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Evaluating the efficacy of preoperative radiotherapy in breast cancer patients non-responsive to neoadjuvant chemotherapy: A clinical trial

Mahmut Muslumanoglu 1 ORCID logo
Enver Ozkurt 2 ORCID logo
Selman Emiroglu 1, * ORCID logo
Kamuran Ibis 3 ORCID logo
Asmaa Abuaisha 4 ORCID logo
Mustafa Tukenmez 1 ORCID logo
Neslihan Cabioglu 5 ORCID logo
Abdullah Igci 1 ORCID logo
Vahit Ozmen 1 ORCID logo
Nezihe Seden Kucucuk 3 ORCID logo
  1. Breast Surgery Division, Department of General Surgery, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey
  2. Department of General Surgery, Basari Hospital, Istanbul, Turkey
  3. Department of Radiation Oncology, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey
  4. Biruni University Research Center, Biruni University, Istanbul, Turkey
  5. reast Surgery Division, Department of General Surgery, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey
Correspondence to: Selman Emiroglu, Breast Surgery Division, Department of General Surgery, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey. ORCID: https://orcid.org/0000-0001-9333-6926. Email: [email protected].
Volume & Issue: Vol. 11 No. 12 (2024) | Page No.: 6978-6988 | DOI: 10.15419/bmrat.v11i12.944
Published: 2024-12-31

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This article is published with open access by BioMedPress. This article is distributed under the terms of the Creative Commons Attribution License (CC-BY 4.0) which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited. 

Abstract

Introduction: Neoadjuvant chemotherapy (NACT) is a prevalent treatment strategy for patients with locally advanced breast cancer (LABC). Achieving a pathologic complete response (pCR) is a critical determinant of favorable outcomes. To enhance response rates, some clinicians have incorporated radiotherapy (RT) prior to surgery.

Methods: This observational cohort study aimed to investigate the initial outcomes and complication rates of preoperative radiotherapy (PRT) in breast cancer (BC) patients who did not achieve a complete response post-NACT. Between January 2017 and January 2020, 216 patients who were clinical T1-3, lymph node-positive, non-metastatic, and received NACT were analyzed. After the final dose of chemotherapy, patients were evaluated clinically and radiologically. Among them, 123 patients were non-complete responders. Of these, 37 patients received PRT according to the guidelines.

Results: Following PRT and surgery, 7 (18.9%) patients showed pCR in the breast and 14 (37.8%) in the axilla. HER2-positive and triple-negative breast cancer (TNBC) patients were significantly associated with complete response following PRT in the breast and axilla (p = 0.029). Post-surgical infection was detected in 11 (29.7%) patients, with factors such as a body mass index greater than 25 kg/m2 significantly affecting surgical site infection rates (p = 0.036). The implant loss rate was 16.7% (n = 2), and there was no grade 3 or higher RT-related skin toxicity.

Conclusion: This study demonstrated that PRT for non-complete responder patients improves pCR rates in the breast and axilla, allowing almost 38% of patients to have successful breast-conserving surgery, and lowering axillary lymph-node dissection rates without an increase in major complications. Clinical trials: ClinicalTrials.gov: NCT05274594.

 

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