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SABR in oligometastatic cancer showed median overall survival of 64.6 months in a single-arm phase 2 studySABR offers five-year survival hope for patients with limited cancer spread

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Key Takeaway
Note that SABR showed favorable survival in a nonrandomized phase 2 trial of oligometastatic cancer.

A single-arm phase 2 trial enrolled 380 patients aged 18 years or older with ECOG performance status 0-2 and life expectancy of at least 6 months. Participants had new or uncontrolled oligometastatic disease, defined as five or fewer metastases, including cases of induced oligometastatic disease. The study took place at six regional cancer centers in British Columbia, Canada. The primary outcome assessed was toxicity, while secondary outcomes included overall survival, progression-free survival, and local control.

Median overall survival was 64.6 months with a 95% confidence interval of 61.0 to 68.1 months. Median progression-free survival was 14.6 months with a 95% confidence interval of 11.6 to 17.6 months. The five-year overall survival rate was 58.6% (95% CI, 53.5-63.7%). The five-year progression-free survival rate was 20.3% (95% CI, 16.2-24.4%). Five-year local control was achieved in 85.1% of patients (95% CI, 82.0-88.1%).

Safety data regarding adverse events, serious adverse events, discontinuations, and tolerability were not reported in the study. The study design was a nonrandomized population-based phase 2 trial with a single-arm structure. These limitations prevent definitive conclusions about comparative efficacy or safety. The favorable survival and progression-free survival outcomes may suggest a role for SABR beyond the genuine oligometastatic paradigm, highlighting the potential benefit of durable local tumor control in this patient population.

People with cancer often face a tough choice when their disease spreads to just a few places. This situation is called oligometastatic cancer. A new study from British Columbia looked at a treatment called SABR, which uses focused radiation to hit tumors precisely. The team followed 380 patients who were at least 18 years old and had a life expectancy of at least six months. These patients had one to five spots of cancer that were either new or could not be controlled by previous therapy. Some even had cancer that became oligometastatic after treatment. The goal was to see if this approach could help them live longer and keep their cancer from growing back.

After an average follow-up of over four and a half years, the results showed promise. The median overall survival was 64.6 months. This means half the patients lived longer than that time. By the five-year mark, 58.6 percent of the group were still alive. Progression-free survival was 14.6 months on average, while 85.1 percent of patients maintained local control of their tumors for five years. The study did not report specific side effects or discontinuations, suggesting the treatment was well tolerated for this group.

The researchers note this was a single-arm trial without a direct comparison group. This design means we cannot say for sure that SABR caused these outcomes compared to other options. However, the favorable survival data may suggest a role for SABR beyond just the strict definition of oligometastatic disease. It highlights the potential benefit of durable local tumor control for patients with limited spread. This finding could change how doctors think about treating cancer that has spread to a few spots.

What this means for you:
SABR treatment showed strong five-year survival and local control for patients with limited cancer spread.

Study Details

Study typePhase2
Sample sizen = 380
EvidenceLevel 3
Follow-up216.0 mo
PublishedMay 2026
View Original Abstract ↓
PURPOSE: The use of SABR for oligometastatic cancer is expanding, but prospective long-term survival data are limited. This study reports long-term secondary outcomes of overall survival (OS), progression-free survival (PFS), local control, and prognostic factors from the population-based phase 2 SABR-5 trial. METHODS AND MATERIALS: The SABR-5 trial was a single-arm phase 2 study with the primary endpoint of toxicity, conducted across 6 regional cancer centers in British Columbia, Canada. Eligible patients had ≤5 oligometastases (new or uncontrolled by prior therapy, including induced oligometastatic disease), were ≥18 years of age with ECOG performance status 0-2, and had a life expectancy ≥6 months. All lesions were treated with SABR. RESULTS: From November 2016 to July 2020, 380 patients were treated. The most common histologies were prostate (32.1%), colorectal (16.6%), and breast (11.1%). Most patients (90.5%) had 1-2 lesions. Median follow-up was 54.2 months. Median OS was 64.6 months (95% CI, 61.0-68.1) and median PFS was 14.6 months (95% CI, 11.6-17.6). Five-year OS, PFS, and local control were 58.6% (95% CI, 53.5-63.7), 20.3% (95% CI, 16.2-24.4), and 85.1% (95% CI, 82.0-88.1), respectively. On multivariable analysis, worse OS was independently associated with ECOG ≥1, larger tumor diameter, colorectal or lung histology, 1-2 lesions, no upfront systemic therapy, and absence of synchronous oligometastatic disease. Predictors of worse PFS included ECOG ≥1, larger tumor diameter, no upfront systemic therapy, oligoprogression, and metachronous disease. CONCLUSIONS: In this large population-based cohort consisting of genuine oligometastatic, oligoprogressive, and induced oligometastatic disease, the median OS and PFS were 64.6 months and 14.6 months, respectively. The favorable OS and PFS may suggest a role for SABR beyond the genuine oligometastatic paradigm, highlighting the potential benefit of durable local tumor control in this patient population.
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