Non-prostate cancer tumours: incidence on 18F-DCFPyL PSMA PET/CT and uptake characteristics in 1445 patients

Purpose With increasing use of PSMA PET/CT in the staging and restaging of prostate cancer (PCa), the identification of non-prostate cancer tumours (NPCaT) has become an increasing clinical dilemma. Atypical presentations of PSMA expression in prostate cancer and expression in NPCaT are not well established. Understanding the normal and abnormal distribution of PSMA expression is essential in preparing clinically relevant reports and in guiding multidisciplinary discussion and decisions. Methods Retrospective review of 1445 consecutive 18F-DCFPyL PSMA PET/CT studies by experienced radiologists and nuclear medicine physicians. Lesions indeterminate for PCa were identified. Correlation was made with patient records, biopsy results, and dedicated imaging. Lesions were then categorized into four groups: 1. Confirmed prostate cancer, metastases, 2. NPCaT 3. Benign, and 4. Indeterminate lesions. Results 68/1445 patients had lesions atypical for prostate cancer metastases. These comprised 8/68 (11.8%) atypical prostate cancer metastases, 17/68 (25.0%) NPCaT, 29/68 (42.6%) indeterminate, and 14/68 (20.6%) benign. In the context of the entire cohort, these are adjusted to 8/1445 (0.6%), 17/1445 (1.2%), 29/1445 (2.0%), and 14/1445 (1.0%) respectively. With the exception of Renal Cell Carcinoma (RCC), NPCaT demonstrated no or low PSMA expression. A similar trend was also observed for indeterminate and benign lesions. Conversely, most atypical PCa metastases demonstrated intermediate or high PSMA expression. Conclusion 18F-DCFPyL PSMA PET/CT detection of NPCaT is low. Lesions demonstrating intermediate to high PSMA expression were exclusively prostate cancer metastases, aside from RCC, and lesions detected in organs with high background expression. Supplementary Information The online version contains supplementary material available at 10.1007/s00259-022-05721-z.


Introduction
Prostate cancer (PCa) is the second most commonly diagnosed cancer in men and is the sixth leading cause of cancer death [1]. Imaging of prostate cancer both at initial staging and at recurrence has been revolutionized by the advent of positron emission tomography (PET) tracers targeted to prostate specific membrane antigen (PSMA) which have shown superiority in comparison with conventional imaging comprising CT and bone scintigraphy [2][3][4].
PSMA is a transmembrane glycoprotein with high expression in most prostate cancer cells although can be expressed in endothelial cells in non-prostate cancer tumours (NPCaT), particularly in the context of neovascularization [5]. There are several PSMA PET probes available, of which Gallium This article is part of the Topical Collection on Oncology -Genitourinary. 1 3 68 probes are most widely used. Newer Fluorine 18 probes confer some advantages with longer half-life, opportunity for large scale batch production, and higher target to background resolution. 18 F-DCFPyL is a commercially available PSMA PET probe used at our institutions.
This wide adoption of PSMA PET/CT with increasing availability of tracers has seen a substantial increase in its use which, along with expanding applications of PSMA in the realms of initial diagnosis, biochemical recurrence, and treatment follow-up, the identification of NPCaT is likely to increase accordingly. The physiological expression of PSMA, expression in benign pathology, and typical patterns of expression in prostate cancer are well documented [6]; however, atypical presentations of PSMA expression in prostate cancer and expression in NPCaT are less established. Understanding the normal and abnormal distribution of PSMA expression is essential in preparing clinically relevant reports and in guiding multidisciplinary discussion and decisions.
Our multicenter international retrospective study is designed to detect the incidence and types of NPCaT detected on 18 F-DCFPyL PSMA PET/CT in patients with PCa and describe their imaging characteristics. The primary outcome was the incidence of newly diagnosed NPCaT detected in this cohort. We also aimed to evaluate characteristics of atypical prostate cancer metastases and indeterminate lesions. Benign lesions outside the realms of abdominal incidentalomas and incidental lung nodules determined suitable for follow-up protocols were also examined.

Study population
Retrospective multicenter international study using combined data from Pacific Radiology Canterbury, New Zealand (PRC) and St Vincent's Hospital, Melbourne, Australia (STV). Institutional ethics approval has been granted for the maintenance of a prostate cancer database, from which the study data was derived. Our database includes consecutive patients who have had 18 F-DCFPyL PET/CT between January 2016 and December 2020. Repeat studies for the same patient were excluded. For patients with multiple studies, only the first showing a suspected NPCaT was included. The patient cohort consisted of patients having a 18 F-DCFPyL PET/CT for initial staging (35.6%), re-staging (5.1%), and biochemical failure post treatment (59.3%).

Case selection and imaging analysis
All imaging reports were reviewed to identify patients with suspected incidental NPCaT. Typical prostate cancer-related lesions were defined as PSMA expression greater than background in the expected distribution for prostate cancer within prostate/prostate bed, nodes, bone and visceral locations [6]. Typical sites of nodal involvement include obturator, iliac stations, and retroperitoneum. Although mesorectal nodes have been described as rare or atypical, these were included in the expected distribution as they are increasingly recognised. Distant nodal, liver, and thoracic metastases were also considered typical distributions. Although visceral metastases are described in the absence of nodal or bone involvement, extra-prostatic disease limited to these sites required clarification [6]. These studies were reviewed by either an experienced genitourinary radiologist with subspecialist PET/CT practice or an experienced genitourinary radiologist in consultation with an experienced nuclear medicine physician. Imaging features of the incidental lesions and standardized uptake values (SUVmax) were recorded and categorised according to PROMISE miPSMA expression score. Terminology used in this paper reflecting these guidelines were no expression (below blood pool, score 0), low expression (equal to or above blood pool and lower than liver, score1), intermediate expression (equal to or above liver and lower than parotid gland, score 2) or high expression (equal to or above parotid gland, score 3) [7]. Histology reports were obtained from medical records and pathologic databases, follow-up imaging from the institutional PACS database, and clinical management from the patient's medical records.
Non-avid incidental lung lesions were assessed by a chest radiologist with > 10 years' experience. Those less than 10 mm with no PSMA expression and without features suggesting atypical adenomatous hyperplasia/adenocarcinoma spectrum which fitted adopted follow-up guidelines were excluded [8,9]. Known lesions which had already been identified and investigated on prior imaging were also excluded.
Abdominal 'incidentalomas' with no PSMA expression, including adrenal adenomas, liver and renal cysts, were assessed by a subspecialist abdominal radiologist with > 10 years' experience and those fitting criteria for follow up under ACR white paper for follow-up of incidentalomas were recorded but excluded from end point analysis [10][11][12][13].
Patient records were retrieved and subsequent biopsy results, dedicated imaging, multidisciplinary team meeting notes, follow-up clinic letters, and specialist consults were noted. Based on this information in combination with imaging characteristics, lesions were categorized broadly into four groups: 1. confirmed prostate cancer metastases: lesions either in an atypical distribution for PCa and/or considered possible NPCaT, subsequently determined as PCa lesion by histological or clinical confirmation; 2. NPCaT: lesions either in an atypical distribution for PCa and/or considered possible NPCaT, subsequently determined as NPCaT by histological or clinical confirmation; 3. benign: lesions not excluded by lung nodule or incidentaloma criteria either in an atypical distribution for PCa and/or considered possible NPCaT, subsequently determined as benign by histological or clinical confirmation; and 4. indeterminate lesions: lesions not excluded by lung nodule or incidentaloma criteria either in an atypical distribution for PCa and/or considered possible NPCaT, without definitive histological or clinical confirmation. The lesions classified as indeterminate were sub-classified as a. likely benign and b. likely malignant. 18 F-DCPyL for both centres was sourced from Cyclotek (Melbourne, Australia and Wellington, New Zealand) produced by the same method described previously [14].

Imaging protocols and reconstruction
PRC: Patients were required to drink 1-2L of water prior to their appointment and void immediately prior to scanning. No diuretics were administered. Patients were imaged on a GE Discovery 690 (General Electric Medical Systems, Milwaukee WI, USA). Low-dose attenuation correction CT images were acquired and reconstructed to 3.75 mm slice thickness with an increment of 3.27 mm using iterative reconstruction (50% ASiR). All patients at both centres were administered 250 MBq (± 50 MBq) of 18F-DCFPyL intravenously in accordance with reference standards outlined by the Australian Radiation Protection and Nuclear Safety Agency (ARPANSA) [15]. Imaging was performed at 120 min (± 10 min) after injection. PET images were acquired at 3.5 min/bed through the pelvis and 3.0 min/bed to the lung apices. Images were reconstructed from time of flight emission data using VUE Point FX and Q-Clear™ "GE Healthcare" iterative technique with a β value of 400. Sharp IR function was applied with no Z-axis filter. PET images were reconstructed on a 256 matrix.
STV: Patients were imaged on a GE Discovery 710 PET/CT (General Electric Medical Systems, Milwaukee WI, USA). Otherwise the scanning protocol matched that described above.

Statistical analysis
PSMA and pathological findings were assessed using binomial categorical data from unmatched groups compared with a chi-square test. Statistical analyses were conducted with Jamovi software, version 1.2.22.0.

Results
A total of 1445 studies were performed using 18 F-DCFPyL (PRC = 865 studies, STV = 580 studies). One thousand two hundred forty-three of these studies were excluded as they had lesions typical for prostate cancer or no detectable lesion. Two hundred two studies remained for further analysis. Of these studies, 85 related to lung nodules and 49 to incidentalomas, fulfilling the exclusion criteria. Out of 49 incidentalomas, 23/49 (46.9%) were hepatic cysts or hemangiomas, 10/49 (20.4%) were adrenal adenomas, and 9/49 (18.4%) were renal cysts. The remaining 7/49 (14.3%) were made up of pancreatic cysts, subcutaneous nodule, bone island and incidental gastric mucosal thickening. A total of 68 studies were therefore included in our study (Fig. 1).
Within our cohort, the number of false positives included 24/68 (35.3%) patients, who had avid lesions that were proven to be benign either clinically or through biopsy. In the context of the entire cohort, this adjusted to 24/1445 (1.7%) patients.

Confirmed prostate cancer metastases
5/8 (62.5%) of lesions subsequently confirmed as prostate cancer metastases demonstrated intermediate to high PSMA expression, 4 of which were lung metastases, with biopsy confirmation, and one biopsy confirmed nodal metastasis. The remaining 3/8 (37.5%) lesions were of low or no expression comprising two lung and one bone metastasis demonstrating a range of PSMA expression from SUVmax of < 1 to 5.3 (Table 1).

Non-prostate cancer tumours
17/68 (25.0%) patients within our cohort had NPCaT. 2/17 (11.8%) lesions demonstrated intermediate to high heterogeneous PSMA expression and characteristic CT features of renal cell carcinoma (RCC). The remaining 15/17 (88.2%) lesions had no or low PSMA expression. Twelve of these were classified as tumours with high malignant potential and the remaining 3 as low malignant potential.
PSMA and pathological findings of NPCaT in our cohort have been summarized in Table 2. 8/17 (47.1%) of these patients were non-biopsy diagnoses. This was either based on PSMA findings or subsequent imaging displaying characteristic findings of non-prostate cancer; however, in some patients, this diagnosis was made by multidisciplinary consensus as further imaging or biopsy was not felt clinically appropriate due to advanced patient age, performance status or widespread metastatic malignancy. 9/17 (52.9%) patients had biopsy confirmation. Three of these patients had lung lesions, all of which were biopsy-proven primary lung cancer. Two patients had focal low PSMA expression within the colon, both of which had biopsy-proven colonic adenocarcinoma, one of which had additional biopsies confirming synchronous neuroendocrine tumor within the terminal ileum, occult on PET/CT.
Histopathological assessment of a breast lesion with low PSMA expression (SUVmax 2.8) was proven to be a recurrent ER positive grade 2 breast invasive carcinoma. The remaining three had histopathology consistent with clear cell RCC with no PSMA expression (SUVmax < 1), poorly differentiated pancreatic adenocarcinoma with low PSMA expression (SUVmax 4.8), and follicular lymphoma with low PSMA expression (SUVmax 3.5). 25

Benign lesions
Most benign lesions were within the thyroid (6/14) and skin (4/14). 10/14 cases were biopsy proven and 4/14 cases were clinically proven benign lesions. All lesions except a scrotal lesion demonstrated no or low PSMA expression (Table 4).

Discussion
This study represents the largest cohort to date assessing incidence of NPCaT detected by PSMA imaging and is the only study exclusively examining this incidence with 18 F-DCFPyL PET/CT. PSMA imaging is considered highly    showed granulomatous epididymitis specific for prostate cancer although this specificity is only realized in combination with a comprehensive knowledge of the physiological and abnormal expression of PSMA. Physiological expression and distribution of typical prostate cancer related abnormal expression is well documented. [6] Atypical PCa metastases are seen in less than 5% of cases but can affect most organs. Atypical metastases are rare in isolation and are often observed in the context of a typical pattern of disseminated metastatic PSMA expressing PCa. In addition, PCa metastases are described as focal with high PSMA expression whereas NPCaT expression is more likely to be low and non-focal [6,16]. All lesions in our cohort categorized as PCa metastases were in expected sites for metastatic disease but NPCaT required exclusion due to their structural features or clinical presentation ( were more likely to be PCa metastases rather than NPCaT regardless of their CT morphology. All of the NPCaT in our group (except for two RCC cases) demonstrated no or low PSMA expression (SUV < 5). These findings correlate with literature describing PSMA expression in RCC [17,18]. Although some cases in our cohort were not followed up due to factors including patient age, comorbidity, and extensive tumour burden, many lesions were subject to MDM discussion, clinical and radiological follow-up, and/or biopsy. This approach is valid and necessary in the clinical workup of these patients particularly in the context of advancing treatment options for patients with oligometastatic disease.
Numerous benign lesions are also known to express PSMA; however, from our cohort, the indeterminate and benign lesions largely demonstrated no or low PSMA expression (SUVmax < 5) [16,19]. Pulmonary nodules in this patient cohort were common and the majority were assigned to follow-up based upon established guidelines [8,9]. Lung nodules comprised the majority of the incidental potentially malignant group although these were larger (11-40 mm) with more complex imaging features and some demonstrated low PSMA expression. We found that lung nodules with intermediate or high PSMA expression were exclusively PCa metastases in our cohort whereas no biopsy-proven lung cancer demonstrated intermediate or high PSMA expression, despite PSMA expression in lung cancer described in the literature [20]. Our study has demonstrated that PCa metastases are substantially more frequent than NPCaT in the context of thoracic lesions with intermediate to high PSMA expression. These findings are further substantiated when considered in the context of existing structured reporting systems. For example, the European Association of Nuclear Medicine, including authors of both PROMISE data and PSMA-RADS, has recently provided guidelines for standardised reporting using E-PSMA fivepoint scale. The majority of the indeterminate and NPCaT lesions in our cohort comply with category 3 E-PSMA (indeterminate) lesions and the majority of benign lesions correspond to category 2 E-PSMA (likely benign). Furthermore, many lesions later confirmed to be PCa metastases arguably fell under E-PSMA 5, which would correctly allocate them to PCa metastases, but additional findings beyond this definition prompted clinical uncertainty, such as morphology, solitary site of disease, and other malignancy and predisposing factors for second primary [7,21,22].
The ability to differentiate PCa metastases from NPCaT is vital as further investigation can lead to morbidity, delays in therapy and incurs additional medical costs. In our cohort, 8% of patients with benign incidental findings underwent a biopsy as part of further investigation while of 19 patients with lung nodules over 10 mm, 13 (68%) were biopsied. Recognizing these patterns in context of established standardised reporting criteria can give PET/CT specialists the ability to make a confident diagnosis, thus avoiding escalating investigation, cost and therapeutic delays [7]. Importantly we would emphasise that guidelines and structured reporting systems allow for reduced variation of interpretation and clear communication however overall interpretation critically relies upon multiple factors and a multidisciplinary approach to diagnosis and management is paramount [7,22].
The incidence of NPCaT in our PSMA cohort (1.7%) is substantially less than the incidence of significant incidental non-FDG avid findings on FDG PET/CT (22.6%) [23]. There are a number of potential reasons for this, including differing demographics, definitions of 'major' clinical significance, stricter evidence-based criteria used in our study, the use of subspecialist radiologists to exclude benign pathologies along with our exclusion of pre-existing known pathologies.
PSMA expression in NPCaT is more commonly associated with tumours which undergo neovascularization such as RCC, breast, glial tumours, gastrointestinal, pancreatic and lung tumours, all of which were represented in our cohort [24][25][26][27][28][29]. Further tumours reported to express PSMA not represented in our study include oral SCC, salivary ductal carcinoma, medullary thyroid carcinoma, small cell lung cancer, osteosarcoma, gynaecological malignancies, and adenoid cystic tumours [30,31]. Such expression is variable but has significant clinical implications. PSMA imaging may provide an investigative tool for such tumours, with particular recent interest in clear cell RCC and in detection and characterisation of metastatic diseases [18,[32][33][34][35]. The potential for PSMA targeted radiopharmaceuticals in non-prostate tumours is vast and the degree of PSMA expression may prospectively select treatment candidates and monitor response. Treatment monitoring, in particular drugs targeting neovascularization, e.g. bevacizumab and tyrosine kinase inhibitors, is a further potential application. PSMA expression in NPCaT may aid prognostication, for example, PSMA expression in non-metastatic triple negative breast cancer confers worse prognosis with higher relapse and reduced response to androgen receptor inhibition [25,30]. In contrast, PSMA expression in nonsmall cell lung cancer (NSCLC) is associated with earlier stage tumours. It is noteworthy that these concepts remain in the realm of research and the full clinical impact of these applications is yet to be determined [24,36].
This study benefited from a large number of consecutive patients in a multicenter international setting. A limitation of this study was its retrospective design. The largest impact of this was that many patients did not have histological confirmation and/or did not have conclusive follow up, leading to indeterminate findings in a cohort of patients. Selection of patients based on initial reports can introduce subjectivity and bias; however, the initial reports were generated by subspecialty trained experienced radiologists and nuclear medicine physicians. The imaging centers used different scanners albeit two consecutive generations of the same product, however this may have affected SUVmax measurements. Low numbers of individual non-prostate cancer tumours limit the ability to provide specific recommendations. There is always a degree of subjectivity when categorizing the significance of incidental findings and no perfect system exists although we have attempted to mitigate this by using experienced subspecialist radiologists and by considering the opinion of multidisciplinary meetings.

Conclusion
Our work is the largest study to date examining incidence of NPCaT detected by PSMA PET/CT and is the only study exclusively examining incidence in 18 F-DCFPyL PET/CT. PSMA imaging of PCa is highly specific with the detection of PSMA expressing NPCaT exceedingly rare. NPCaT in our cohort generally demonstrated low or no PSMA expression. Although PSMA expression was noted in RCC, this was lower and less focal than typical PCa metastatic disease. We found that significant PSMA expressions at sites typical for prostate cancer metastases were exclusively PCa metastases rather than NPCaT.
Funding Open Access funding enabled and organized by CAUL and its Member Institutions.

Data availability At request.
Code availability Not applicable.

Declarations
Ethics approval Formal ethics review was waived under the New Zealand Health and Disability Ethics Committee exemption for minimal risk retrospective observational studies. Australian data was collected with an ethics approved prostate cancer database.

Consent to participate Not applicable.
Consent for publication Not applicable.

Conflict of interest The authors declare no competing interests.
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