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The importance of 177Lu-PSMA in the treatment of castration-resistant prostate cancer


Authors: Y. Benderli Cihan
Authors‘ workplace: Department of Radiation Oncology, Kayseri City Hospital, Kayseri, Turkey
Published in: Klin Onkol 2021; 34(2): 151-152
Category:
doi: https://doi.org/10.48095/ccko2021151

The importance of 177Lu-PSMA in the treatment of castration-resistant prostate cancer

There are some treatment options for metastatic and castration-resistant prostate cancer, and there is no single standardized treatment protocol today. In this group of patients, the chance of success in the treatment increased with the introduction of abiraterone, enzyalutamide/apalutamide, taxane chemo­therapy (docetaxel, cabazitaxel) and immunotherapy (ipilimumab, sunitinib, cabozantinib, or xofigo). Although there was an increase in both disease-free and overall survival, resistance to these drugs developed within 1-2 years. Therefore, the search for new treatments has continued [1–3]. In recent years, 223radium and 177lutetium (177Lu) prostate-specific membrane antigen (PSMA) have been shown to provide effective treatment of metastatic and castration-resistant prostate cancer with the application of radiopharmaceuticals containing ionizing radiation. The use of 177Lu-PSMA treatment, which is a radionuclide treatment, is increasing day by day [4–6].

PSMA is a transmembrane glycoprotein with enzyme functions in the cell. It takes part in cell migration, cell survival and proliferation. Although healthy prostate epithelial cells have low expression, prostate cancer can be found in rates up to 1,000-times. This has made the PSMA molecule a target for radiopharmaceuticals in the dia­gnosis and treatment of prostate cancer. First of all, radiopharmaceuticals using antibody-mediated carrier molecules have been developed and used limitedly for imaging and treatment purposes. Later, small molecular weight molecules developed from inhibitors of the enzyme component of the molecule were marked with radionuclides such as 68Ga, 18F, 44Sc, 177Lu, 225Ac, 211At and many treatment and imaging radiopharmaceuticals developed in this way quickly entered clinical use and became widespread. 177Lu was the most preferred among these. It is a radionuclide with a half-life of 6.64 days and emits beta and gamma rays. While beta rays from 177Lu decay are used to kill tumor cells, gamma rays are used for patient imaging and dosimetry studies [1–3,7–8].

It is administered intravenously to the patient in the form of 177Lu-PSMA-617 or 177Lu-PSMA I&T radiopharmaceutical. This radiopharmaceutical is collected intensely in the structure and the tumor is treated through the beta rays emitted. Standard activity after the application is 3–8 GBq. This treatment is repeated 4- or 6-times with an average interval of 2 months. With the internal dosimetry calculations to be made before or after the treatment, it is possible to select patients with higher doses or those who may develop toxicity in fixed dose protocols, albeit few [3,4,8,9]. Due to the distribution of radiation within the body; critical organs sensitive to radiation such as kidney, bone marrow and liver take the same dose. These critical organ doses are one of the most important factors affecting the number of treatments. To monitor these side effects, complete blood count, serum creatinine level, alanine aminotransferase, aspartate aminotransferase levels are measured before and after the application of 177Lu-PSMA treatment. Treatment response evaluation is basically performed by monitoring serum alkaline phosphatase, serum prostate specific antigen (PSA) level and PSMA positron emission tomographic (PET) imaging. Although it is generally accepted that PSA level and PSMA PET should be performed after at least two cycles of treatment, there is no consensus about when to evaluate the treatment [1–4].

It has not been approved by the U.S. Food and Drug Administration or the European Medicines Agency for the treatment of 177Lu-PSMA and therefore no formal criteria for patient involvement have been defined. The therapy is currently carried out under retrospective evidence, expert opinion or under local regulations for unproven interventions for patients who have exhausted all treatment options. 177Lu-PSMA treatment is preferred if it is refractory to standard antineoplastic treatments or second-generation antiandrogen treatments or if these treatments cannot be applied and if there is more than 5 meta­static lesions in the 68Ga-PET PSMA imaging. The use of 177Lu-PSMA therapy is based on the last 10 years, and its first use has started in cases where there is no other treatment option [10–13]. With this treatment, bio­chemical response (more than 50% reduction in PSA) occurred in approximately 43–66% of patients [2–5].It has been shown to have positive effects on both total survival and disease-free survival, as well as providing severe pain palliation [1,2,4]. In a phase II study in which 30 patients were included, the rate of the decrease in PSA levels by > 50% was found to be 57%. In the same study, the progression-free survival was found to be 7.6 months and the median survival was 13.5 months [10]. In another published study, it was reported that 177Lu-PSMA-617 treatment only reduced PSA, compared to salvage radiotherapy and treatment with abiraterone in lymph node metastatic prostate cancer [6]. In the study conducted by Yadav et al to determine the palliative effect of 177Lu-PSMA treatment in patients with castration-resistant prostate cancer, it was stated that pain and overall quality of life scores were significantly improved with 177Lu-PSMA [7]. In a phase I–II study conducted by Tagawa et al, it was stated that the application of 177 Lu-J591 to the fraction in the metastatic castration resistant prostate cancer marked a higher dose administration. Accordingly, it has been reported that overall survival, toxicity, and response to PSA increased at higher doses [8]. In another study, it was stated that hyperfractionated regimens were not superior to fractional application [11].

Meta-analyzes started to be carried out upon the positive reporting of the retrospective study results. Von Eyben et al revealed a meta-analysis of systemic treatment options (such as docetaxel, cabazitaxel, abiraterone and enzalutamide), which are known to prolong survival, and 12 retrospective case series undergoing the treatment with 177Lu-PSMA. In 43% of patients who received 177Lu-PSMA, the maximum PSA reduction after the treatment was ≥ 50%, while the PSA decrease following third line therapy was observed in 21% of patients. It has been reported that it provides better PSA reduction if there are fewer side effects, and it is also the first and only study showing the contribution of 177Lu-PSMA to survival [5].

In another systemic examination and meta-analysis, it has been reported that 177Lu-PSMA is effective and reliable in me­tastatic castration resistant prostate cancer [7]. In the meta-analysis performed by Kim et al, the first cycle of 177Lu-PSMA-617 radioligand therapy was reported. He stated that after two cycles, two thirds of the patients had a PSA decrease and more than 50% of the PSA reduction was expected. He noted that prolonged survival was observed due to a decrease in PSA [12].

When the literature is examined, published studies are retrospective. There are currently no prospective randomized studies published. Nowadays, a phase III study (VISION Trial) targeting 750 case participation is ongoing. As a result of this study, treatment responses and side effects of 177Lu-PSMA treatment (in which patient groups, when, and at what dosages) will become clearer [13].

As a result, 177Lu-PSMA is one of the new and promising teranostic treatment options in the treatment of metastatic castration resistant prostate cancer. Despite data on its application, efficacy and clinical reliability covering nearly 10 years, there are no phase III studies that have been completed yet. For this reason, it is partly accepted as a treatment method for research purposes and it is applied in accordance with national legislation, taking into account ethical rules. Prospective randomized studies are strongly needed to verify the effectiveness of 177Lu-PSMA with randomized control studies, to investigate its contribution to survival, earlier administration and combinations with other treatments.

The authors declare they have no potential confl icts of interest concerning drugs, products, or services used in the study.

Autoři deklarují, že v souvislosti s předmětem studie nemají žádné komerční zájmy.

The Editorial Board declares that the manuscript met the ICMJE recommendation for biomedical papers.

Redakční rada potvrzuje, že rukopis práce splnil ICMJE kritéria pro publikace zasílané do biomedicínských časopisů.

Yasemin Benderli Cihan, MD

Department of Radiation Oncology,

Kayseri City Hospital

Şeker District, Muhsinyazıcıoğlu

Boulevard, No:77

38080 Kocasinan/Kayseri

Turkey

e-mail: cihany@erciyes.edu.tr

Submitted/Obdrženo: 18. 7. 2020

Accepted/Přijato: 15. 9. 2020


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