Adjuvant hormone therapy in patients undergoing high-intensity focused ultrasound therapy for locally advanced prostate cancer
- Authors: Neimark A.I.1,2, Tachalov M.A.1,2, Neimark B.A.1,2
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Affiliations:
- Department of Urology and Nephrology, Altai State Medical University, Ministry of Health of Russia, Barnaul
- Unit of Urology and Nephrology, Departmental Clinical Hospital at the Barnaul Station, OAO “RZhD”
- Issue: Vol 10, No 3 (2014)
- Pages: 69-72
- Section: PROSTATE CANCER
- Published: 30.09.2014
- URL: https://oncourology.abvpress.ru/oncur/article/view/382
- DOI: https://doi.org/10.17650/1726-9776-2014-10-3-69-72
- ID: 382
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Abstract
Objective: to evaluate the efficiency and safety of using the luteinizing hormone releasing hormone leuprorelin with the Atrigel delivery system in doses of 7.5, 22.5, and 45 mg as an adjuvant regimen in high- and moderate-risk cancer patients who have received high-intensity focused ultrasound (HIFU) therapy.
Subjects and methods. Moderate- and high-risk locally advanced prostate cancer (PC) patients treated with HIFU (n = 28) and HIFU in combination with hormone therapy during 6 months (n = 31) were examined.
Results. The investigation has shown that leuprorelin acetate monotherapy used within 6 months after HIFU therapy can achieve the highest reduction in prostate-specific antigen levels and positively affect the symptoms of the disease. HIFU in combination with androgen deprivation substantially diminishes the clinical manifestations of the disease and improves quality of life in HIFU-treated patients with PC, by reducing the degree of infravesical obstruction (according to uroflowmetric findings and IPSS scores), and causes a decrease in prostate volume as compared to those who have undergone HIFU only. Treatment with leuprorelin having the Atrigel delivery system has demonstrated the low incidence of adverse reactions and good tolerability.
About the authors
A. I. Neimark
Department of Urology and Nephrology, Altai State Medical University, Ministry of Health of Russia, Barnaul; Unit of Urology and Nephrology, Departmental Clinical Hospital at the Barnaul Station, OAO “RZhD”Russian Federation
M. A. Tachalov
Department of Urology and Nephrology, Altai State Medical University, Ministry of Health of Russia, Barnaul; Unit of Urology and Nephrology, Departmental Clinical Hospital at the Barnaul Station, OAO “RZhD”
Author for correspondence.
Email: med7@mail.ru
Russian Federation
B. A. Neimark
Department of Urology and Nephrology, Altai State Medical University, Ministry of Health of Russia, Barnaul; Unit of Urology and Nephrology, Departmental Clinical Hospital at the Barnaul Station, OAO “RZhD”Russian Federation
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