Hypofractionated HDR plesiotherapy in nonmelanoma skin cancer
ForClinically N0 BCC/SCC skin, primary or recurrent, definitive or adjuvant
TL;DR3y/5y DFS 95.12%/93.36% after 3 Gy/fx HDR surface brachy for 134 BCC/SCC lesions; CR 98%, recurrent lesions did worse.
Disease status, not applicator, split control: recurrent lesions reached 3y/5y DFS 85.9%/85.9% vs 97.9%/95.6% for primary (p=0.003). Acute G3 was 40.3% at 3 Gy/fx three times weekly, higher with definitive intent and molds, so fraction size and applicator choice gate tolerability more than control for larger or curved lesions.
In older pts with a small flat primary BCC or SCC, this supports HDR surface brachy at 3 Gy/fx as a definitive option with high control; it is weaker support for recurrent lesions, where 5y DFS was 85.9%.
Disease status, not applicator, split control: recurrent lesions reached 5y DFS 85.9% vs 95.6% for primary (p=0.003). Acute G3 was 40.3% at 3 Gy/fx three times weekly, higher with definitive intent and molds, so fraction size and applicator choice gate tolerability for larger or curved lesions.
13 details
Retrospective single-institution series, 114 pts and 134 lesions treated Nov 2006 to Dec 2011. Analysis per lesion; median follow-up 33 mo.
92 BCC and 42 SCC, all clinically N0. 77.3% definitive, 22.7% adjuvant after excision with positive or close margins.
Ir-192 HDR plesiotherapy, 3 Gy/fx, 3 fx/wk; mean 48.79 Gy (45-54) for BCC and 50.55 Gy (45-57) for SCC, prescribed 3-5 mm below the surface with a 0.5-1 cm margin. Leipzig 2 or 3 cm applicators for flat lesions ≤2 cm (75.4%); customized molds for raised or larger lesions.
Overall 3y/5y DFS 95.12%/93.36%, CR 98%. Recurrent lesions did worse than primary (85.9% vs 95.6% at 5y, p=0.003); applicator and definitive vs adjuvant did not separate DFS.
| Group | 3y DFS | 5y DFS |
|---|---|---|
| Overall | 95.12% | 93.36% |
| Leipzig applicator | 94.9% | 94.9% |
| Customized mold | 93.1% | 88% |
| Primary lesion | 97.9% | 95.6% |
| Recurrent lesion | 85.9% | 85.9% |
| BCC | 94.1% | 91.3% |
| SCC | 97.5% | 97.5% |
Acute RTOG G3 40.3%, G4 2.2%; toxicity higher with definitive intent (OR 2.928, p=0.013) and borderline with molds (p=0.067). Late G0-1 95.2%; cosmesis excellent/good 82%.
Authors place results alongside the Kohler Leipzig series (91% complete remission) and Guix's mold series (5y DFS 98%). They cite one randomized surgery vs RT trial as the only head-to-head data, with no numbers given in source.
Molds treated larger lesions, so mold vs Leipzig DFS and toxicity differences cannot be separated from size. Reported recurrence counts do not add up, and the acute toxicity figure differs between abstract and results.
Supports surface HDR as a definitive alternative to excision for small primary NMSC. It does not settle optimal fraction size, and the high acute G3 rate argues for weighing applicator and dose per fraction for larger lesions.
Retrospective single-institution series, no comparator arm; applicator comparison confounded by lesion size and location; DFS per lesion with 33-mo median f/u.
- Optimal fraction size for HDR surface brachy in NMSC
- Late recurrence and cosmesis beyond 5 years
- HDR plesiotherapy vs Mohs or excision head-to-head
📚 Sources · 📄 1 paper
The longer read
The value of this series is less the headline DFS than how it is distributed. A 5-year DFS of 93.36% across a mixed cohort of BCC and SCC, primary and recurrent, definitive and adjuvant, sits in the range most single-institution brachytherapy reports describe, and the authors place it alongside the Leipzig experience reported by Kohler and the mold technique reported by Guix. That is reassuring but not discriminating; nearly every retrospective NMSC RT series reports control in the 90s, because lesion selection does much of the work. The more useful signal is that recurrent disease separated clearly from primary (5-year DFS 85.9% vs 95.6%, p=0.003), while applicator type and definitive versus adjuvant intent did not separate meaningfully. For a radiation oncologist, that points to disease history, rather than device, as the variable worth weighing when offering surface brachytherapy as an alternative to re-excision or Mohs.
The applicator comparison is where a reader should be most cautious. Molds were used for larger lesions (mean 19.38 vs 13.07 mm) and for raised or curved surfaces, so any difference in DFS or toxicity between molds and Leipzig cones is confounded by size and anatomy. The authors attempted to address this by restricting to lesions within the Leipzig range, but the toxicity association with molds stayed borderline (p=0.067), and lesion size itself carried a significant odds ratio for acute toxicity. The 5-year DFS of 88% for molds versus 94.9% for Leipzig is better read as a size and site gradient than as evidence that one device controls disease less well. Compounding this, the paper's own accounting is not internally consistent: six recurrences are described as five Leipzig plus three mold, and the acute toxicity figure in the abstract does not match the results section. These are small errors, but in a series this size they are the kind that make subgroup p-values fragile.
The acute toxicity profile deserves more attention than the conclusion gives it. Roughly two in five lesions developed RTOG grade 3 acute reactions at 3 Gy per fraction three times weekly, and definitive treatment carried higher odds than adjuvant. Late outcomes were favourable, with grade 0-1 late toxicity in 95.2% and good or excellent cosmesis in 82%, which is the trade a surface brachytherapy patient is accepting: a brisk acute reaction that largely resolves. Follow-up of 33 months, though, is short for both late cosmesis and late BCC recurrence, so the late picture is incomplete.
What would make this wrong? If the high control reflects selection of small, favourable primaries, the result does not transfer to the recurrent or larger lesions where an RT alternative to surgery is most often requested, and the data in hand already hint that this is the case. The series supports HDR plesiotherapy as a reasonable definitive option for small primary NMSC in older pts, and gives a concrete reason to counsel recurrent-lesion pts on a lower control expectation. It does not establish a preferred fractionation, does not compare against excision or Mohs, and does not show that molds are inferior once size is accounted for.