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Clinical Trial
. 2010 Jun 1;77(2):509-15.
doi: 10.1016/j.ijrobp.2009.04.070. Epub 2009 Aug 21.

Accelerated partial breast irradiation with IMRT: new technical approach and interim analysis of acute toxicity in a phase III randomized clinical trial

Lorenzo Livi  1 , Fabrizio Banci Buonamici, Gabriele Simontacchi, Vieri Scotti, Massimiliano Fambrini, Antonella Compagnucci, Fabiola Paiar, Silvia Scoccianti, Stefania Pallotta, Beatrice Detti, Benedetta Agresti, Cinzia Talamonti, Monica Mangoni, Simonetta Bianchi, Luigi Cataliotti, Livia Marrazzo, Marta Bucciolini, Giampaolo Biti
Affiliations
Clinical Trial

Accelerated partial breast irradiation with IMRT: new technical approach and interim analysis of acute toxicity in a phase III randomized clinical trial

Lorenzo Livi et al. Int J Radiat Oncol Biol Phys. .

Abstract

Purpose: To evaluate with a randomized clinical trial the possibility of treating the index quadrant with external intensity-modulated radiotherapy (IMRT) in a selected group of patients with early-stage breast cancer and to analyze the acute toxicity.

Methods and materials: From September 2005, a randomized Phase III clinical trial has been conducted to compare conventional (tangential field) fractionated whole breast treatment (Arm A) with accelerated partial breast irradiation plus intensity-modulated radiotherapy (Arm B). For intensity-modulated radiotherapy, the clinical target volume was drawn with a uniform 1-cm margin around the surgical clips in three dimensions. The ipsilateral and contralateral breast, ipsilateral and contralateral lung, heart, and spinal cord were contoured as organs at risk. All the regions of interest were contoured according to the International Commission on Radiation Units and Measurements reports 50 and 62 recommendations.

Results: In September 2008, 259 patients were randomized and treated. The mean clinical target volume in Arm B was 44 cm(3) and the mean planning target volume was 123 cm(3). The mean value of the ratio between the planning target volume and the ipsilateral breast volume was 21%. The rate of Grade 1 and Grade 2 acute skin toxicity was 22% and 19% in Arm A (Radiation Therapy Oncology Group scale), respectively. The tolerance in Arm B was excellent with only 5% Grade 1 and 0.8% Grade 2 acute skin toxicity. The planning constraints were fully satisfied in most patients. In a very few cases, this was not possible because of very unfavorable anatomy. Quality assurance procedures were performed according to our internal quality assurance protocol, with excellent results.

Conclusion: In the present preliminary analysis, we have demonstrated that accelerated partial breast irradiation is feasible, with very low acute toxicity.

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