[68Ga]Pentixafor PET/CT for staging and prognostic assessment of newly diagnosed multiple myeloma: comparison to [18F]FDG PET/CT

被引:3
作者
Chen, Zhenying [1 ,2 ]
Yang, Apeng [3 ]
Chen, Aihong [1 ,2 ]
Dong, Jinfeng [3 ]
Lin, Junfang [3 ]
Huang, Chao [1 ,2 ]
Zhang, Jiaying [1 ,2 ]
Liu, Huimin [1 ,2 ]
Zeng, Zhiyong [3 ]
Miao, Weibing [1 ,2 ,4 ]
机构
[1] Fujian Med Univ, Affiliated Hosp 1, Dept Nucl Med, Fuzhou 350005, Peoples R China
[2] Fujian Med Univ, Affiliated Hosp 1, Natl Reg Med Ctr, Dept Nucl Med, Binhai Campus, Fuzhou 350212, Peoples R China
[3] Fujian Med Univ, Affiliated Hosp 1, Dept Hematol, Fuzhou 350005, Peoples R China
[4] Fujian Med Univ, Affiliated Hosp 1, Fujian Key Lab Precis Med Canc, Fuzhou 350005, Peoples R China
关键词
Multiple myeloma; Ga-68]Pentixafor; F-18]FDG; PET/CT; Durie-Salmon PLUS staging system; Prognosis; F-18-FDG PET/CT; DURIE-SALMON; BONE-MARROW; DISEASE; SYSTEM; INFILTRATION; TOMOGRAPHY; EXPRESSION; CXCR4; MRI;
D O I
10.1007/s00259-024-06621-0
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Purpose To evaluate the prognostic performance of [Ga-68]Pentixafor PET/CT at baseline for staging of patients with newly diagnosed multiple myeloma (MM) and to compare it with [F-18]FDG PET/CT and the Revised-International Staging System (R-ISS). Methods Patients who underwent [Ga-68]Pentixafor and [F-18]FDG PET/CT imaging were retrospectively included. Patient staging was performed according to the Durie-Salmon PLUS staging system based on [Ga-68]Pentixafor PET/CT and [F-18]FDG PET/CT images, and the R-ISS. Progression-free survival (PFS) at patient follow-up was estimated using the Kaplan-Meier estimator and compared using the log-rank test. Area under the receiver operating characteristic curve (AUC) was calculated to assess predictive performance. Results Fifty-five MM patients were evaluated. Compared with [F-18]FDG PET, [Ga-68]Pentixafor PET detected 25 patients as the same stage, while 26 patients were upstaged and 4 patients were downstaged (P = 0.001). After considering the low-dose CT data, there was no statistically significant difference in the number of patients classified in each stage using [Ga-68]Pentixafor PET/CT and [F-18]FDG PET/CT (P = 0.091). [Ga-68]Pentixafor PET/CT-based staging discriminated PFS outcomes in patients with different disease stages (stage I vs. stage II, stage I vs. stage III, and stage II vs. stage III; all P < 0.05), whereas for [F-18]FDG PET/CT, there was only a difference in median PFS between stage I and III (P = 0.021). When staged by R-ISS, the median PFS for stage III was significantly lower than that for stage I and II (P = 0.008 and 0.035, respectively). When predicting 2-year PFS based on staging, the AUC of [Ga-68]Pentixafor PET/CT was significantly higher than that of [Ga-68]Pentixafor PET (0.923 vs. 0.821, P = 0.002), [F-18]FDG PET (0.923 vs. 0.752 P = 0.002), and R-ISS (0.923 vs. 0.776, P = 0.005). Conclusions [Ga-68]Pentixafor PET/CT-based staging possesses substantial potential to predict disease progression in newly diagnosed MM patients.
引用
收藏
页码:1926 / 1936
页数:11
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