Morawitz Janna, Kirchner Julian, Hertelendy Johannes, Loberg Christina, Schimmöller Lars, Dabir Mardjan, Häberle Lena, Mamlins Eduards, Antke Christina, Arsov Christian, Antoch Gerald, Sawicki Lino M
Department of Diagnostic and Interventional Radiology, Medical Faculty, University Dusseldorf, Moorenstrasse 5, 40225, Düsseldorf, Germany.
Department of Nuclear Medicine, Medical Faculty, University Dusseldorf, 40225, Düsseldorf, Germany.
EJNMMI Res. 2022 Mar 4;12(1):12. doi: 10.1186/s13550-022-00885-z.
To assess the diagnostic value of an additional late-phase PET/CT scan after urination as part of Ga-PSMA-11 PET/CT for the restaging of patients with biochemically recurrent prostate cancer (BCR).
This retrospective trial included patients with BCR following radical prostatectomy, who underwent standard whole-body early-phase PET/CT performed 105 ± 45 min and an additional late-phase PET/CT performed 159 ± 13 min after injection of Ga-PSMA-11. Late-phase PET/CT covered a body volume from below the liver to the upper thighs and was conducted after patients had used the bathroom to empty their urinary bladder. Early- and late-phase images were evaluated regarding lesion count, type, localisation, and SUVmax. Reference standard was histopathology and/or follow-up imaging.
Whole-body early-phase PET/CT detected 93 prostate cancer lesions in 33 patients. Late-phase PET/CT detected two additional lesions in two patients, both local recurrences. In total, there were 57 nodal, 28 bone, and 3 lung metastases, and 7 local recurrences. Between early- and late-phase PET/CT, lymph node metastases showed a significant increase of SUVmax from 14.5 ± 11.6 to 21.5 ± 17.6 (p = 0.00007), translating to a factor of + 1.6. Benign lymph nodes in the respective regions showed a significantly lower increase of SUVmax of 1.4 ± 0.5 to 1.7 ± 0.5 (p = 0.0014, factor of + 1.2). Local recurrences and bone metastases had a SUVmax on late-phase PET/CT that was + 1.7 and + 1.1 times higher than the SUVmax on early-phase PET/CT, respectively.
In patients with BCR following radical prostatectomy, an additional abdomino-pelvic late-phase Ga-PSMA-11 PET/CT scan performed after emptying the urinary bladder may help to detect local recurrences missed on standard whole-body Ga-PSMA-11 PET/CT. Lymph node metastases show a higher SUVmax and a stronger increase of SUVmax than benign lymph nodes on late-phase PET/CT, hence, biphasic Ga-PSMA-11 PET/CT might help to distinguish between malignant and benign nodes. Bone metastases, and especially local recurrences, also demonstrate a metabolic increase over time.
评估排尿后额外进行的晚期PET/CT扫描作为镓-PSMA-11 PET/CT的一部分对生化复发前列腺癌(BCR)患者进行再分期的诊断价值。
这项回顾性试验纳入了根治性前列腺切除术后发生BCR的患者,这些患者在注射镓-PSMA-11后105±45分钟接受了标准的全身早期PET/CT检查,并在159±13分钟后额外进行了晚期PET/CT检查。晚期PET/CT覆盖从肝脏下方到大腿上部的身体区域,在患者排空膀胱后进行。对早期和晚期图像的病灶数量、类型、定位和SUVmax进行评估。参考标准为组织病理学和/或随访成像。
全身早期PET/CT在33例患者中检测到93个前列腺癌病灶。晚期PET/CT在2例患者中又检测到2个病灶,均为局部复发。总共有57个淋巴结转移、28个骨转移和3个肺转移,以及7个局部复发。在早期和晚期PET/CT之间,淋巴结转移的SUVmax从14.5±11.6显著增加到21.5±17.6(p = 0.00007),增幅为+1.6倍。相应区域的良性淋巴结SUVmax的增幅显著较低,从1.4±0.5增加到1.7±0.5(p = 0.0014,增幅为+1.2倍)。晚期PET/CT上局部复发和骨转移的SUVmax分别比早期PET/CT上的SUVmax高+1.7倍和+1.1倍。
对于根治性前列腺切除术后发生BCR的患者,排空膀胱后额外进行的腹部-盆腔晚期镓-PSMA-11 PET/CT扫描可能有助于检测标准全身镓-PSMA-11 PET/CT遗漏的局部复发。在晚期PET/CT上,淋巴结转移的SUVmax更高,且比良性淋巴结的SUVmax增加更明显,因此,双期镓-PSMA-11 PET/CT可能有助于区分恶性和良性淋巴结。骨转移,尤其是局部复发,也显示出随时间的代谢增加。