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F-DCFPyL PET/CT 用于初诊和生化复发前列腺癌:前瞻性伴有病理证实的试验。

F-DCFPyL PET/CT for Initially Diagnosed and Biochemically Recurrent Prostate Cancer: Prospective Trial with Pathologic Confirmation.

机构信息

From the Departments of Molecular Imaging and Therapy (G.A.U., B.T.), Urology (J.B., R.T., J.Y.), Radiation Oncology (C.C., K.L.), and Radiology (T.P., T.T.), Hoag Family Cancer Institute, 16105 Sand Canyon Ave, Irvine, CA 92618; Departments of Radiology and Translational Genomics, University of Southern California, Los Angeles, Calif (G.A.U.); Department of Epidemiology and Biostatistics, Memorial Sloan-Kettering Cancer Center, New York, NY (A.M.); The Russell H. Morgan Department of Radiology and Radiological Science, Johns Hopkins University School of Medicine, Baltimore, Md (S.P.R.); and Molecular Imaging Branch, National Cancer Institute, National Institutes of Health, Bethesda, Md (L.L., E.M., P.C.).

出版信息

Radiology. 2022 Nov;305(2):419-428. doi: 10.1148/radiol.220218. Epub 2022 Jul 19.

Abstract

Background Prostate-specific membrane antigen (PSMA) PET is standard for newly diagnosed high-risk and biochemically recurrent (BCR) prostate cancer. Although studies suggest high specificity of 2-(3-{1-carboxy-5-[(6-[(18)F]fluoro-pyridine-3-carbonyl)-amino]-pentyl}-ureido)-pentanedioic acid (DCFPyL) for targeting PSMA, false-positive findings have been identified and most studies lack histologic confirmation of malignancy. Purpose To estimate the positive predictive value (PPV) of DCFPyL PET/CT by providing histopathologic proof for DCFPyL-avid lesions suspected of being distant metastases at initial diagnosis and recurrence in BCR prostate cancer. Materials and Methods In this prospective trial, men with newly diagnosed high-risk prostate cancer (sample 1) or BCR prostate cancer and negative findings at conventional CT and/or bone scanning (sample 2) were enrolled between January and December 2021. All men underwent DCFPyL PET/CT. Suspected distant metastases and/or recurrences were biopsied. PPV was calculated. Results A total of 92 men with newly diagnosed prostate cancer (median age, 70 years; IQR, 64-75 years) (sample 1) and 92 men with BCR prostate cancer (median age, 71 years; IQR, 66-75 years) (sample 2) were enrolled. In sample 1, 25 of the 92 men (27%) demonstrated DCFPyL-avid lesions suspicious for distant metastases. Biopsy was performed in 23 of the 25 men (92%), with 17 of the 23 (74%) biopsies positive for malignancy and six (26%) benign. Of the six benign biopsies, three were solitary rib foci and three were solitary pelvic bone foci. In sample 2, 57 of the 92 men (62%) demonstrated DCFPyL-avid lesions suspicious for recurrence. Biopsy was performed in 37 of the 57 men (65%), with 33 of the 37 (89%) biopsies positive for malignancy and four (11%) benign. Of the four benign biopsies, two were subcentimeter pelvic nodes and/or nodules, one was a rib, and one was a pelvic bone focus. Conclusion PET/CT with 2-(3-{1-carboxy-5-[(6-[(18)F]fluoro-pyridine-3-carbonyl)-amino]-pentyl}-ureido)-pentanedioic acid (DCFPyL) had a high biopsy-proven positive predictive value for distant metastases in newly diagnosed prostate cancer (74%) and for recurrence sites in men with biochemical recurrence (89%). However, there were DCFPyL-avid false-positive findings (particularly in ribs and pelvic bones). Solitary DCFPyL avidity in these locations should not be presumed as malignant. Biopsy may still be needed prior to therapy decisions. ClinicalTrials.gov registration no. NCT04700332 © RSNA, 2022 See also the editorial by Zukotynski and Kuo in this issue.

摘要

背景 前列腺特异性膜抗原(PSMA)PET 是新诊断的高危和生化复发(BCR)前列腺癌的标准检查。尽管研究表明,2-(3-{1-羧基-5-[(6-[(18)F]氟吡啶-3-羰基)-氨基]-戊基}-脲基)-戊二酸(DCFPyL)对 PSMA 具有高特异性,但已发现假阳性结果,并且大多数研究缺乏对恶性肿瘤的组织学确认。目的 通过对新诊断的高危前列腺癌(样本 1)或 BCR 前列腺癌且传统 CT 和/或骨扫描阴性(样本 2)患者的 DCFPyL 阳性病变进行组织病理学证实,估计 DCFPyL PET/CT 的阳性预测值(PPV)。这些病变最初被怀疑为远处转移,或在 BCR 前列腺癌中复发。材料与方法 本前瞻性试验纳入了 2021 年 1 月至 12 月间新诊断为高危前列腺癌(中位年龄 70 岁;IQR,64-75 岁)(样本 1)或 BCR 前列腺癌且传统 CT 和/或骨扫描阴性(样本 2)的男性。所有患者均接受了 DCFPyL PET/CT 检查。疑似远处转移和/或复发部位进行了活检。计算了 PPV。结果 共有 92 例新诊断为前列腺癌的男性(中位年龄 70 岁;IQR,64-75 岁)(样本 1)和 92 例 BCR 前列腺癌男性(中位年龄 71 岁;IQR,66-75 岁)(样本 2)纳入研究。在样本 1 中,92 例患者中有 25 例(27%)表现出可疑为远处转移的 DCFPyL 阳性病变。对 23 例患者进行了活检(92%),其中 17 例(74%)活检为恶性,6 例(26%)为良性。在 6 例良性活检中,有 3 例为孤立性肋骨病灶,3 例为孤立性骨盆病灶。在样本 2 中,92 例患者中有 57 例(62%)表现出可疑为复发的 DCFPyL 阳性病变。对 37 例患者进行了活检(65%),其中 33 例(89%)活检为恶性,4 例(11%)为良性。在 4 例良性活检中,2 例为亚厘米级的盆腔淋巴结和/或结节,1 例为肋骨,1 例为骨盆骨病灶。结论 对于新诊断的前列腺癌(74%)和生化复发患者(89%),使用 2-(3-{1-羧基-5-[(6-[(18)F]氟吡啶-3-羰基)-氨基]-戊基}-脲基)-戊二酸(DCFPyL)的 PET/CT 检查具有较高的活检证实的阳性预测值。然而,也存在 DCFPyL 阳性的假阳性结果(尤其是在肋骨和骨盆骨)。在这些部位出现孤立的 DCFPyL 摄取不应被假定为恶性。在做出治疗决策之前,可能仍需要进行活检。临床试验注册编号:NCT04700332 © RSNA,2022 请参见本期杂志中 Zukotynski 和 Kuo 的评论。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/148e/9619197/066913758b93/radiol.220218.VA.jpg

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