prognostic impact depends more on the timing of acquisition than on the number of copies gained. Overall, this study contributes to a better understanding of the life history of myeloma and may have prognostic implications.
Keywords: expression; system; translocations; event; dysregulation; monoclonal gammopathy; mutational signatures
Journal Title: Nature Genetics
ISSN: 1061-4036
Publisher: Nature Publishing Group  
Publication status: Online ahead of print
Date Published: 2025-01-01
Online Publication Date: 2025-01-01
Language: English
ACCESSION: WOS:001554567100001
DOI: 10.1038/s41588-025-02292-1
PROVIDER: wos
Notes: Article; Early Access -- Source: Wos
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