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Stereotactic Body Radiotherapy for Oligoprogression in Castration-Resistant Prostate Cancer: Early Toxicity Analysis
Stereotactic body radiotherapy (SBRT) for oligoprogressive disease (OPD) in metastatic castrate-resistant prostate cancer (CRPC) patients on targeted agents showed low toxicity. Quality of life remained unchanged after SBRT, with minimal SBRT-related adverse events.
Area of Science:
- Oncology
- Radiation Oncology
- Prostate Cancer Research
Background:
- Metastatic castrate-resistant prostate cancer (CRPC) patients on androgen receptor targeted agents (ARTA) can develop oligoprogressive disease (OPD).
- Stereotactic body radiotherapy (SBRT) is a potential treatment for limited metastatic sites.
Purpose of the Study:
- To evaluate the toxicity and impact on quality of life of SBRT for OPD in CRPC patients receiving ARTA.
- To assess if SBRT to OPD sites improves progression-free survival.
Main Methods:
- Phase II clinical trial enrolling CRPC patients with ≤ 2 oligoprogressive lesions on abiraterone or enzalutamide.
- Patients received SBRT (30 Gy in 5 fractions) to OPD sites while continuing ARTA.
- Toxicity assessed via Common Terminology Criteria for Adverse Events (CTCAE) and Radiation Therapy Oncology Group (RTOG) criteria; quality of life via visual analogue scale (VAS) and EQ-5D.
Main Results:
- Twenty percent (8/40) of patients experienced grade ≥ 3 toxicity, with only 2.5% (1/40) possibly related to SBRT.
- No significant difference was observed in mean EQ-5D or VAS scores from baseline to post-SBRT timepoints (p = 0.449).
Conclusions:
- SBRT for OPD in CRPC patients on ARTA is associated with low rates of severe toxicity.
- SBRT treatment did not discernibly alter patient-reported quality of life.
- Further follow-up is ongoing to report final progression-free survival and toxicity data.
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