Lung uptake of fluorine-18 fluoroethyl-choline PET-CT in patients with prostate cancer

被引:0
|
作者
Pizzuto, Daniele A. [1 ]
Annunziata, Salvatore [1 ]
Ieria, Francesco P. [1 ]
Caldarella, Carmelo [2 ]
Isgro, Maria A. [3 ]
Lanni, Valerio [2 ]
Bencivenga, Gaia [4 ]
Rufini, Vittoria [1 ]
Giordano, Alessandro [1 ]
机构
[1] Univ Cattolica Sacro Cuore, Fdn Policlin Univ A Gemelli, Unita Operat Complessa Med Nucl, Ist Med Nucl,IRCCS, Rome, Italy
[2] Fdn Policlin Univ A Gemelli, Unit Nucl Med, Unita Operat Complessa Med Nucl, Rome, Italy
[3] Circolo & Fdn Macchi Hosp, Chem Clin & Hematol Anal Lab, Varese, Italy
[4] Fdn Policlin Univ A Gemelli, PET CT Ctr, Unita Operat Complessa Med Nucl, Rome, Italy
关键词
Prostate; Lung; Neoplasm metastasis; Choline; PSA DOUBLING TIME; RADICAL PROSTATECTOMY; F-18-CHOLINE PET/CT; BIOCHEMICAL RECURRENCE; DISEASE RECURRENCE; TRIGGER PSA; RELAPSE; ANTIGEN; METASTASES; EXPERIENCE;
D O I
10.23736/S1824-4785.18.02985-0
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
BACKGROUND: Metastatic spreading to the lungs is a negative prognostic factor in patients with prostate cancer (PC). Aim of our study was to assess the prevalence of lung PC metastases in patients with fluorine-18 fluoroethyl-choline (F-18-FECh) PET-CT positive lung lesions and the role of Gleason Score (GS) and common biochemical markers in predicting metastatic spreading to the lungs. METHODS: We retrospectively evaluated the scans of 1283 patients ongoing (F-18-FECh) PET-CT for PC between May 2010 and July 2014. Patients with lung lesion with F-18-FECh uptake were included. Data concerning GS at diagnosis, "trigger" prostate-specific antigen (PSAtr), PSA doubling time (PSAdt), PSA velocity (PSAvel) and ongoing androgen deprivation therapy were collected. PET-CT findings were confirmed by histology or follow-up (FU) and classified as follows: inflammation, primary lung cancer or metastases from tumor other than PC, and lung metastases from PC. RESULTS: Twenty-two patients with F-18-FECh positive lung lesion and available histology or FU were identified. PSAdt was significantly (P=0.029) shorter in patients with lung metastases from PC (median PSAdt 1.7 months, interquartile range [IQR] 1.5-4.1 months) than in patients without lung PC relapse (median PSAdt 6.7 months, IQR 3.9-7.8); PSAvel was significantly (P=0.019) higher in patients with lung metastases from PC (median PSAveI 3.2 ng/mUmonth, IQR 0.65-6.65 nginiLlmonth) than in patients without lung PC relapse (median PSAveI 0.3 ng/mL/ month, IQR 0.2-0.5 ng/milmonth). Patients with lung metastases from PC had significantly (P=0.006) higher GS at diagnosis (median GS 8) than the other ones (median GS 7). CONCLUSIONS: Our analysis shows that the prevalence of F-18-FECh positive lung metastases in patients with PC, especially with higher GS at diagnosis, is higher in presence of a steady increase in PSA values, confirmed by higher PSAveI and shorter PSAdt.
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收藏
页码:387 / 393
页数:7
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