Cosmetic Results and Side Effects of Accelerated Partial-Breast Irradiation Versus Whole-Breast Irradiation for Low-Risk Invasive Carcinoma of the Breast: The Randomized Phase III IRMA Trial

Author:

Meduri Bruno1ORCID,Baldissera Antonella2,Iotti Cinzia3ORCID,Scheijmans Luc J.E.E.4ORCID,Stam Marcel R.5,Parisi Salvatore6,Boersma Liesbeth J.7,Ammendolia Ilario8ORCID,Koiter Eveline9,Valli Mariacarla10,Scandolaro Luciano11,Busz Dianne12ORCID,Stenfert Kroese Marika C.13,Ciabatti Selena2,Giacobazzi Patrizia1,Ruggieri Maria P.3,Engelen Antoine4,Munafò Tindara6,Westenberg A. Helen5ORCID,Verhoeven Karolien7,Vicini Roberto14ORCID,D'Amico Roberto1415,Lohr Frank1,Bertoni Filippo1,Poortmans Philip1617ORCID,Frezza Giovanni P.2

Affiliation:

1. Department of Radiation Oncology, University Hospital of Modena, Modena, Italy

2. Department of Radiation Oncology, Bellaria Hospital—AUSL Bologna, Bologna, Italy

3. Department of Radiation Oncology, Azienda USL-IRCCS di Reggio Emilia, Reggio Emilia, Italy

4. Department of Radiation Oncology, Instituut Verbeeten, Tilburg, the Netherlands

5. Radiotherapiegroep, Arnhem/Ede, the Netherlands

6. Department of Radiation Oncology, Casa Sollievo della Sofferenza, San Giovanni Rotondo, Italy

7. Department of Radiation Oncology (Maastro), Maastricht University Medical Centre+—GROW School for Oncology and Reproduction, Maastricht, the Netherlands

8. Department of Radiation Oncology, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy

9. Department of Radiation Oncology, Medisch Spectrum Twente, Enschede, the Netherlands

10. Department of Radiation Oncology, IOSI (Oncology Institute of Italian Switzerland), Bellinzona, Switzerland

11. Department of Radiation Oncology, Presidio Ospedaliero S.Anna—ASST Lariana, San Fermo della Battaglia—Como, Italy

12. Department of Radiation Oncology, University of Groningen—University Medical Center Groningen, Groningen, the Netherlands

13. Radiotherapiegroep, Deventer/Apeldoorn, the Netherlands

14. Department of Methodological and Statistical Support for Clinical Research, University Hospital of Modena, Modena, Italy

15. Department of Medical and Surgical Sciences, University of Modena and Reggio Emilia, Modena, Italy

16. Department of Radiation Oncology, Iridium Netwerk, Wilrijk-Antwerp, Belgium

17. Faculty of Medicine and Health Sciences, University of Antwerp, Wilrijk-Antwerp, Belgium

Abstract

PURPOSE The results in terms of side effects vary among the published accelerated partial-breast irradiation (APBI) studies. Here, we report the 5-year results for cosmetic outcomes and toxicity of the IRMA trial. METHODS We ran this randomized phase III trial in 35 centers. Women with stage I-IIA breast cancer treated with breast-conserving surgery, age ≥ 49 years, were randomly assigned 1:1 to receive either whole-breast irradiation (WBI) or external beam radiation therapy APBI (38.5 Gy/10 fraction twice daily). Patients and investigators were not masked to treatment allocation. The primary end point was ipsilateral breast tumor recurrence. We hereby present the analysis of the secondary outcomes, cosmesis, and normal tissue toxicity. All side effects were graded with the Radiation Therapy Oncology Group/European Organisation for Research and Treatment of Cancer Radiation Morbidity Scoring Schema. Analysis was performed with both intention-to-treat and as-treated approaches. RESULTS Between March 2007 and March 2019, 3,309 patients were randomly assigned to 1,657 WBI and 1,652 APBI; 3,225 patients comprised the intention-to-treat population (1,623 WBI and 1,602 APBI). At a median follow-up of 5.6 (interquartile range, 4.0-8.4) years, adverse cosmesis in the APBI patients was higher than that in the WBI patients at 3 years (12.7% v 9.2%; P = .009) and at 5 years (14% v 9.8%; P = .012). Late soft tissue toxicity (grade ≥ 3: 2.8% APBI v 1% WBI, P < .0001) and late bone toxicity (grade ≥ 3: 1.1% APBI v 0% WBI, P < .0001) were significantly higher in the APBI arm. There were no significant differences in late skin and lung toxicities. CONCLUSION External beam radiation therapy-APBI with a twice-daily IRMA schedule was associated with increased rates of late moderate soft tissue and bone toxicities, with a slight decrease in patient-reported cosmetic outcomes at 5 years when compared with WBI, although overall toxicity was in an acceptable range.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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