Single pre-operative radiation therapy (SPORT-CK) trial for low-risk breast cancer: Early results of a phase 2 study.

Breast cancer Partial breast irradiation Preoperative radiotherapy VMAT

Journal

Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology
ISSN: 1879-0887
Titre abrégé: Radiother Oncol
Pays: Ireland
ID NLM: 8407192

Informations de publication

Date de publication:
30 Aug 2024
Historique:
received: 16 03 2024
revised: 15 08 2024
accepted: 21 08 2024
medline: 2 9 2024
pubmed: 2 9 2024
entrez: 1 9 2024
Statut: aheadofprint

Résumé

Preoperative partial breast irradiation (PBI) is a novel technique that can be used in patients with early-stage breast cancer with the goal of limiting the irradiated breast volume, toxicity and number of fractions. The aim of this trial is to assess the toxicity, surgical, oncologic and cosmetic outcomes of preoperative PBI. In this single-arm phase II trial, we enrolled women ≥ 60 years, with unifocal low-risk breast invasive ductal carcinoma (cT1N0, grade 1-2, ER+, Her2-). Patients were treated with a single fraction of 20 Gy of preoperative PBI using volumetric modulated arc therapy (VMAT). Patients then underwent breast-conserving surgery (BCS) +/- sentinel lymph node biopsy within 72 h of radiation. Primary outcomes were rate of surgical complications and early toxicity. Secondary outcomes were cosmesis at 12 months, chronic toxicity and ipsilateral breast tumor recurrence. Twenty-five patients were recruited with a median age of 67 years, and a median follow-up of 60 months. Sentinel biopsy was positive in 1 out of 24 patients (4 %). Two patients received adjuvant RT for close margins or positive lymph nodes. Within the first 90 days, none of the patients had surgical complications; almost all had grade 0 to 1 acute and late RTOG skin toxicity. The cosmetic outcome was rated between good and excellent in all cases by physicians and patients, except for one patient who self-rated her cosmesis as fair as of the third year. There were no recurrences. Preoperative single-fraction PBI is a safe and feasible treatment for elderly patients with low-risk early-stage breast cancer, with no surgical complications, very low rates of acute and late radiation toxicity, and excellent cosmetic outcomes. Randomized controlled trials are needed to compare preoperative to adjuvant PBI in this patient population.

Sections du résumé

BACKGROUND AND PURPOSE OBJECTIVE
Preoperative partial breast irradiation (PBI) is a novel technique that can be used in patients with early-stage breast cancer with the goal of limiting the irradiated breast volume, toxicity and number of fractions. The aim of this trial is to assess the toxicity, surgical, oncologic and cosmetic outcomes of preoperative PBI.
MATERIALS AND METHODS METHODS
In this single-arm phase II trial, we enrolled women ≥ 60 years, with unifocal low-risk breast invasive ductal carcinoma (cT1N0, grade 1-2, ER+, Her2-). Patients were treated with a single fraction of 20 Gy of preoperative PBI using volumetric modulated arc therapy (VMAT). Patients then underwent breast-conserving surgery (BCS) +/- sentinel lymph node biopsy within 72 h of radiation. Primary outcomes were rate of surgical complications and early toxicity. Secondary outcomes were cosmesis at 12 months, chronic toxicity and ipsilateral breast tumor recurrence.
RESULTS RESULTS
Twenty-five patients were recruited with a median age of 67 years, and a median follow-up of 60 months. Sentinel biopsy was positive in 1 out of 24 patients (4 %). Two patients received adjuvant RT for close margins or positive lymph nodes. Within the first 90 days, none of the patients had surgical complications; almost all had grade 0 to 1 acute and late RTOG skin toxicity. The cosmetic outcome was rated between good and excellent in all cases by physicians and patients, except for one patient who self-rated her cosmesis as fair as of the third year. There were no recurrences.
CONCLUSION CONCLUSIONS
Preoperative single-fraction PBI is a safe and feasible treatment for elderly patients with low-risk early-stage breast cancer, with no surgical complications, very low rates of acute and late radiation toxicity, and excellent cosmetic outcomes. Randomized controlled trials are needed to compare preoperative to adjuvant PBI in this patient population.

Identifiants

pubmed: 39218040
pii: S0167-8140(24)03488-1
doi: 10.1016/j.radonc.2024.110510
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

110510

Informations de copyright

Copyright © 2024 The Author(s). Published by Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Dima Mahmoud (D)

Division of Radiation Oncology, McGill University Health Centre, Montreal, Canada.

Michael Yassa (M)

Division of Radiation Oncology, Hôpital Maisonneuve-Rosemont, Montreal, Canada.

Leticia Alvarado (L)

Division of Radiation Oncology, McGill University Health Centre, Montreal, Canada.

Christine Lambert (C)

Division of Radiation Oncology, McGill University Health Centre, Montreal, Canada; Gerald Bronfman Department of Oncology, McGill University, Montreal, Canada.

Sarkis Meterissian (S)

Gerald Bronfman Department of Oncology, McGill University, Montreal, Canada; Department of Surgery, McGill University, Montreal, Canada.

Dawn Anderson (D)

Gerald Bronfman Department of Oncology, McGill University, Montreal, Canada; Department of Surgery, McGill University, Montreal, Canada.

Francine Tremblay (F)

Gerald Bronfman Department of Oncology, McGill University, Montreal, Canada; Department of Surgery, McGill University, Montreal, Canada.

Naim Otaky (N)

Department of Surgery, McGill University, Montreal, Canada.

John Keyserlingk (J)

Department of Surgery, McGill University, Montreal, Canada.

Valerie Panet-Raymond (V)

Division of Radiation Oncology, McGill University Health Centre, Montreal, Canada; Gerald Bronfman Department of Oncology, McGill University, Montreal, Canada.

Neil Kopek (N)

Division of Radiation Oncology, McGill University Health Centre, Montreal, Canada; Gerald Bronfman Department of Oncology, McGill University, Montreal, Canada.

Marc David (M)

Division of Radiation Oncology, McGill University Health Centre, Montreal, Canada; Gerald Bronfman Department of Oncology, McGill University, Montreal, Canada.

Marie Duclos (M)

Division of Radiation Oncology, McGill University Health Centre, Montreal, Canada; Gerald Bronfman Department of Oncology, McGill University, Montreal, Canada.

Catherine Pembroke (C)

Department of Clinical Oncology, Velindre Cancer Centre, Cardiff, United Kingdom.

David Fleiszer (D)

Gerald Bronfman Department of Oncology, McGill University, Montreal, Canada; Department of Surgery, McGill University, Montreal, Canada.

Ari N Meguerditchian (AN)

Gerald Bronfman Department of Oncology, McGill University, Montreal, Canada; Department of Surgery, McGill University, Montreal, Canada.

Antoine Loutfi (A)

Gerald Bronfman Department of Oncology, McGill University, Montreal, Canada; Department of Surgery, McGill University, Montreal, Canada.

Danny Lavigne (D)

Division of Radiation Oncology, Hôpital Maisonneuve-Rosemont, Montreal, Canada.

Tarek Hijal (T)

Division of Radiation Oncology, McGill University Health Centre, Montreal, Canada; Gerald Bronfman Department of Oncology, McGill University, Montreal, Canada. Electronic address: tarek.hijal@muhc.mcgill.ca.

Classifications MeSH