SBRT did not reproduce brachytherapy dose escalation in gynecologic cancers

SBRT provided competitive peripheral coverage in some plans but could not consistently reproduce brachytherapy’s central dose escalation after realistic margins were applied.

KEY POINTS

  • The systematic review searched five databases for comparative studies published from 2014 through 2025. It included 11 studies: nine dosimetric comparisons, one population-based cohort and one consensus guideline, mainly involving locally advanced cervical cancer.
  • Brachytherapy consistently produced greater central dose escalation. In one comparison, high-risk clinical target volume D50 was 12.1 Gy per fraction with intracavitary/interstitial brachytherapy versus 9.93 Gy with SBRT; another reported cumulative D50 of 42.08 versus 32.94 Gy (p < 0.001).
  • SBRT sometimes produced higher D90, D95 or D98 and better conformity, particularly when plans were generated without a planning target volume margin. These peripheral-coverage advantages did not reproduce the 150–250% intratumoral hotspots characteristic of brachytherapy.
  • The effect of realistic margins was substantial. In a magnetic resonance-guided adaptive comparison, total high-risk clinical target volume D90 was 95.6 Gy EQD2 with margin-free SBRT but fell to 82.9 Gy after a planning target volume margin was applied, compared with 89.7 Gy using brachytherapy.
  • Organ-at-risk results were inconsistent. Some margin-free SBRT comparisons reduced bladder, rectal and sigmoid doses by 20–30%, while another found lower cumulative bladder and sigmoid doses with brachytherapy: 74.6 versus 84.7 Gy and 67.9 versus 75.75 Gy, respectively.
  • Attempting brachytherapy-like central escalation with external-beam treatment could violate organ constraints. One highly heterogeneous robotic SBRT strategy produced a bladder D2cm³ of 172.7 Gy and was judged clinically infeasible.
  • The only survival analysis included 15,905 patients, of whom 90.5% received brachytherapy and only 0.8% SBRT. Unadjusted median overall survival was 99.1 versus 30.3 months, but after propensity matching the difference was not significant (hazard ratio 1.477; 95% confidence interval, 0.746–2.926; p = 0.263).
  • Most SBRT plans were retrospective simulations rather than delivered treatments. Comparative late toxicity, patient-reported outcomes and quality-of-life data were insufficient, and the heterogeneity of schedules and planning methods prevented meta-analysis.

CLINICAL TAKEAWAY

Brachytherapy remains the reference boost technique for curative gynecologic radiotherapy because it delivers central dose escalation that external-beam SBRT cannot reliably reproduce while accounting for pelvic motion. SBRT is a fallback for patients in whom brachytherapy is genuinely impossible, not an equivalent non-invasive replacement supported by the current evidence.

SOURCE

Clinical and Translational Radiation Oncology