Pan Qingqing, Chen Zhenying, Liu Silu, Zhang Hongzhe, Feng Jie, Miao Weibing, Li Fang, Cao Xinxin, Luo Yaping
Department of Nuclear Medicine, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
State Key Laboratory of Common Mechanism Research for Major Diseases, Wangfujing, Dongcheng District, Beijing, 100730, P. R. China.
EJNMMI Res. 2025 Jun 20;15(1):74. doi: 10.1186/s13550-025-01262-2.
We aim to investigate the prognostic value of [Ga]Ga-Pentixafor PET/CT in multiple myeloma (MM) patients.
This is a retrospective analysis of a prospective cohort study. Twenty-five patients with treatment-naïve, newly diagnosed MM were included. All participants underwent [Ga]Ga-Pentixafor PET/CT scans at baseline and after first-line chemotherapy. The endpoints included the time to progression (TTP) and the time to next treatment (TTNT). The correlation between PET/CT characteristics and survival was then analyzed. Patients with a decline in SUVmax of bone marrow of less than 40% from baseline demonstrated significantly shorter TTP and TTNT (estimated median TTP, 27.5 months [95% CI, 16.7-38.2] vs. not reached, P = 0.047; estimated median TTNT, 31.8 months [95% CI, 20.8-42.8] vs. not reached, P = 0.012). Patients with visually reduced splenic uptake in the follow-up [Ga]Ga-Pentixafor PET/CT from baseline exhibited significantly shorter TTP and TTNT (estimated median TTP, 24.4 months [95% CI, 7.9-24.4] vs. not reached, P = 0.018; estimated median TTNT, 31.9 months [95% CI, 18.5-31.9] vs. not reached, P = 0.043). A 20% reduction in splenic SUVmax was identified as a predictive indicator for shorter TTP and TTNT (estimated median TTP, 24.4 months [95% CI, 14.5-24.4] vs. not reached, P = 0.025; estimated mean TTNT, 31.9 months [95% CI, 18.5-31.9] vs. not reached, P = 0.048). Patients with splenic SUVmax < 5.0 at follow-up also exhibited significantly shorter TTP and TTNT. However, the splenic SUVmax at baseline PET/CT was not predictive of TTP or TTNT (P > 0.05).
Reduced splenic uptake of [Ga]Ga-Pentixafor following first-line chemotherapy was predictive for poor prognosis in patients with newly diagnosed MM, while baseline splenic uptake is not associated with prognosis.
ClinicalTrials. NCT03436342 Registered 25 October 2017, https://register.
gov/prs/app/action/SelectProtocol?sid=S0007IL2&selectaction=Edit&uid=U0001JRW&ts=6&cx=-3sdpwu .
NCT04504526 Registered 6 August 2020, https://clinicaltrials.gov/study/NCT04504526?cond=NCT04504526&rank=1 .
我们旨在研究[镓]镓-喷替酸五钠正电子发射断层扫描/计算机断层扫描([Ga]Ga-Pentixafor PET/CT)在多发性骨髓瘤(MM)患者中的预后价值。
这是一项对前瞻性队列研究的回顾性分析。纳入了25例未经治疗的新诊断MM患者。所有参与者在基线和一线化疗后均接受了[Ga]Ga-Pentixafor PET/CT扫描。终点包括疾病进展时间(TTP)和下次治疗时间(TTNT)。然后分析了PET/CT特征与生存之间的相关性。骨髓SUVmax较基线下降小于40%的患者显示TTP和TTNT显著缩短(估计中位TTP,27.5个月[95%CI,16.7 - 38.2] vs.未达到,P = 0.047;估计中位TTNT,31.8个月[95%CI,20.8 - 42.8] vs.未达到,P = 0.012)。随访时[Ga]Ga-Pentixafor PET/CT显示脾脏摄取较基线视觉上降低的患者,TTP和TTNT显著缩短(估计中位TTP,24.4个月[95%CI,7.9 - 24.4] vs.未达到,P = 0.018;估计中位TTNT,31.9个月[95%CI,18.5 - 31.9] vs.未达到,P = 0.043)。脾脏SUVmax降低20%被确定为TTP和TTNT缩短的预测指标(估计中位TTP,24.4个月[95%CI,14.5 - 24.4] vs.未达到,P = 0.025;估计平均TTNT,31.9个月[95%CI,18.5 - 31.9] vs.未达到,P = 0.0