The prognostic value of KRAS, NRAS, and BRAF genes mutations in patients with newly diagnosed multiple myeloma

IF 0.8 Q4 HEMATOLOGY
Leukemia Research Reports Pub Date : 2026-01-01 Epub Date: 2026-10-08 DOI:10.1016/j.lrr.2026.100615
Phuong Thao Pham, Hoang Viet Nguyen, Minh Phuong Vu
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引用次数: 0

Abstract

Background

KRAS, NRAS, and BRAF (RAS/RAF) genes mutations play a role in the pathogenesis of multiple myeloma (MM). We conducted this study to investigate whether RAS/RAF genes mutations have a prognostic value in patients with MM.

Material and methods

117 newly diagnosed MM patients underwent the FISH technique to detect high-risk cytogenetic abnormalities and next-generation sequencing (NGS) to detect KRAS, NRAS, BRAF and TP53 mutations.

Results

In the study patient group, patients with the KRAS mutation had significantly longer OS and PFS compared to those with the TP53 mutation; patients with the BRAF mutation had significantly longer OS compared to those with the TP53 mutation. In the patient without high-risk cytogenetics based on FISH, patients with the KRAS mutation had significantly longer OS and PFS compared to those with the TP53 mutation. Conversely, in the patients with high-risk cytogenetics based on FISH, no difference in survival time has been observed among patient groups harboring different gene mutations.

Conclusions

RAS/RAF gene mutations may have important prognostic implications for MM but should be considered in conjunction with other abnormalities, such as chromosomal abnormalities and TP53 mutations.
KRAS、NRAS和BRAF基因突变在新诊断多发性骨髓瘤患者中的预后价值
kras、NRAS和BRAF (RAS/RAF)基因突变在多发性骨髓瘤(MM)的发病机制中起作用。本研究旨在探讨RAS/RAF基因突变是否对MM患者的预后有影响。材料和方法117例新诊断的MM患者采用FISH技术检测高危细胞遗传学异常,并采用下一代测序(NGS)检测KRAS、NRAS、BRAF和TP53突变。结果KRAS突变患者的OS和PFS均明显长于TP53突变患者;BRAF突变患者的OS明显长于TP53突变患者。在基于FISH的无高危细胞遗传学的患者中,与TP53突变患者相比,KRAS突变患者的OS和PFS明显更长。相反,在基于FISH的高危细胞遗传学患者中,携带不同基因突变的患者组之间的生存时间没有差异。结论sras /RAF基因突变可能对MM的预后有重要影响,但应与其他异常(如染色体异常和TP53突变)结合考虑。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Leukemia Research Reports
Leukemia Research Reports Medicine-Oncology
CiteScore
1.70
自引率
0.00%
发文量
70
审稿时长
23 weeks
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