Epidemiology and natural history of non-metastatic castration-resistant prostate cancer in Russia

Author:

Alekseev B. Ya.1ORCID,Nyushko K. M.1ORCID,Gafanov R. A.2ORCID,Kirichek A. A.3ORCID,Anzhiganova Yu. V.4ORCID,Kopyltsov E. I.5ORCID,Sundui Yu. Yu.6ORCID,Pashanov Е. D.7ORCID,Petyushin A. N.7ORCID,Matveev V. B.8ORCID

Affiliation:

1. National Medical Research Radiological Center, Ministry of Health of Russia; Medical Institute of Continuing Education, Moscow State University of Food Production

2. Russian Scientific Center of Roentgen Radiology, Ministry of Health of Russia

3. Moscow City Oncological Hospital No. 62, Moscow Healthcare Department

4. A.I. Kryzhanovsky Krasnoyarsk Regional Clinical Oncology Dispensary

5. Omsk Clinical Oncology Dispensary

6. City Clinical Cancer Hospital No. 1, Moscow Healthcare Department

7. Johnson & Johnson, pharmaceutical companies

8. N.N. Blokhin National Medical Research Center of Oncology, Ministry of Health of Russia

Abstract

Aim. To study the clinical and demographic profile of patients with non-metatstatic castration-resistant prostate cancer (nmCRPC) and clinical approaches to the treatment of nmCRPC in the context of daily medical practice before and after progression M1 stage.Materials and methods. The multicenter non-interventional epidemiological study were included 200 patients with a documented diagnosis of nmCRPC from 2019 to 2020. Each patient visited twice: start and after 6 months. Of the 200 patients included, 9 were excluded from the analysis presented in this article: 1 patient had no information on inclusi- on criteria, 1 patient did not meet the inclusion criteria, 7 patients did not attend visit 2. Thus, data are presented for 191 patients.Results and conclusion. The median age was 74.3 years (range 55 to 91). 72 % (137/191) had a disability group. The most common comorbidities were hypertension (n = 115) and hypercholesterolemia (n = 56). The median time from the diagnosis of prostate cancer to the development of castration resistance (diagnosis of nmCRPC) was 75 months. Prostate specific antigen (PSA) nadir (0.37 ng/ml on average) was achieved after 15 months of prostate cancer therapy (median time to reach PSA nadir). At the same time, PSA doubling time in most cases (47.6 %; 91/191) was less than 6 months, 18.8 % of persons (36/191) had PSA doubling time for more than 10 months.

Publisher

Publishing House ABV Press

Subject

Urology,Nephrology,Radiology, Nuclear Medicine and imaging,Oncology,Surgery

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