Accelerated Partial Breast Irradiation With IMRT: New Technical Approach and Interim Analysis of Acute Toxicity in a Phase III Randomized Clinical Trial
Creators
- Livi, Lorenzo1
- Buonamici, Fabrizio Banci2
- Simontacchi, Gabriele1
- Scotti, Vieri1
- Fambrini, Massimiliano3
- Compagnucci, Antonella2
- Paiar, Fabiola1
- Scoccianti, Silvia1
- Pallotta, Stefania2
- Detti, Beatrice1
- Agresti, Benedetta1
- Talamonti, Cinzia2
- Mangoni, Monica1
- Bianchi, Simonetta4
- Cataliotti, Luigi5
- Marrazzo, Livia2
- Bucciolini, Marta2
- Biti, Giampaolo1
- 1. Radiotherapy Unit, University of Florence, Florence (Italy)
- 2. Department of Medical Physics, University of Florence, Florence (Italy)
- 3. Department of Gynaecology, Perinatology, and Human Reproduction, University of Florence, Florence (Italy)
- 4. Department of Pathology, University of Florence, Florence (Italy)
- 5. Department of Surgery, University of Florence, Florence (Italy)
Description
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 cm3 and the mean planning target volume was 123 cm3. 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.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.ijrobp.2009.04.070Additional details
Identifiers
- DOI
- 10.1016/j.ijrobp.2009.04.070;
- PII
- S0360-3016(09)00668-3;
Publishing Information
- Journal Title
- International Journal of Radiation Oncology, Biology and Physics
- Journal Volume
- 77
- Journal Issue
- 2
- Journal Page Range
- p. 509-515
- ISSN
- 0360-3016
- CODEN
- IOBPD3
INIS
- Country of Publication
- United States
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 41102755
- Subject category
- S62: RADIOLOGY AND NUCLEAR MEDICINE;
- Descriptors DEI
- CLINICAL TRIALS; FRACTIONATED IRRADIATION; MAMMARY GLANDS; NEOPLASMS; RADIOTHERAPY; TOXICITY
- Descriptors DEC
- BODY; DISEASES; GLANDS; IRRADIATION; MEDICINE; NUCLEAR MEDICINE; ORGANS; RADIOLOGY; TESTING; THERAPY
Optional Information
- Copyright
- Copyright (c) 2010 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.