Clinical and Translational Radiation Oncology (Jan 2023)

Feasibility and early toxicity of intraoperative radiotherapy for breast cancer using the papillon + system: First results

  • Marie-Eve Chand-Fouché,
  • Claudine Colnard,
  • Jocelyn Gal,
  • Daniel Lam Cham Kee,
  • Catherine Dejean,
  • Matthieu Gautier,
  • Julien Feuillade,
  • Aurélia Mana,
  • Yves Fouché,
  • Yann Delpech,
  • Magali Dejode,
  • Jean-Pierre Gérard,
  • Emmanuel Barranger

Journal volume & issue
Vol. 38
pp. 47 – 52

Abstract

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Background and Purpose: Breast intra operative radiation therapy has been evaluated with different systems delivering 20–21 Gy with treatment times around 30 min. Papillon + TM Contact X-ray machine was designed to produce a 50 kVp beam with a high dose rate ≥ 15 Gy/minute. A pilot study with the first prototype was conducted in Nice. Materials and methods: The inclusion criteria were age ≥ 60 years, unifocal ductal breast adenocarcinoma ≤ 2.5 cm, grade 1–2. Surgical local excision with sentinel node dissection was performed and the applicator was placed in the tumor bed after excision with a prescribed dose of 20 Gy. The main end point of the study was the doses measured with the Gafchromic films; two were located at the skin surface and two in the excision cavity. Secondary endpoints were early toxicity and relapse free survival. Results: Between 10/2018 and 09/2019, 26 patients were included. Mean Gafchromic doses were 18.8 Gy ± 2 Gy at the south pole, 15.6 Gy ± 2.81 Gy at the equator and 2.5 Gy ± 1.67 Gy at the skin. With a median follow-up time of 12 months, no skin or subcutaneous toxicity > grade 2, no local relapse and no metastasis were observed. Conclusion: This is the first phase II study testing the Papillon + tm system for breast IORT with in vivo dosimetry measurements and reassuring clinical data.

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