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These studies suggest that radiation therapy, including SBRT and high-dose options, is effective for treating localized prostate cancer, with benefits in tumor control, quality of life, and low toxicity, and that combining radiation with androgen suppression or antiandrogen therapy can improve outcomes for higher-risk patients.
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Stereotactic Body Radiation Therapy (SBRT) has emerged as a promising treatment for localized prostate cancer. A systematic review and meta-analysis of over 6,000 patients treated with SBRT demonstrated high rates of biochemical recurrence-free survival (bRFS) at 5 and 7 years, with rates of 95.3% and 93.7%, respectively. The study also reported low rates of severe genitourinary (GU) and gastrointestinal (GI) toxicity, with late grade ≥3 GU and GI toxicity rates at 2.0% and 1.1%, respectively. These findings suggest that SBRT is a viable standard treatment option for localized prostate cancer, offering favorable tumor control and patient-reported quality of life.
For intermediate- and high-risk localized prostate cancer, combining radiation therapy (RT) with androgen suppression (AS) has shown significant benefits. A study involving 819 patients found that adding 6 months of AS to primary RT significantly improved biochemical disease-free survival (DFS) and clinical progression-free survival. This combination therapy reduced the hazard ratio for biochemical DFS to 0.52 and for clinical progression-free survival to 0.63, indicating a substantial improvement in patient outcomes.
Dose escalation in radiation therapy has been shown to improve cancer control in prostate cancer patients. A randomized trial comparing conventional-dose (70.2 Gy) with high-dose (79.2 Gy) conformal radiation therapy found that high-dose radiation significantly reduced local failure and biochemical failure rates. Specifically, the 10-year biochemical failure rates were 32.4% for conventional-dose and 16.7% for high-dose radiation therapy. However, despite these improvements in biochemical control, no overall survival benefit was observed.
Hypofractionated IMRT, which delivers larger daily doses of radiation over a shorter period, has also shown promise. A randomized trial comparing hypofractionated IMRT (HIMRT) with conventionally fractionated IMRT (CIMRT) found that HIMRT resulted in fewer treatment failures and a lower 8-year failure rate (10.7% vs. 15.4%). Although there was a non-significant increase in late grade 2 or 3 GI toxicity with HIMRT, the overall cancer control was superior.
For patients with recurrent prostate cancer post-prostatectomy, adding antiandrogen therapy to salvage radiation therapy has shown significant benefits. A double-blind, placebo-controlled trial demonstrated that 24 months of antiandrogen therapy with bicalutamide significantly improved overall survival and reduced the incidence of metastatic prostate cancer and death from prostate cancer compared to radiation therapy alone.
The American Urological Association (AUA) and the American Society for Radiation Oncology (ASTRO) have provided guidelines for the management of clinically localized prostate cancer, emphasizing the importance of continued research and high-quality evidence from future trials to further improve patient care. These guidelines highlight the need for personalized treatment approaches based on individual patient risk factors and the potential benefits of advanced radiation therapy techniques.
Radiation therapy for prostate cancer has seen significant advancements, with various techniques such as SBRT, dose-escalated RT, and hypofractionated IMRT showing improved cancer control and patient outcomes. Combining radiation therapy with androgen suppression or antiandrogen therapy further enhances treatment efficacy, particularly for high-risk and recurrent cases. Ongoing research and adherence to clinical guidelines will be crucial in optimizing treatment strategies and improving the quality of life for prostate cancer patients.
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