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SMART radiation shows 90% 4-year local control in small oligometastatic abdominopelvic cohort

SMART radiation shows 90% 4-year local control in small oligometastatic abdominopelvic cohort
Photo by Brett Jordan / Unsplash
Key Takeaway
Consider SMART's high local control in oligometastases as preliminary data from a small, single-arm trial.

This was a single-arm prospective Phase 1/2 clinical trial evaluating the feasibility and safety of Stereotactic Magnetic Resonance-Guided Adaptive Radiation Therapy (SMART) for treating metachronous oligometastases. The study enrolled 10 patients with solid tumors (8 prostate, 2 renal cell carcinoma) who had 3 or fewer abdominopelvic nodal or soft tissue metastases, each measuring 7 cm or less. All patients received SMART to a dose of 40 Gy delivered in 5 fractions.

With a median follow-up of 4.22 years, the main outcomes were 90% 4-year local control and 90% 4-year overall survival. The 4-year distant progression-free survival rate was notably lower at 20%. Regarding safety, the treatment was well-tolerated; all 10 patients completed the protocol without complications, and only 3 patients experienced acute grade 1 toxicities, with no higher-grade or late toxicities reported.

Key limitations include the very small sample size (n=10), the absence of a comparator group, and the single-arm design, which precludes establishing causality or comparative efficacy. The long-term efficacy and safety beyond the reported 4-year follow-up are not described. The study population was also specific, consisting only of patients with prostate or renal cell carcinoma metastases.

In practice, these findings represent preliminary evidence from an early-phase feasibility study. The high local control and favorable toxicity profile are encouraging for this precise radiation technique in a select oligometastatic population. However, clinicians should interpret these results with caution due to the significant limitations and await confirmatory data from larger, controlled trials before drawing definitive conclusions about the role of SMART in this setting.

Study Details

Study typePhase1
Sample sizen = 10
EvidenceLevel 4
Follow-up12.0 mo
PublishedApr 2026
View Original Abstract ↓
PURPOSE: Metachronous oligometastases may represent a favorable disease state for local therapy after prior curative treatment. Stereotactic Magnetic Resonance-Guided Adaptive Radiation Therapy (SMART) provides precise targeting of nodal and soft tissue metastases. The primary objective was to assess the feasibility and safety of SMART for abdominopelvic metachronous oligometastases. Secondary objectives included assessing rates of toxicities and evaluating local control (LC). METHODS AND MATERIALS: Ten patients were enrolled with solid tumor metachronous abdominopelvic nodal or soft tissue metastases, ≤7 cm in maximal diameter, and ≤3 sites of active disease. All patients received 40 Gy in 5 fractions. Acute toxicities were graded per Common Terminology Criteria for Adverse Events v5 per-protocol follow-up over 1 year. Late toxicities and clinical outcomes were elucidated by chart review. LC, distant progression-free survival, and overall survival were analyzed using the Kaplan-Meier Method. RESULTS: Eight patients with prostate cancer and 2 with renal cell carcinoma were enrolled in the study. All patients were successfully treated with SMART per-protocol without complications. The median follow-up after SMART was 4.22 years. Three patients experienced acute grade 1 toxicities; there were no higher grade or late toxicities. Among these 10 patients, 4-year LC and overall survival were both 90%, and 4-year distant progression-free survival was 20%. Two patients (1 prostate cancer, 1 renal cell carcinoma) remain with no evidence of disease, each at over 4 years following SMART and without receiving further systemic or local therapies. CONCLUSIONS: With 4 years median follow-up, this small prospective trial reports low toxicity, supporting the feasibility of SMART metastasis-directed therapy for metachronous oligometastases with minimal risk of acute or late toxicity.
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