Changes in Management After 18F-DCFPyL PSMA PET in Patients Undergoing Postprostatectomy Radiotherapy, with Early Biochemical Response Outcomes

被引:8
作者
Ng, Michael [1 ]
Guerrieri, Mario [2 ]
Wong, Lih Ming [3 ,4 ]
Taubman, Kim [5 ]
Sutherland, Tom [6 ,7 ]
Benson, Angela [8 ]
Byrne, Graeme [9 ]
Koschel, Sam [8 ]
Yap, Kelvin [6 ]
Starmans, Michelle [8 ]
Ong, Grace [10 ]
Macleod, Craig [11 ]
Foo, Marcus [12 ]
Chao, Michael [13 ]
机构
[1] St Vincents Hosp, GenesisCare, Melbourne, Vic, Australia
[2] GenesisCare, Footscray, Vic, Australia
[3] Univ Melbourne, Dept Surg, Melbourne, Vic, Australia
[4] St Vincents Hosp, Dept Surg, Melbourne, Vic, Australia
[5] St Vincents Hosp, Dept Nucl Med, Melbourne, Vic, Australia
[6] St Vincents Hosp, Dept Med Imaging, Melbourne, Vic, Australia
[7] Univ Melbourne, Fac Med, Melbourne, Vic, Australia
[8] GenesisCare Canc Care Res, Melbourne, Vic, Australia
[9] La Trobe Univ, Stat Consultancy Platform, Melbourne, Vic, Australia
[10] GenesisCare, Shepparton, Vic, Australia
[11] GenesisCare, Albury, NSW, Australia
[12] GenesisCare, Berwick, Vic, Australia
[13] GenesisCare, Ringwood, Vic, Australia
关键词
18F-DCFPyL; management change; prostate cancer; prostatectomy; PET; PSMA; PROSTATE-CANCER RECURRENCE; RADICAL PROSTATECTOMY; SALVAGE RADIOTHERAPY; RADIATION-THERAPY; ADJUVANT RADIOTHERAPY; CONSENSUS GUIDELINES; MEMBRANE ANTIGEN; LYMPH-NODE; GA-68-PSMA; IMPACT;
D O I
10.2967/jnumed.121.263521
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
Prostate-specific membrane antigen (PSMA) tracers have increased sensitivity in the detection of prostate cancer, compared with conventional imaging. We assessed the management impact of F-18-DCFPyL PSMA PET/CT in patients with prostate-specific antigen (PSA) recurrence after radical prostatectomy (RP) and report early biochemical response in patients who underwent radiation treatment. Methods: One hundred patients were enrolled into a prospective study, with a prior RP for prostate cancer, a PSA of 0.2-2.0 ng/mL, and no prior treatment. All patients underwent diagnostic CT and PSMA PET/CT, and management intent was completed at 3 time points (original, post-CT, and post-PSMA) and compared. Patients who underwent radiotherapy with 6-mo PSA response data are presented. Results: Ninety-eight patients are reported, with a median PSA of 0.32 ng/mL (95% CI, 0.28-0.36), pT3a/b disease in 71.4%, and an International Society of Urological Pathology grade group of at least 3 in 59.2%. PSMA PET/CT detected disease in 46.9% of patients, compared with 15.5% using diagnostic CT (PSMA PET, 29.2% local recurrence and 29.6% pelvic nodal disease). A major change in management intent was higher after PSMA than after CT (12.5% vs. 3.2%, P = 0.010), as was a moderate change in intent (31.3% vs. 13.7%, P = 0.001). The most common change was an increase in the recommendation for elective pelvic radiation (from 15.6% to 33.3%), nodal boost (from 0% to 22.9%), and use of concurrent androgen deprivation therapy (ADT) (from 22.9% to 41.7%) from original to post-PSMA intent because of detection of nodal disease. Eighty-six patients underwent F-18-DCFPyL-guided radiotherapy. Fifty-five of 86 patients either did not receive ADT or recovered after ADT, with an 18-mo PSA response from 0.32 to 0.02 ng/mL; 94.5% of patients had a PSA of no more than 0.20 ng/mL, and 74.5% had a PSA of no more than 0.03 ng/mL. Conclusion: F-18-DCFPyL PET/CT has a significant impact on management intent in patients being considered for salvage radiotherapy after RP with PSA recurrence. Increased detection of disease, particularly in the pelvic lymph nodes, resulted in increased pelvic irradiation and concurrent ADT use. Early results in patients who are staged with F-18-DCFPyL PET/CT show a favorable PSA response.
引用
收藏
页码:1343 / 1348
页数:6
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