Gkioka Annita-Ioanna, Gkiokas Alexandros, Papadatou-Gigante Mavra, Alexandropoulos Alexandros, Tryfou Thomai-Marina, Koudouna Aspasia, Bartzi Vasiliki, Kyrtsonis Marie-Christine
Hematology Section of First Department of Propedeutic Internal Medicine, National and Kapodistrian University of Athens, 11527 Athens, Greece.
Int J Mol Sci. 2025 Jun 30;26(13):6341. doi: 10.3390/ijms26136341.
Serum cereblon (CRBN) has been proposed as a target protein for immunomodulatory drugs (IMiDs). IMiDs are one of the backbone treatment options in multiple myeloma (MM), rendering CRBN an intriguing candidate for use as a biomarker in clinical settings. Ninety-two (92) MM patients, mostly relapsed/refractory and a few at diagnosis, were included in the study, from lenalidomide-dexamethasone (LD) initiation until last follow-up or death. Median CRBN at LD initiation ( = 68) treatment was 247 pg/mL (range, 0-9760 pg/mL), at the time of best response (BR) status ( = 59) 142.5 pg/mL (range, 0-9940 pg/mL) and in patients with relapse/refractory MM to LD regimen (N = 54) 298 pg/mL (range, 0-9840 pg/mL). CRBN in healthy individuals was almost undetectable and significantly lower compared to the CRBN at LD initiation ( = 0.003), at BR to LD ( = 0.012) and at relapse to LD ( = 0.002). CRBN was significantly lower at BR in contrast to LD initiation and relapse to LD ( = 0.04, = 0.028). High levels of CRBN at treatment initiation correlated with early relapse to LD (≤12 months) ( = 0.03). Seven-year survival was improved in patients with CRBN levels below median measured at the time of LD initiation ( = 0.013) as well as at BR ( = 0.032). CRBN was associated with treatment response and is predictive of survival after LD.
血清脑啡肽(CRBN)已被提议作为免疫调节药物(IMiDs)的靶蛋白。IMiDs是多发性骨髓瘤(MM)的主要治疗选择之一,这使得CRBN成为临床上用作生物标志物的一个有趣候选物。该研究纳入了92例MM患者,大多数为复发/难治性患者,少数为初诊患者,从开始使用来那度胺-地塞米松(LD)治疗直至最后随访或死亡。LD起始治疗时(n = 68)CRBN的中位数为247 pg/mL(范围为0 - 9760 pg/mL),在最佳缓解(BR)状态时(n = 59)为142.5 pg/mL(范围为0 - 9940 pg/mL),在对LD方案复发/难治的MM患者中(N = 54)为298 pg/mL(范围为0 - 9840 pg/mL)。健康个体中的CRBN几乎检测不到,与LD起始治疗时(P = 0.003)、对LD达到BR时(P = 0.012)以及对LD复发时(P = 0.002)的CRBN相比显著更低。与LD起始治疗和对LD复发相比,BR时的CRBN显著更低(P = 0.04,P = 0.028)。治疗开始时CRBN水平高与LD早期复发(≤12个月)相关(P = 0.03)。LD起始治疗时以及BR时CRBN水平低于中位数的患者7年生存率得到改善(P = 0.013以及P = 0.032)。CRBN与治疗反应相关,并且可预测LD治疗后的生存情况。