Accelerated partial breast irradiation using sole interstitial multicatheter brachytherapy compared with whole-breast irradiation with boost for early breast cancer: 10-year results of a GEC-ESTRO randomised, phase 3, non-inferiority trial.


Journal

The Lancet. Oncology
ISSN: 1474-5488
Titre abrégé: Lancet Oncol
Pays: England
ID NLM: 100957246

Informations de publication

Date de publication:
03 2023
Historique:
received: 29 11 2022
revised: 13 01 2023
accepted: 13 01 2023
pubmed: 5 2 2023
medline: 4 3 2023
entrez: 4 2 2023
Statut: ppublish

Résumé

Several randomised, phase 3 trials have investigated the value of different techniques of accelerated partial breast irradiation (APBI) for patients with early breast cancer after breast-conserving surgery compared with whole-breast irradiation. In a phase 3 randomised trial, we evaluated whether APBI using multicatheter brachytherapy is non-inferior compared with whole-breast irradiation. Here, we present the 10-year follow-up results. We did a randomised, phase 3, non-inferiority trial at 16 hospitals and medical centres in Austria, Czech Republic, Germany, Hungary, Poland, Spain, and Switzerland. Patients aged 40 years or older with early invasive breast cancer or ductal carcinoma in situ treated with breast-conserving surgery were centrally randomly assigned (1:1) to receive either whole-breast irradiation or APBI using multicatheter brachytherapy. Whole-breast irradiation was delivered in 25 daily fractions of 50 Gy over 5 weeks, with a supplemental boost of 10 Gy to the tumour bed, and APBI was delivered as 30·1 Gy (seven fractions) and 32·0 Gy (eight fractions) of high-dose-rate brachytherapy in 5 days or as 50 Gy of pulsed-dose-rate brachytherapy over 5 treatment days. Neither patients nor investigators were masked to treatment allocation. The primary endpoint was ipsilateral local recurrence, analysed in the as-treated population; the non-inferiority margin for the recurrence rate difference (defined for 5-year results) was 3 percentage points. The trial is registered with ClinicalTrials.gov, NCT00402519; the trial is complete. Between April 20, 2004, and July 30, 2009, 1328 female patients were randomly assigned to whole breast irradiation (n=673) or APBI (n=655), of whom 551 in the whole-breast irradiation group and 633 in the APBI group were eligible for analysis. At a median follow-up of 10·36 years (IQR 9·12-11·28), the 10-year local recurrence rates were 1·58% (95% CI 0·37 to 2·8) in the whole-breast irradiation group and 3·51% (1·99 to 5·03) in the APBI group. The difference in 10-year rates between the groups was 1·93% (95% CI -0·018 to 3·87; p=0·074). Adverse events were mostly grade 1 and 2, in 234 (60%) of 393 participants in the whole-breast irradiation group and 314 (67%) of 470 participants in the APBI group, at 7·5-year or 10-year follow-up, or both. Patients in the APBI group had a significantly lower incidence of treatment-related grade 3 late side-effects than those in the whole-breast irradiation group (17 [4%] of 393 for whole-breast irradiation vs seven [1%] of 470 for APBI; p=0·021; at 7·5-year or 10-year follow-up, or both). At 10 years, the most common type of grade 3 adverse event in both treatment groups was fibrosis (six [2%] of 313 patients for whole-breast irradiation and three [1%] of 375 patients for APBI, p=0·56). No grade 4 adverse events or treatment-related deaths have been observed. Postoperative APBI using multicatheter brachytherapy after breast-conserving surgery in patients with early breast cancer is a valuable alternative to whole-breast irradiation in terms of treatment efficacy and is associated with fewer late side-effects. German Cancer Aid, Germany.

Sections du résumé

BACKGROUND
Several randomised, phase 3 trials have investigated the value of different techniques of accelerated partial breast irradiation (APBI) for patients with early breast cancer after breast-conserving surgery compared with whole-breast irradiation. In a phase 3 randomised trial, we evaluated whether APBI using multicatheter brachytherapy is non-inferior compared with whole-breast irradiation. Here, we present the 10-year follow-up results.
METHODS
We did a randomised, phase 3, non-inferiority trial at 16 hospitals and medical centres in Austria, Czech Republic, Germany, Hungary, Poland, Spain, and Switzerland. Patients aged 40 years or older with early invasive breast cancer or ductal carcinoma in situ treated with breast-conserving surgery were centrally randomly assigned (1:1) to receive either whole-breast irradiation or APBI using multicatheter brachytherapy. Whole-breast irradiation was delivered in 25 daily fractions of 50 Gy over 5 weeks, with a supplemental boost of 10 Gy to the tumour bed, and APBI was delivered as 30·1 Gy (seven fractions) and 32·0 Gy (eight fractions) of high-dose-rate brachytherapy in 5 days or as 50 Gy of pulsed-dose-rate brachytherapy over 5 treatment days. Neither patients nor investigators were masked to treatment allocation. The primary endpoint was ipsilateral local recurrence, analysed in the as-treated population; the non-inferiority margin for the recurrence rate difference (defined for 5-year results) was 3 percentage points. The trial is registered with ClinicalTrials.gov, NCT00402519; the trial is complete.
FINDINGS
Between April 20, 2004, and July 30, 2009, 1328 female patients were randomly assigned to whole breast irradiation (n=673) or APBI (n=655), of whom 551 in the whole-breast irradiation group and 633 in the APBI group were eligible for analysis. At a median follow-up of 10·36 years (IQR 9·12-11·28), the 10-year local recurrence rates were 1·58% (95% CI 0·37 to 2·8) in the whole-breast irradiation group and 3·51% (1·99 to 5·03) in the APBI group. The difference in 10-year rates between the groups was 1·93% (95% CI -0·018 to 3·87; p=0·074). Adverse events were mostly grade 1 and 2, in 234 (60%) of 393 participants in the whole-breast irradiation group and 314 (67%) of 470 participants in the APBI group, at 7·5-year or 10-year follow-up, or both. Patients in the APBI group had a significantly lower incidence of treatment-related grade 3 late side-effects than those in the whole-breast irradiation group (17 [4%] of 393 for whole-breast irradiation vs seven [1%] of 470 for APBI; p=0·021; at 7·5-year or 10-year follow-up, or both). At 10 years, the most common type of grade 3 adverse event in both treatment groups was fibrosis (six [2%] of 313 patients for whole-breast irradiation and three [1%] of 375 patients for APBI, p=0·56). No grade 4 adverse events or treatment-related deaths have been observed.
INTERPRETATION
Postoperative APBI using multicatheter brachytherapy after breast-conserving surgery in patients with early breast cancer is a valuable alternative to whole-breast irradiation in terms of treatment efficacy and is associated with fewer late side-effects.
FUNDING
German Cancer Aid, Germany.

Identifiants

pubmed: 36738756
pii: S1470-2045(23)00018-9
doi: 10.1016/S1470-2045(23)00018-9
pii:
doi:

Banques de données

ClinicalTrials.gov
['NCT00402519']

Types de publication

Randomized Controlled Trial Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

262-272

Informations de copyright

Copyright © 2023 Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of interests VS reports grant from German Cancer Aid during the conduct of the study. VS, CP, and TM report consultation fees from Nucletron Operations an Elekta Company, outside the submitted work. CP and TM report financial support for National Laboratories Excellence program (National Tumorbiology Laboratory project NLP-17 and the Hungarian Thematic Excellence Program (TKP2021-EGA-44), outside the submitted work. RF reports grants from Merck Serono, Astra Zeneca, MSD, Novocure, MBS, Siemens AG, AbbVie, and Fresenius Nutrition, and consultation fees from MSD, AstraZeneca, BMS, Novocure, Merck Serono, and payment for expert testimony from MSD, AstraZeneca, Novocure, BMS, and Merck Serono. All other authors declare no competing interests.

Auteurs

Vratislav Strnad (V)

Department of Radiation Oncology, University Hospital Erlangen and Comprehensive Cancer Center Erlangen-EMN, Erlangen, Germany. Electronic address: vratislav.strnad@uk-erlangen.de.

Csaba Polgár (C)

Center of Radiotherapy, National Institute of Oncology, Budapest, Hungary; Department of Oncology, Semmelweis University, Budapest, Hungary.

Oliver J Ott (OJ)

Department of Radiation Oncology, University Hospital Erlangen and Comprehensive Cancer Center Erlangen-EMN, Erlangen, Germany.

Guido Hildebrandt (G)

Department of Radiation Oncology, University Hospital Leipzig, Leipzig, Germany; Department of Radiation Oncology, University Hospital Rostock, Rostock, Germany.

Daniela Kauer-Dorner (D)

Department of Radiation Oncology, University Hospital AKH Wien, Vienna, Austria.

Hellen Knauerhase (H)

Department of Radiation Oncology, University Hospital Rostock, Rostock, Germany.

Tibor Major (T)

Center of Radiotherapy, National Institute of Oncology, Budapest, Hungary; Department of Oncology, Semmelweis University, Budapest, Hungary.

Jarosław Łyczek (J)

Brachytherapy Department, Centrum Onkologii-Instytut im Marii Skł odowskej, Warsaw, Poland; Podkarpacki Hospital Cancer Center Brzozów, Brzozów, Poland.

Jose Luis Guinot (JL)

Department of Radiation Oncology, Valencian Institute of Oncology Valencia, Valencia, Spain.

Cristina Gutierrez Miguelez (C)

Department of Radiation Oncology, Catalan Institute of Oncology, Barcelona, Spain.

Pavel Slampa (P)

Department of Radiation Oncology, Masaryk Memorial Cancer Institute, Brno, Czech Republic.

Michael Allgäuer (M)

Department of Radiation Oncology, Hospital Barmherzige Brüder Regensburg, Regensburg, Germany.

Kristina Lössl (K)

Department of Radiation Oncology, University Hospital Bern, Inselspital, Bern, Switzerland.

Bülent Polat (B)

Department of Radiation Oncology, University Hospital Würzburg, Würzburg, Germany.

Rainer Fietkau (R)

Department of Radiation Oncology, University Hospital Erlangen and Comprehensive Cancer Center Erlangen-EMN, Erlangen, Germany; Department of Radiation Oncology, University Hospital Rostock, Rostock, Germany.

Annika Schlamann (A)

Department of Radiation Oncology, University Hospital Leipzig, Leipzig, Germany.

Alexandra Resch (A)

Department of Radiation Oncology, University Hospital AKH Wien, Vienna, Austria.

Anna Kulik (A)

Brachytherapy Department, Centrum Onkologii-Instytut im Marii Skł odowskej, Warsaw, Poland.

Leo Arribas (L)

Department of Radiation Oncology, Valencian Institute of Oncology Valencia, Valencia, Spain.

Peter Niehoff (P)

Department of Radiation Oncology, University Hospital Kiel, Kiel, Germany; Department of Radiotherapy, Sana Clinic, Offenbach, Germany.

Ferran Guedea (F)

Department of Radiation Oncology, Catalan Institute of Oncology, Barcelona, Spain.

Jürgen Dunst (J)

Department of Radiation Oncology, University Hospital Kiel, Kiel, Germany.

Christine Gall (C)

Department of Medical Informatics, Biometry and Epidemiology, University Erlangen-Nuremberg, Nuremberg, Germany.

Wolfgang Uter (W)

Department of Medical Informatics, Biometry and Epidemiology, University Erlangen-Nuremberg, Nuremberg, Germany.

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