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Detection level and pattern of positive lesions using PSMA PET/CT for staging prior to radiation therapy
Radiation Oncologyvolume 12, Article number: 176 (2017)
To determine the potential role of 68Ga-PSMA positron emission tomography/computed tomography (PET/CT) in radiotherapy (RT) planning for prostate cancer (PCa).
One hundred twenty-nine patients (pts) with 68Ga-PSMA PET/CT were retrospectively analysed. Potentially influencing factors (androgen deprivation therapy, amount of 68Ga-PSMA-HBED-CC, PSA doubling time ≤/> 10 months, PSA before PET/CT, T−/N-category and Gleason score) were evaluated by logistic regression analysis. The detection rate of PSMA PET/CT was compared to contrast enhanced CT and its impact on RT management analysed.
One hundred twenty-nine patients (pts) (20 at initial diagnosis, 49 with PSA relapse and 60 with PSA persistence after radical prostatectomy) received PSMA PET/CT prior to RT. The majority of pts. (71.3%) had PET-positive findings (55.1% of pts. with PSA recurrence, 75% of pts. with PSA persistence and 100% of newly diagnosed pts). Median PSA before PET/CT in pts. with pathological findings (n = 92) was 1.90 ng/ml and without (n = 37) 0.30 ng/ml. PSA level at time of PET/CT was the only factor associated with PET-positivity. In pts. with a PSA ≤ 0.2 ng/ml, the detection rate of any lesion was 33.3%, with a PSA of 0.21–0.5 ng/ml 41.2% and with a PSA of 0.51–1.0 ng/ml 69.2%, respectively. Regarding the anatomic distribution of lesions, 42.2% and 14.7% of pts. with relapse or persistence had pelvic lymph node and distant metastases. In pts. at initial diagnosis the detection rate of pelvic lymph nodes and distant metastases was 20% and 10%. 68Ga-PSMA PET/CT had a high detection rate of PCa recurrence outside the prostatic fossa in pts. being considered for salvage RT (22.4% PET-positive pelvic lymph nodes and 4.1% distant metastases). Compared to CT, PSMA PET/CT had a significantly higher sensitivity in diagnosing rates of local recurrence/primary tumour (10.1% vs. 38%), lymph nodes (15.5% vs. 38.8%) and distant metastases (5.4% vs. 14.0%). This resulted in a modification of RT treatment in 56.6% of pts.
The detection of PCa is strongly associated with PSA level at time of 68Ga-PSMA PET/CT. PSMA PET/CT differentiates between local, regional and distant metastatic disease with implications for disease management. PSMA PET/CT allows for tumour detection in post-prostatectomy pts. with PSA ≤ 0.5 ng/ml considered for salvage RT.
A precise detection and visualisation of disease extent is of essential importance for indication and target volume definition in radiotherapy of prostate cancer. Due to limitations in sensitivity and specificity, MRI and choline PET/CT are not considered precise enough especially at PSA levels ≤1 ng/ml [1, 2], although both imaging modalities are as well capable of modifying treatment approaches [3,4,5,6,7]. Recently, a 68Ga-labelled PSMA-targeted ligand with high affinity to prostate-specific membrane antigen (PSMA), a cell surface protein overexpressed in prostate cancer cells has been introduced for positron emission tomography (PET) imaging [8,9,10,11]. PET with 68Ga-PSMA demonstrated a superior tumour-to-background signal intensity and substantially higher detection rates than have been previously reported for other imaging modalities in patients with newly diagnosed [12,13,14,15] or recurrent [3, 16,17,18,19,20] prostate cancer. From surgical series, it is known that 68Ga-PSMA positron emission tomography/computed tomography (PET/CT) allows for a highly correct identification of lymph node metastases with a sensitivity and specificity ranging from 66% to 84% and 82% to 99% [14, 15], respectively. However, there is a substantial percentage of prostate cancer patients with a negative 68Ga-PSMA PET/CT. Bearing this in mind, we tried to determine retrospectively which factors correlate with a positive 68Ga-PSMA PET/CT in patients with primary, persistent or recurrent prostate cancer. Furthermore, we compared the detection rate of 68Ga-PSMA PET/CT to contrast enhanced CT and analysed its impact on the decision-making process within our department of radiation oncology. Several clinical scenarios may be distinguished: A PET-positive local recurrence within the prostatic fossa might justify a simultaneous integrated boost and an additional antiandrogen therapy. Likewise, PET-positive pelvic lymph node metastases might be treated with an enlargement of the clinical target volume, a focally higher dose and antiandrogen therapy. In addition, the evidence of distant metastases might even cause a non-realisation of a planned radiotherapy treatment.
68Ga-PSMA PET/CT has been routinely offered to patients for prostate cancer staging before radiotherapy in our clinic (February 2014–August 2016). A total of 129 patients consecutively received 68Ga-PSMA PET/CT prior to radiotherapy in different clinical scenarios: 20 patients at initial diagnosis (mostly high-risk patients with suspected extra-prostatic manifestations), 60 with biochemical persistence after radical prostatectomy and 49 with biochemical relapse (Table 1). All patients gave written informed consent to undergo 68Ga-PSMA PET/CT. This retrospective analysis is in compliance with the principles of the Declaration of Helsinki and its subsequent amendments  and was approved by the Ethics Committee of the LMU Medical Faculty .
PSMA ligand and PET/CT imaging
PSMA-HBED-CC was radiolabelled with 68Ga3+ from a 68Ge/68Ga generator system (GalliaPharm®, Eckert & Ziegler AG, Berlin, Germany) using an automated synthesis module (GRP, Scintomics GmbH, Munich, Germany) and pre-packed cassettes (ABX GmbH, Radeberg, Germany) as described previously for a different PSMA ligand by Weineisen et al. . 68Ga-PSMA PET/CT images extending from the base of the skull to the mid-thigh were acquired. PET/CT scan was obtained with intravenous injection of iodine-containing contrast agent (Ultravist 300, Schering, Berlin, Germany; or Imeron 300, Bracco, Konstanz; 2.5 mL/s; in portal venous phase) 60 min after almost simultaneous intravenous administration of 20 mg furosemide and 68Ga-PSMA (median 189 megabecquerel (MBq), range 87–293). Directly prior to the PET/CT scan, patients were asked to empty their bladder to minimise tracer accumulation.
PET/CT was interpreted by a consensus read of one nuclear medicine physician and one radiologist. Location of lesions was each determined by CT. PET-positive lesions were identified by 68Ga-PSMA uptake visually above background and not associated with the physiologic uptake. CT-positive nodes were defined by increased short axis diameter, loss of fatty hilum, or increased contrast enhancement. Bone metastases were detected by suspicious sclerotic lesions, visceral metastases by suspicious hypodense or hyperdense lesions in the respective organ. Based on PET/CT images and reports, stage according to PET or CT was documented separately by one nuclear medicine physician and one radiation oncologist .
Demographic and tumour characteristics were analysed. The association between positive 68Ga-PSMA PET/CT findings and possibly interacting variables, like androgen deprivation therapy (ADT) at the time of PET/CT, amount of injected tracer, PSA-level, PSA doubling time, T−/N-category and Gleason score was assessed by univariate and multivariate logistic regression analysis. P values <0.05 were considered statistically significant. PSA before PET/CT was classified in eight steps (≤ 0.2 ng/ml – > 20 ng/ml). Gleason score was grouped in six different classes (GS 5/6, GS 7a, GS 7b, GS 8, GS 9 and GS 10), T-category in four (T1 – T4) and N-category in three classes (N0, N1, Nx). Injected tracer amount was evaluated as multiples of 100 MBq. Patients after radical prostatectomy were classified by PSA doubling time ≤ vs. > 10 months. PET/CT positive findings (primary tumour/local recurrence, lymph node and distant metastases) are presented separately according to the respective treatment indication prior to radiotherapy. The detection rate of residual tumour, recurrence or newly diagnosed disease comparing PET/CT to CT exclusively as well as change in radiotherapy management was analysed by Fisher’s test.
A total of 129 patients (20 at initial diagnosis, 60 with biochemical persistence and 49 with biochemical relapse after radical prostatectomy) consecutively received 68Ga-PSMA PET/CT prior to radiotherapy (Table 1). Most patients (71.3%) had 68Ga-PSMA PET/CT-positive findings: Patients with biochemical recurrence had the lowest detection rate (55.1%) followed by patients with biochemical persistence (75%). At initial diagnosis, all patients (100.0%) had 68Ga-PSMA PET/CT-positive findings. Overall, the predominant GS, T- and N-category were 7b, T3 and N0 – in newly diagnosed patients prior to definitive radiotherapy 7b, cT1/cT3 and cN0, in patients with biochemical relapse 7a, pT2 and pN0 and in patients with biochemical persistence 9, pT3 and pN1, respectively. Altogether, most patients had a high-risk prostate cancer (79.8%) according to D’Amico risk group classification . PSA doubling time in post-prostatectomy patients differed between patients with biochemical recurrence having mainly a PSA doubling time > 10 months (57.1%) versus patients with biochemical persistence having a PSA doubling time ≤ 10 months (100%). ADT was in use in 14 patients at the time of 68Ga-PSMA PET/CT. Median PSA before 68Ga-PSMA PET/CT was 12.4 ng/ml in newly diagnosed patients, 0.99 ng/ml in patients with biochemical persistence and 0.49 ng/ml in patients with biochemical recurrence.
Factors predicting 68Ga-PSMA PET/CT positive findings
Patients with pathological radiotracer uptake (n = 92; Table 2) had a median PSA of 1.90 ng/ml (range 0.14–150.0), a PSA doubling time of mainly ≤10 months (77.8%), mainly a T3 N0 prostate cancer, a predominant GS 9 (29.3%) and ongoing ADT at time of PET in 12 patients. They were injected with a mean activity of 191.96 MBq 68Ga-PSMA-HBED-CC (range 87–293) and were mainly high-risk patients (81.5%). Patients without pathological findings (n = 37; Table 2) had a median PSA of 0.30 ng/ml (range 0.13–3.24), a PSA doubling time of mainly ≤10 months (67.6%), mainly a T3 N0 prostate cancer and a predominant GS 7b. Mean activity of 68Ga-PSMA-HBED-CC radiotracer was 186.78 MBq (range 94–293) in PET-negative patients with patients being mostly high-risk patients (75.7%) and two patients having ongoing ADT at the time of PET scan. In the univariate analysis (Table 3) no significant difference was found between PET-positive and PET-negative patients regarding the use of ADT at time of PET (p = 0.222), the injected amount of 68Ga-PSMA-HBED-CC (p = 0.590), the PSA doubling time ≤/> 10 months (p = 0.517), GS (p = 0.285) and T- (p = 0.982) and N-category (p = 0.987). Concerning PSA before PET, a significant difference was found (p < 0.001). In the multivariate analysis, the significant association between a PET-positive result and PSA level a time of PET persisted (p = 0.002). Figures 1 and 2 demonstrate the probability of pathological 68Ga-PSMA PET/CT depending on PSA level at time of PET/CT and GS. There is an almost linear increase of PET-positive result with rising PSA level: Patients with PSA ≤ 0.2 ng/ml had a detection rate of 33.3%, patients with PSA 0.21 ≤ 0.5 ng/ml a rate of 41.2% and patients with PSA 0.51 ≤ 1.0 ng/ml a rate of 69.2%.
Tumour location and PET versus CT-positive findings
Prior to definitive radiotherapy, 68Ga-PSMA PET/CT showed suspicious lesions within the prostate gland in 90% of patients and suspicious pelvic lymph nodes and/or distant metastases in 20%/10% of the patients, respectively. 68Ga-PSMA PET/CT had a high detection rate of prostate cancer recurrence outside the prostatic fossa in patients being considered for salvage radiotherapy: 22.4% of patients had PET-positive pelvic lymph nodes and 4.1% distant metastases. Both patients with distant metastases had also local recurrence exclusively without evidence of pelvic lymph node metastases. In patients considered for salvage radiotherapy with a PSA < 0.5 ng/ml (25 patients), 68Ga-PSMA PET/CT detected in 16.0% local recurrences within the prostatic fossa and in 20.0% PET-positive pelvic lymph nodes. In patients with postoperatively biochemical persistence, PET/CT revealed a high number of lymph node metastases (58.3%), distant metastases (23.3%) and macroscopic residual tumour (21.7%). Seventeen of 60 patients with persistent PSA after radical prostatectomy had a pre-PSMA PET/CT PSA <0.5 ng/ml. Of these patients, there was one patient (5.9%) with macroscopic residual tumour, 7 patients with pelvic lymph node metastases (41.2%) and 1 patient with distant metastases (5.9%). The single patient with bone metastases had pelvic lymph node involvement as well. Figure 3 shows a lesion based analysis of PET-positive local recurrence/primary tumour, PET-positive lymph node and distant metastases according to sub-grouping of patients and contains additional information on simultaneous involvement of local recurrent tumour/primary tumour, lymph node metastases and/or distant metastases. 68Ga-PSMA PET/CT as medical imaging modality had a significantly higher diagnostic value in the detection of suspicious lesions within the prostate/prostatic fossa (38% vs. 10.1%; p < 0.05), of suspicious pelvic lymph nodes (38.8% vs. 15.5%; p < 0.05) and distant metastases (14.0% vs. 5.4%; p < 0.05) compared to the contrast enhanced CT scan acquired during PET/CT imaging. This resulted in a modification of radiotherapy treatment in 56.6% of patients by e.g. enlarged target volumes or simultaneously integrated boost volumes. Figure 4 demonstrates the integration of 68Ga-PSMA PET/CT images into radiation therapy planning in three patients.
This heterogeneous group of patients with primary, recurrent or persistent prostate cancer represents a typical cohort referred to radiation oncology departments. We are thus confident that our findings are of relevance in clinical practice.
In general, out of 129 patients with high-risk primary, persistent or recurrent prostate cancer, PSMA-PET revealed a least one relevant lesion in 71.3% of the cohort. This rate compares nicely to the number of PET-positive patients (82.8%) in the study of Afshar-Oromieh et al. : a similarly heterogeneous group of patients with progressive disease after initial treatment (e.g. radiotherapy and/or surgery; n = 292), before initiation of local therapy (n = 27) or before therapy with radiolabelled PSMA ligands (n = 38) was analysed.
The clear correlation of PSA level and probability of detection was seen in our analysis (Fig. 1) as well as in the data provided by Ceci et al.  (n = 70), Afshar-Oromieh et al.  (n = 292) and Eiber et al. . Accordingly, patients with biochemical recurrence having the lowest PSA levels prior to PSMA PET/CT had the lowest detection rate (55.1%) compared to patients with persistent (75%) or primary prostate cancer (100%).
At present, PSA levels ≤0.2 ng/ml are frequently judged in postoperative patients to be non-critical, nevertheless one-third of our patients (33.3%) had PET-positive findings even below a PSA of 0.2 ng/ml. This rate drastically increased up to 69.2% in patients with a PSA level between 0.51–1.0 ng/ml. Thus, PSMA PET/CT detects early local recurrence or metastatic disease and possibly allows for a more effective and early treatment.
Apart from PSA-level before PET/CT, multivariate analysis detected no significant associations between a positive PSMA PET/CT and any of the other factors including ADT, amount of injected tracer, PSA doubling time, and Gleason score. This finding is well in accordance with the observations provided by Afshar-Oromieh et al.  regarding PSA doubling time and Gleason score. In contrast, Afshar-Oromieh et al. reported a positive association between detection rate and ongoing ADT. In animal models and in vitro cell culture experiments, ADT increases PSMA expression which might contribute to improved detection rate by 68Ga-PSMA PET/CT [26,27,28,29,30]. However, at present the complex association between an ADT driven increase of PSMA uptake in the individual tumour lesion, the ADT driven reduction of global tumour load and the final PET signal is not completely understood. In our opinion, the use of ADT in a cohort with mostly high-risk prostate cancer patients as evaluated by Afshar-Oromieh et al. is also a surrogate for high tumour burden and high PSA levels. We therefore counsel our patients to start with ADT after PSMA PET/CT if planned. Unlike the aforementioned trials, Ceci et al. also observed a significant association between PSA doubling time and PSMA PET/CT positivity . This might be explained by the fact that Ceci et al. coded PSA doubling time as continuous variables whereas in our trial and the trial of Afshar-Oromieh et al. PSA doubling time was analysed in distinct categories.
Compared to CT, sensitivity of PSMA PET/CT was significantly higher for local findings (38.0% vs. 10.1%), pelvic lymph nodes (38.8% vs. 15.5%) and distant failure (14.0% vs. 5.4%). This observation perfectly mirrors the findings reported by Giesel el al. showing that PSMA PET/CT is significantly more sensitive than CT-based 3D–volumetric lymph node evaluation .
Furthermore, we analysed the question how far an increased detection rate leads to a change in therapeutic management. In our series, PSMA PET/CT-positive findings had a substantial influence on the therapeutic concept in 56.6% of the patients with implication on either adaptation of treatment volumes, dose concepts or the commencement of hormone ablation therapy. This compares nicely to similar analyses [19, 31,32,33] all reporting major modifications of therapeutic management in 33.3% - 53.7% of the patients.
At present, PSMA PET/CT is widely regarded as the best modality for lymph node staging in a primary as well as in a postoperative setting [14, 34]. Data provided by van Leeuwen et al.  suggest that the level of lymph node positivity has been strongly underestimated in the pre-PSMA PET/CT era. In their analysis, lymphatic recurrences outside the prostatic fossa occurred in 20% of patients scheduled for salvage radiotherapy with additional 10% of distant metastases detected in PSMA PET/CT. Bearing in mind that currently only target volumes covering the prostatic fossa are routinely employed , a substantial rate of lymph node metastases is not treated. This is supported by our own data showing that even below a PSA level of 0.5 ng/ml, PSMA PET/CT still detected 20.0% of pelvic lymph node metastases in patients with salvage radiotherapy indication.
The documented need to treat PSA relapses as early as possible (even below PSA levels of 0.2 ng/ml) and the fact that the diagnostic sensitivity is optimal above a PSA level of 0.5 ng/ml currently creates an inherent dilemma. Since all data available consistently document that PSA control is significantly better when radiotherapy is commenced as early as possible [36, 37], it is not justified to wait until PSA is in an optimal diagnostic range. Our strategy to cope with this dilemma is therefore to employ PSMA PET/CT in patients even around 0.2 ng/ml especially whenever high-risk features are present. Like the analysis by Henkenberens et al. on 29 patients with biochemical recurrence receiving an individualized radiotherapy treatment plan based on PSMA PET/CT findings , target volumes are modified accordingly in our institution after critical assessment. Nevertheless, keeping the sensitivity and specificity rates from surgical series in mind, PSMA PET/CT might still underestimate the true extent of disease and should therefore from our point of view not result in an omission of nomogram  triggered radiotherapy treatment volumes.
At present, legal constraints prohibit the use of PSMA in truly prospective studies in Germany. Despite the clear limitations of retrospective approaches, the available data from several analyses strongly underline the high value of PSMA-PET/CT for staging as well as for treatment stratification in patients with primary high-risk, persistent or recurrent carcinoma of the prostate.
In this retrospective study, we showed that the detection of prostate cancer is strongly associated with PSA level at time of Ga-PSMA PET/CT. Better than any other imaging modality, PSMA PET/CT differentiates local, regional and distant metastatic disease with considerable implications for disease management. In post-prostatectomy patients with rising PSA ≤ 0.5 ng/ml with indication for salvage radiotherapy, PSMA PET/CT is narrowing the diagnostic gap as until now the gradual PSA increase often occurred long before recurrent disease could be localized clinically or by imaging.
androgen deprivation therapy
positron emission tomography
positron emission tomography/computed tomography
prostate-specific membrane antigen
Heidenreich A, Bastian PJ, Bellmunt J, Bolla M, Joniau S, van der Kwast T, et al. EAU guidelines on prostate cancer. Part II: treatment of advanced, relapsing, and castration-resistant prostate cancer. Eur Urol. 2014;65(2):467–79.
Schiller K, Sauter K, Dewes S, Eiber M, Maurer T, Gschwend J, Combs SE, et al. Patterns of failure after radical prostatectomy in prostate cancer - implications for radiation therapy planning after (68)Ga-PSMA-PET imaging. Eur J Nucl Med Mol Imaging. 2017; doi: 10.1007/s00259-017-3746-9.
Afshar-Oromieh A, Zechmann C, Malcher A, Eder M, Eisenhut M, Linhart H, et al. Comparison of PET imaging with a 68Ga-labelled PSMA ligand and 18F-choline-based PET/CT for the diagnosis of recurrent prostate cancer. EJNMMI. 2014;41(1):11–20.
Vargas HA, Martin-Malburet AG, Takeda T, Corradi RB, Eastham J, Wibmer A, et al. Localizing sites of disease in patients with rising serum prostate-specific antigen up to 1 ng/ml following prostatectomy: how much information can conventional imaging provide? Urol Oncol-Semin Orig Investig. 2016;34(11):482.e485-482.e410.
Panje C, Panje T, Putora PM, Kim SK, Haile S, Aebersold DM, et al. Guidance of treatment decisions in risk-adapted primary radiotherapy for prostate cancer using multiparametric magnetic resonance imaging: a single center experience. Radiat Oncol. 2015;10(1):47.
Hernandez D, Salas D, Giménez D, Buitrago P, Esquena S, Palou J, et al. Pelvic MRI findings in relapsed prostate cancer after radical prostatectomy. Radiat Oncol. 2015;10(1):262.
Gupta M, Choudhury PS, Hazarika D, Rawal SA. Comparative study of (68)gallium-prostate specific membrane antigen positron emission tomography-computed tomography and magnetic resonance imaging for lymph node staging in high risk prostate cancer patients: an initial experience. World J Nucl Med. 2017;16(3):186–91.
Afshar-Oromieh A, Malcher A, Eder M, Eisenhut M, Linhart HG, Hadaschik BA, et al. PET imaging with a 68Ga-labelled PSMA ligand for the diagnosis of prostate cancer: biodistribution in humans and first evaluation of tumour lesions. EJNMMI. 2013;40:797–8.
Eder M, Schafer M, Bauder-Wust U, Hull WE, Wangler C, Mier W, et al. 68Ga-complex lipophilicity and the targeting property of a urea-based PSMA inhibitor for PET imaging. Bioconjug Chem. 2012;23:688–97.
Sweat SD, Pacelli A, Murphy GP, Bostwick DG. Prostate-specific membrane antigen expression is greatest in prostate adenocarcinoma and lymph node metastases. Urology. 1998;52:637–40.
Silver DA, Pellicer I, Fair WR, Heston WD, Cordon-Cardo C. Prostate-specific membrane antigen expression in normal and malignant human tissues. Clin Cancer Res. 1997;3(1):81–5.
Fendler WP, Schmidt DF, Wenter V, Thierfelder KM, Zach C, Stief C, et al. 68Ga-PSMA-HBED-CC PET/CT detects location and extent of primary prostate cancer. J Nucl Med. 2016;57:1720–5.
Eiber M, Weirich G, Holzapfel K, Souvatzoglou M, Haller B, Rauscher I, et al. Simultaneous (68)Ga-PSMA HBED-CC PET/MRI improves the localization of primary prostate cancer. Eur Urol. 2016;70(5):829–36.
Maurer T, Gschwend JE, Rauscher I, Souvatzoglou M, Haller B, Weirich G, et al. Diagnostic efficacy of (68)Gallium-PSMA positron emission tomography compared to conventional imaging for lymph node staging of 130 consecutive patients with intermediate to high risk prostate cancer. J Urol. 2016;195(5):1436–43.
Herlemann A, Wenter V, Kretschmer A, Thierfelder KM, Bartenstein P, Faber C, et al. (68)Ga-PSMA positron emission tomography/computed tomography provides accurate staging of lymph node regions prior to lymph node dissection in patients with prostate cancer. Eur Urol. 2016;70:553–7.
Afshar-Oromieh A, Avtzi E, Giesel F, Holland-Letz T, Linhart H, Eder M, et al. The diagnostic value of PET/CT imaging with the 68Ga-labelled PSMA ligand HBED-CC in the diagnosis of recurrent prostate cancer. EJNMMI. 2015;42(2):197–209.
Eiber M, Maurer T, Souvatzoglou M, Beer AJ, Ruffani A, Haller B. Evaluation of hybrid 68Ga-PSMA-Ligand PET/CT in 248 patients with biochemical recurrence after radical prostatectomy. J Nucl Med. 2015;56:668–74.
Giesel F, Fiedler H, Stefanova M, Sterzing F, Rius M, Kopka K, et al. PSMA PET/CT with Glu-urea-Lys-(Ahx)-[68Ga(HBED-CC)] versus 3D CT volumetric lymph node assessment in recurrent prostate cancer. EJNMMI. 2015;42(12):1794–800.
van Leeuwen PJ, Stricker P, Hruby G, Kneebone A, Ting F, Thompson B, et al. (68) Ga-PSMA has a high detection rate of prostate cancer recurrence outside the prostatic fossa in patients being considered for salvage radiation treatment. BJU Int 2016; 117(5):732-739.
Afshar-Oromieh A, Holland-Letz T, Giesel FL, Kratochwil C, Mier W, Haufe S, et al. Diagnostic performance of (68)Ga-PSMA-11 (HBED-CC) PET/CT in patients with recurrent prostate cancer: evaluation in 1007 patients. EJNMMI. 2017;44(8):1258–68.
General Assembly of the World Medical Association. World medical association declaration of Helsinki: ethical principles for medical research involving human subjects. J Am Coll Dent. 2014;81(3):14–8.
Weineisen M, Simecek J, Schottelius M, Schwaiger M, Wester H-J. Synthesis and preclinical evaluation of DOTAGA-conjugated PSMA ligands for functional imaging and endoradiotherapy of prostate cancer. EJNMMI Res. 2014;4(1):1–15.
Clinical Practice Guidelines in Oncology: Prostate Cancer. V.1.2015. http://www.nccn.org/professionals/physician_gls/pdf/prostate.pdf. Accessed 30 Dec 2015.
D’Amico AV, Whittington R, Malkowicz SB, Weinstein M, Tomaszewski JE, Schultz D, et al. Predicting prostate specific antigen outcome preoperatively in the prostate specific antigen era. J Urol. 2001;166:2185–8.
Ceci F, Uprimny C, Nilica B, Geraldo L, Kendler D, Kroiss A, et al. (68)Ga-PSMA PET/CT for restaging recurrent prostate cancer: which factors are associated with PET/CT detection rate? EJNMMI. 2015;42(8):1284–94.
Evans MJ, Smith-Jones PM, Wongvipat J, Navarro V, Kim S, Bander NH, Larson SM, et al. Noninvasive measurement of androgen receptor signaling with a positron-emitting radiopharmaceutical that targets prostate-specific membrane antigen. Proc Natl Acad Sci. 2011;108(23):9578–82.
Murga JD, Moorji SM, Han AQ, Magargal WW, DiPippo VA, Olson WC. Synergistic co-targeting of prostate-specific membrane antigen and androgen receptor in prostate cancer. Prostate. 2015;75(3):242–54.
Liu T, Wu LY, Fulton MD, Johnson JM, Berkman CE. Prolonged androgen deprivation leads to downregulation of androgen receptor and prostate-specific membrane antigen in prostate cancer cells. Int J Oncol. 2012;41(6):2087–92.
Hope TA, Truillet C, Ehman EC, Afshar-Oromieh A, Aggarwal R, Ryan CJ, et al. 68Ga-PSMA-11 PET imaging of response to androgen receptor inhibition: first human experience. J Nucl Med. 2017;58(1):81–4.
Wright GL Jr, Mayer Grob B, Haley C, Grossman K, Newhall K, Petrylak D, et al. Upregulation of prostate-specific membrane antigen after androgen-deprivation therapy. Urology. 1996;48(2):326–34.
Shakespeare TP. Effect of prostate-specific membrane antigen positron emission tomography on the decision-making of radiation oncologists. Radiat Oncol. 2015;10(1):1–4.
Dewes S, Schiller K, Sauter K, Eiber M, Maurer T, Schwaiger M, et al. Integration of (68)Ga-PSMA-PET imaging in planning of primary definitive radiotherapy in prostate cancer: a retrospective study. Radiat Oncol. 2016;11:73.
Sterzing F, Kratochwil C, Fiedler H, Katayama S, Habl G, Kopka K, et al. 68Ga-PSMA-11 PET/CT: a new technique with high potential for the radiotherapeutic management of prostate cancer patients. EJNMMI. 2015:1–8.
Perera M, Papa N, Christidis D, Wetherell D, Hofman MS, Murphy DG, et al. Sensitivity, specificity, and predictors of positive 68Ga-prostate-specific membrane antigen positron emission tomography in advanced prostate cancer: a systematic review and meta-analysis. Eur Urol. 2016;70(6):926–37.
Bell LJ, Cox J, Eade T, Rinks M, Herschtal A, Kneebone A. Determining optimal planning target volume and image guidance policy for post-prostatectomy intensity modulated radiotherapy. Radiat Oncol. 2015;10(1):151.
Tendulkar RD, Agrawal S, Gao T, Efstathiou JA, Pisansky TM, Michalski JM, et al. Contemporary update of a multi-institutional predictive Nomogram for salvage radiotherapy after radical prostatectomy. J Clin Oncol. 2016;34(30):3648–54.
Pfister D, Bolla M, Briganti A, Carroll P, Cozzarini C, Joniau S, et al. Early salvage radiotherapy following radical prostatectomy. Eur Urol. 2014;65(6):1034–43.
Henkenberens C, von Klot CA, Ross TL, Bengel FM, Wester HJ, Merseburger AS, et al. (68)Ga-PSMA ligand PET/CT-based radiotherapy in locally recurrent and recurrent oligometastatic prostate cancer : early efficacy after primary therapy. Strahlenther Onkol 2016; 192(7):431-439.
Wu R, Woodford H, Capp A, Hunter P, Cowin G, Tai K-H, et al. A prospective study of nomogram-based adaptation of prostate radiotherapy target volumes. Radiat Oncol. 2015;10(1):243.
No funding was received.
Availability of data and materials
The datasets used and analysed during the current study are available from the corresponding author on reasonable request.
Ethics approval and consent to participate
All patients gave written consent to undergo 68Ga-PSMA PET/CT. This retrospective analysis is in compliance with the principles of the Declaration of Helsinki and its subsequent amendments  and was approved by the Ethics Committee of the LMU Medical Faculty.
Consent for publication
The authors declare that they have no competing interests.
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Nina-Sophie Schmidt-Hegemann and Wolfgang Peter Fendler are equal contributors.