68Ga-PSMA has a high detection rate of prostate cancer recurrence outside the prostatic fossa in patients being considered for salvage radiation treatment

被引:237
作者
van Leeuwen, Pim J. [1 ,2 ]
Stricker, Phillip [1 ,2 ]
Hruby, George [3 ,4 ,5 ]
Kneebone, Andrew [3 ,4 ,5 ]
Ting, Francis [1 ,2 ]
Thompson, Ben [2 ]
Quoc Nguyen [2 ]
Ho, Bao [6 ]
Emmett, Louise [6 ,7 ]
机构
[1] St Vincents Clin, St Vincents Prostate Canc Ctr, Sydney, NSW, Australia
[2] Kinghorn Canc Ctr, Garvan Inst Med Res, Australian Prostate Canc Res Ctr New South Wales, Sydney, NSW, Australia
[3] Royal N Shore Hosp, Northern Sydney Canc Ctr, Dept Radiat Oncol, St Leonards, NSW 2065, Australia
[4] Univ Sydney, Sydney, NSW 2006, Australia
[5] Univ Sydney, Northern Clin Sch, St Leonards, NSW, Australia
[6] St Vincents Publ Hosp, Dept Diagnost Imaging, Sydney, NSW, Australia
[7] Univ New S Wales, Sydney, NSW, Australia
关键词
Ga-68-PSMA; PET/CT; prostate cancer; radical prostatectomy; biochemical progression; salvage radiation treatment; RADIOTHERAPY; GUIDELINES; PET/CT; LIGAND;
D O I
10.1111/bju.13397
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Objectives To examine the detection rates of Ga-68-PSMA-positron emission tomography (PET)/computed tomography (CT) in patients with biochemical recurrence (BCR) after radical prostatectomy (RP), and also the impact on their management. Materials and Methods A total of 300 consecutive patients with prostate cancer (PCa) who underwent Ga-68-PSMA-PET/CT between February and July 2015 were prospectively included in the Prostate Cancer Imaging (ProCan-I) database. For the present analysis, we included patients with BCR (prostate-specific antigen [PSA] level >= 0.05 and <1.0 ng/mL) after RP, who were being considered for salvage radiation therapy (RT) according to the Faculty of Radiation Oncology Genito-Urinary Group (FROGG) guidelines. Two readers assessed each Ga-68-PSMA-PET/CT, and all positive lesions were assigned to an anatomical location. For each patient, the clinical and pathological features were recorded, their association with pathological Ga-68-PSMA uptake was investigated, and detection rates were determined according to PSA level. Results A total of 70 patients were included, and 53 positive Ga-68-PSMA lesions were detected in 38 (54%) patients. Among patients with PSA levels 0.05-0.09 ng/mL, 8% were definitely positive; the corresponding percentages for the other PSA ranges were as follows: PSA 0.1-0.19 ng/mL, 23%; PSA 0.2-0.29 ng/mL, 58%; PSA 0.3-0.49 ng/mL, 36%; and PSA 0.5-0.99 ng/mL, 57%. Eighteen of 70 patients (27%) had pathological Ga-68-PSMA uptake in the prostatic fossa, 11 (14.3%) in the pelvic nodes, and five (4.3%) in both the fossa and pelvic lymph nodes. Finally, there was uptake outside the pelvis with or without a lesion in the fossa or pelvic lymph nodes in four cases (8.6%). As a result of the Ga-68-PSMA findings there was a major management change in 20 (28.6%) patients. Conclusions Ga-68-PSMA appears to be useful for re-staging of PCa in patients with rising PSA levels who are being considered for salvage RT even at PSA levels <0.5 ng/mL. These results underline the need for further prospective trials to evaluate the changes in RT volume or management attributable to Ga-68-PSMA findings.
引用
收藏
页码:732 / 739
页数:8
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