An overview on prostate-specific membrane antigen uptake in malignancies other than prostate cancer: A pictorial essay

Abstract

Prostate-specific membrane antigen (PSMA) is a Type II transmembrane glycoprotein which is extremely overexpressed in prostate cancer epithelial cells. Recently, PSMA-targeted small molecule labeled with ⁶⁸Ga and ^99mTc allowed precise molecular imaging of prostate cancer and PSMA-targeted small molecule labeled with 177Lu leads to the development of radionuclide-targeted therapy of prostate cancer. Despite its name, it has been shown that PSMA has been expressed in several malignancies which can be due to significant neovascularization. Present pictorial assay reports the nonspecific tracer uptake in some malignancies during ⁶⁸Ga-PSMA positron-emission tomography/computed tomography imaging and ^99mTc-PSMA scintigraphy.

Keywords

68Ga-prostate-specific membrane antigen positron-emission tomography/computed tomography - ^99mTc-prostate-specific membrane antigen scintigraphy - prostate cancer - prostate-specific membrane antigen and nonspecific uptake

Introduction

Prostate-specific membrane antigen (PSMA) is a Type II transmembrane glycoprotein which is extremely overexpressed in prostate cancer epithelial cells.[1] Higher tumor stage and grade, tumor dedifferentiation, hormone resistance, and metastatic disease lead to increase in overexpression of PSMA.[2] Although PSMA first was identified in the prostate gland, its expression in the duodenal epithelium, proximal tubule cells in the kidney, salivary glands, and tumor-associated vascular endothelium have been revealed in eventual histopathological studies.[3],[4],[5]

Recently, innovative development of PSMA-targeted small molecule labeled with ⁶⁸Ga and ^99mTc allowed precise molecular imaging of prostate cancer and PSMA-targeted small molecule labeled with ¹⁷⁷Lu led to the development of radionuclide-targeted therapy of prostate cancer.

⁶⁸Ga-PSMA positron-emission tomography (PET) since its first use in 2013 has revolutionized the management and imaging of patients with prostate cancer. Numerous studies have proved the high efficacy of ⁶⁸Ga-PSMA in diagnosing, staging, follow-up, restaging, and evaluating treatment response.[6],[7],[8],[9]

Regarding the cost benefits and broader availability of single-photon emission computed tomography (CT) compared to PET, ^99mTc-labeled small molecule inhibitor has been developed. The clinical evaluation and detection rate of ^99mTc-PSMA in staging, recurrence, and treatment response of patients with prostate cancer have been evaluated in previous studies.[10],[11],[12],[13] Schmidkonz et al.[13] used ^99mTc-MIP-1404 as a ^99mTc-labeled PSMA inhibitor for the detection of prostate cancer with biochemical recurrence. Tracer-positive lesions were detected in 77% of patients, which indicated that this radiotracer has a high probability in the management of prostate cancer patients with biochemical recurrence. In another study, Reinfelder et al.[14] evaluated the detection efficacy of ^99mTc-MIP-1404 in prostate cancer patients with biochemical recurrence. It has been reported that 70% of patients showed positive lesion which revealed that MIP-1404 is a promising radiotracer for the detection of prostate cancer lesions.

However, despite its name, in addition to prostate tissue, PSMA is physiologically expressed in a multiple number of nonprostatic malignancies because of PSMA mRNA transcripts and protein expression in the endothelium of tumor-related neovasculature, leading to potential pitfalls in the clinical use of PSMA-targeted imaging.[3],[4],[15] Nevertheless, PSMA expression in nonprostatic malignancies may prove beneficial in therapeutic and imaging targets for these conditions. [Table 1] represents malignancies other than prostate cancer which shows PSMA uptake in previous researches. In this pictorial assay, we reported a few nonprostatic malignancies cases, i.e., differentiated thyroid cancer, esophageal cancer, pancreaticobiliary adenocarcinoma, ureteral cancer, cholangiocarcinoma, pancreatoblastoma, hepatoblastoma, and carcinoma of unknown primary showing PSMA expression during ^99mTc/177Lu-PSMA scintigraphy and 68Ga-PSMA PET imaging [Figure 1], [Figure 2], [Figure 3], [Figure 4], [Figure 5], [Figure 6], [Figure 7], [Figure 8].

Table 1 Previous literatures on prostate-specific membrane antigen uptake in malignancies other than prostate cancer

Figure 1 A 54-year-old woman with differentiated thyroid cancer underwent ablation with radioiodine therapy. Posttreatment scan revealed just extensive uptake of I-131 in thyroid bed and did not show any remarkable uptake in the rest of the body. As the previous study indicated the Prostate-specific membrane antigen expression in differentiated thyroid cancer,[18],[20] ^99mTc-prostate-specific membrane antigen scintigraphy was done for disease assessment showing diffuse severe uptake in the lung (a). As mentioned in previous studies, [45],[46] currently, the therapeutic options are limited for patients with metastasized, ¹³¹I-resistant differentiated thyroid cancer, therefore, in another case, ^99mTc-prostate-specific membrane antigen scintigraphy was performed in a 40-year-old male with radioiodine refractory differentiated thyroid cancer. The scan showed a diffuse severe uptake of radiotracer in the lung (b). Therefore, such patients can be a candidate for novel therapy with ¹⁷⁷Lu-prostate-specific membrane antigen

Figure 2 ⁶⁸Ga-prostate-specific membrane antigen positron emission tomography/computed tomography was performed for a 71-year-old male with a history of prostate adenocarcinoma (GS: 4 + 5) underwent prostatectomy 6 years ago. One year after prostatectomy, due to local recurrence, the patient underwent second surgery, external beam radiation therapy and brachytherapy. Due to rising prostate-specific antigen, ⁶⁸Ga-prostate-specific membrane antigen positron-emission tomography/computed tomography was performed for recurrence evaluation. The scan revealed a mid-esophageal mass with esophageal stenosis and highly increased radiotracer uptake, suggesting a second primary cancer with mediastinal lymph nodes metastases. According to the prior studies, increased prostate-specific membrane antigen expression maybe due to significant neovascularization revealed in gastroesophageal cancers [21],[38]

Figure 3 ⁶⁸Ga-prostate-specific membrane antigen positron emission tomography/computed tomography was performed for a 46-year-old woman with a history of multiple hepatic lesions which on biopsy it was adenocarcinoma most likely pancreatobiliary underwent 7 courses of chemotherapy. The scan revealed a 54 mm × 39 mm mass lesion in the segment 5 liver with a maximum standardized uptake value of 11.32 corresponding to the recently computed tomography and fluorodeoxyglucose-positron emission tomography/computed tomography finding. The fluorodeoxyglucose-positron emission tomography/computed tomography, also, showed a solitary hepatic lesion in the right hepatic lobe with the mean standardized uptake value of 2.54

Figure 4 ⁶⁸Ga-prostate-specific membrane antigen positron emission tomography/computed tomography was performed for a 53-year-old male with high-grade transitional cell carcinoma of the ureter received chemotherapy. The patient presented with abdominal pain, bowel obstruction, and colostomy bag. The scan revealed prostate-specific membrane antigen uptake in peritoneal implants

Figure 5 ^99mTc-prostate-specific membrane antigen whole-body scintigraphy was performed for a 42-year-old woman with a history of cholangiocarcinoma. The scan revealed a prostate-specific membrane antigen avid hepatic lesions

Figure 6 A 5-year-old male with a history of pancreatoblastoma underwent ⁶⁸Ga-prostate-specific membrane antigen positron emission tomography/ computed tomography. There are large multiple and lobulated hypodense masses with high prostate-specific membrane antigen uptake throughout the right liver lobe suggested metastatic lesions (maximum standardized uptake value = 7.99) (a). Furthermore, there are soft-tissue lesions in the left side of the abdomen (lateral wall of the abdomen adjacent to the abdominal wall below the left kidney (2.77 cm × 2 cm with maximum standardized uptake value = 3.89 and 2.7 cm × 2.04 cm with maximum standardized uptake value = 3.04) (b) and the pancreatic head (2 cm with maximum standardized uptake value = 5.21) (c). The fluorodeoxyglucose positron emission tomography/computed tomography revealed only the hepatic lesions (maximum standardized uptake value = 6.6) and the lesion between the stomach fundus and spleen (maximum standardized uptake value = 2.8)

Figure 7 ⁶⁸Ga-prostate-specific membrane antigen positron-emission tomography/computed tomography was performed for an 8-year-old male with a history of hepatoblastoma. The scan revealed mild radiotracer uptake in the liver

Figure 8 ^99mTc-prostate-specific membrane antigen whole-body scintigraphy was performed for a 44-year-old male with unknown origin cancer revealed multifocal uptake more pronounced pelvis. The prostate cancer origin excluded according to the prostate magnetic resonance imaging, serum prostate-specific antigen level (0.83 ng/ml) and immunohistochemistry report. The whole-body bone scan, magnetic resonance imaging and fluorodeoxyglucose-positron-emission tomography showed multiple osseous metastasis in the thoracic and lumbar spine, some ribs, bilateral pelvic bones, and both femurs

Conclusion

Regarding the current literature, interpretation and reporting the PSMA scan in prostate cancer needs careful evaluation as its specificity is limited by some false-positive findings. These limitations may increase the diagnostic pitfalls and decrease the confidence of interpreting physicians. Nonspecific uptakes of ⁶⁸Ga - labeled PSMA PET/CT and ^99mTc/177Lu-PSMA scintigraphy for prostate imaging at the other malignancies apart from prostate cancer are being reported. Case reports have shown PSMA avidity in high-grade gliomas, lung cancer, breast cancer, multiple myeloma, and malignant melanoma due to the PSMA expression in the endothelial cells of the tumor neovasculature. The finding of PSMA expression in these malignancies may lead to radioligand-based therapeutic options.

Declaration of patient consent

The authors certify that they have obtained all appropriate patient consent forms. In the form the patients have given their consent for their images and other clinical information to be reported in the journal. The patients understand that their names and initials will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed.

Conflict of Interest

There are no conflicts of interest.

Financial support and sponsorship

Nil.

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Publikationsverlauf

Eingereicht: 28. Oktober 2019

Angenommen: 28. Dezember 2019

Artikel online veröffentlicht:
19. April 2022