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Systemic therapy escalation after stereotactic body radiation therapy for oligometastatic hormone-sensitive prostate cancer. | LitMetric

AI Article Synopsis

  • The study aimed to assess the outcomes of stereotactic body radiation therapy (SBRT) in patients with oligometastatic hormone-sensitive prostate cancer (omHSPC), focusing on systemic therapy escalation-free survival (STE-FS) and other relapse types.
  • Out of 119 patients treated with SBRT, the median STE-FS was 33.4 months, with a local control rate of 95%, though progression events occurred in 60.5% of the patients.
  • The findings suggest that SBRT offers good local control with minimal severe side effects, making it a promising option for delaying the start of more intense systemic treatments, but more research is needed for better patient selection and longer-term

Article Abstract

Purpose: To evaluate the oncological outcome after stereotactic body radiation therapy (SBRT) for oligometastatic hormone-sensitive prostate cancer (omHSPC) patients.

Materials-methods: In this retrospective, observational, multi-institutional study, omHSPC patients (≤5 metastases) underwent SBRT. Primary endpoint was systemic therapy escalation-free survival (STE-FS) after SBRT. Local (LR), distant (DR), prostatic (PR) and isolated biochemical (iBR) relapses were reported with progression-free survival (PFS) and overall survival (OS). Prognostic factors for STE-FS were investigated. Toxicity was reported.

Results: From 01/07 to 09/19, 119 pts with omHSPC underwent SBRT. With a MFU of 34 months [12-97], median STE-FS was 33.4 months (95%CI 26.6---40.1). Median OS was not reached and PFS was 22.7 months (CI95% 18.6---32.3). Post-SBRT-PSA remained stable or decreased in 87 pts (73.1%). Progression events (LR, MR, PR, iBR) were observed in 72 pts (60.5%), among whom 6 relapsed in the irradiated area (local control rate: 95%). DR, BR, PR were observed in 44 pts (37%), 21pts (17.7%) and 2 pts (1.7%) respectively. In multivariate analysis, post-SBRT biochemical response was an independent prognostic factor for STE-FS. Grade ≥ 3 toxicity occurred in 1pt.

Conclusion: With excellent local control and tolerance, SBRT for omHSPC patients represents an attractive approach to defer systemic therapeutic escalation and prevent its side effects. Accurate patient selection for SBRT requires more data with longer follow-up and higher numbers of patients pending the results of upcoming randomized trials.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10493250PMC
http://dx.doi.org/10.1016/j.ctro.2023.100673DOI Listing

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