Effect of Delayed Targeted Intraoperative Radiotherapy vs Whole-Breast Radiotherapy on Local Recurrence and Survival

Jayant S. Vaidya(University College London), Max Bulsara(University College London), Christobel Saunders(The University of Western Australia), Henrik Flyger(University of Copenhagen), Jeffrey Tobias(Royal London Hospital), Tammy Corica(Sir Charles Gairdner Hospital), Samuele Massarut(Centro di Riferimento Oncologico), Frederik Wenz(Heidelberg University), Steffi Pigorsch(Krankenhaus vom Roten Kreuz), Michael Alvarado(University of California, San Francisco), Michael Douek(University of Oxford), W. Eiermann(Krankenhaus vom Roten Kreuz), Chris Brew‐Graves(University College London), Norman Williams(University College London), Ingrid Potyka(University College London), Nicholas Roberts(University College London), Marcelle Bernstein(The Patients Association), Douglas Brown(Ninewells Hospital), Elena Sperk(Heidelberg University), Siobhan Laws(Royal Hampshire County Hospital), Marc Sütterlin(Heidelberg University), Steinar Lundgren(Norwegian University of Science and Technology), Dennis R. Holmes(University of Southern California), Lorenzo Vinante(Centro di Riferimento Oncologico), Fernando A. Bozza(Istituto Oncologico Veneto), Montserrat Pazos(Ludwig-Maximilians-Universität München), Magali Le Blanc‐Onfroy(Institut de Cancérologie de l'Ouest), Günther Gruber(Immunologie-Zentrum Zürich), Wojciech Polkowski(Medical University of Lublin), Konstantin J. Dedes(University Hospital of Zurich), Marcus Niewald(Saarland University), Jens‐Uwe Blohmer(Sankt Gertrauden Krankenhaus), David R. McCready(Princess Margaret Cancer Centre), Richard Hoefer, Pond R. Kelemen(New York Medical College), Gloria Petralia(Royal London Hospital), Mary Falzon(Royal London Hospital), Michael Baum(University College London), David Joseph(Sir Charles Gairdner Hospital)
JAMA Oncology
April 2, 2020
Cited by 106Open Access
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Abstract

Importance: Conventional adjuvant radiotherapy for breast cancer given daily for several weeks is onerous and expensive. Some patients may be obliged to choose a mastectomy instead, and some may forgo radiotherapy altogether. We proposed a clinical trial to test whether radiotherapy could be safely limited to the tumor bed. Objective: To determine whether delayed second-procedure targeted intraoperative radiotherapy (TARGIT-IORT) is noninferior to whole-breast external beam radiotherapy (EBRT) in terms of local control. Design, Setting, and Participants: In this prospective, randomized (1:1 ratio) noninferiority trial, 1153 patients aged 45 years or older with invasive ductal breast carcinoma smaller than 3.5 cm treated with breast conservation were enrolled from 28 centers in 9 countries. Data were locked in on July 3, 2019. Interventions: The TARGIT-A trial was started in March 2000; patients were randomized after needle biopsy to receive TARGIT-IORT immediately after lumpectomy under the same anesthetic vs EBRT and results have been shown to be noninferior. A parallel study, described in this article, was initiated in 2004; patients who had their cancer excised were randomly allocated using separate randomization tables to receive EBRT or delayed TARGIT-IORT given as a second procedure by reopening the lumpectomy wound. Main Outcomes and Measures: A noninferiority margin for local recurrence rate of 2.5% at 5 years, and long-term survival outcomes. Results: Overall, 581 women (mean [SD] age, 63 [7] years) were randomized to delayed TARGIT-IORT and 572 patients (mean [SD] age, 63 [8] years) were randomized to EBRT. Sixty patients (5%) had tumors larger than 2 cm, or had positive nodes and only 32 (2.7%) were younger than 50 years. Delayed TARGIT-IORT was not noninferior to EBRT. The local recurrence rates at 5-year complete follow-up were: delayed TARGIT-IORT vs EBRT (23/581 [3.96%] vs 6/572 [1.05%], respectively; difference, 2.91%; upper 90% CI, 4.4%). With long-term follow-up (median [IQR], 9.0 [7.5-10.5] years), there was no statistically significant difference in local recurrence-free survival (HR, 0.75; 95% CI, 0.57-1.003; P = .052), mastectomy-free survival (HR, 0.88; 95% CI, 0.65-1.18; P = .38), distant disease-free survival (HR, 1.00; 95% CI, 0.72-1.39; P = .98), or overall survival (HR, 0.96; 95% CI, 0.68-1.35; P = .80). Conclusions and Relevance: These long-term data show that despite an increase in the number of local recurrences with delayed TARGIT-IORT, there was no statistically significant decrease in mastectomy-free survival, distant disease-free survival, or overall survival. Trial Registration: ISRCTN34086741, ClinicalTrials.gov Identifier: NCT00983684.


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