Interstitial brachytherapy achieved 94% local control in complex non-melanoma skin cancer

Definitive interstitial or hybrid brachytherapy controlled 94% of difficult BCC/SCC lesions, although 8% developed grade 3–4 late toxicity.

KEY POINTS

  • This single-centre retrospective study included 49 patients with 50 lesions unsuitable for conventional superficial treatment. Median age was 78.6 years; 37 lesions were BCC and 13 SCC, while 22/50 were recurrent after prior surgery.
  • Disease was often anatomically challenging: 44% of lesions were T3, and the most common locations were the periorbital region (42%) and external nose (22%).
  • Pure interstitial brachytherapy was used in 35 lesions (70%), while 15 (30%) received a hybrid interstitial plus surface-applicator approach. HDR was used in 30 lesions and PDR in 20.
  • HDR schedules delivered 40–45 Gy in 8–13 twice-daily fractions. PDR delivered 42.5–60 Gy using hourly 0.5–0.6-Gy pulses over 4–5 days. Median CTV V100 was 96.5%.
  • At a median follow-up of 21.2 months, crude local control was 94%, with only three local failures; estimated 2-year local control was 93.6%. Control was similar for BCC versus SCC (94.6% vs 92.3%) and PDR versus HDR (95.0% vs 93.3%).
  • Early tissue reactions were substantial: 26.5% had grade 3 and 14.3% grade 4 acute reactions, mainly prolonged healing or tumor-bed necrosis. The authors caution that early necrosis after definitive treatment of infiltrative skin cancers may not behave like conventional toxicity scoring.
  • Late grade 3 toxicity occurred in 2% and grade 4 in 6%, with grade 4 events representing chronic ulceration requiring wound care. Higher T stage was the only significant predictor of grade ≥2 late toxicity (p=0.044); HDR versus PDR was not (p=0.28).

CLINICAL TAKEAWAY

Interstitial or hybrid brachytherapy can provide high local control when superficial RT or surgery is poorly suited to deep, recurrent or anatomically difficult NMSC. The trade-off is meaningful tissue toxicity in more advanced lesions, and the study is not large enough to establish equivalence between HDR and PDR approaches.

SOURCE

Clinical and Translational Radiation Oncology

Browse more research Suggest a correction