Metastases-directed Radiotherapy in Addition to Standard Systemic Therapy in Patients with Oligometastatic Breast Cancer: Study protocol for a randomized controlled multi-national and multi-center clinical trial (OLIGOMA).

Metastatic breast cancer Progression-free survival Quality of life Radiosurgery Stereotactic ablative radiotherapy Stereotactic body radiotherapy

Journal

Clinical and translational radiation oncology
ISSN: 2405-6308
Titre abrégé: Clin Transl Radiat Oncol
Pays: Ireland
ID NLM: 101713416

Informations de publication

Date de publication:
May 2021
Historique:
received: 29 12 2020
revised: 27 03 2021
accepted: 29 03 2021
entrez: 29 4 2021
pubmed: 30 4 2021
medline: 30 4 2021
Statut: epublish

Résumé

Several recent randomized therapeutic exploratory trials demonstrated improvement of progression-free survival and in some even overall survival using stereotactic body radiotherapy in patients with oligometastatic disease. However, only very few patients enrolled in these trials had breast cancer, and results from confirmatory trials are lacking. The OLIGOMA-trial is a randomized controlled multi-national multi-center therapeutic confirmatory trial studying the role of local ablative radiotherapy as an additive treatment in patients with oligometastatic breast cancer receiving standard systemic therapy. Patients will be randomized 1:1 to standard systemic therapy according to national guidelines with or without radiotherapy to all metastatic sites. Randomization will be stratified according to type and line of systemic therapy, which has to be determined by a multidisciplinary tumor board before enrollment. Patients with up to five metastatic lesions are eligible, including patients with up to three brain metastases (only in case of extracranial disease) and with locoregional recurrence (only in case of additional metastatic lesions). In the standard arm, palliative radiotherapy to symptomatic metastases is permitted if at least one lesion remains untreated. The co-primary endpoints are progression-free survival and quality of life. The primary hypothesis is that progression-free survival in the experimental arm will be superior to the standard arm while simultaneously demonstrating non-inferiority of quality of life at 12 weeks after randomization. Secondary endpoints are feasibility, overall survival, toxicity, quality of life and patient satisfaction. A translational sub-study with collection of ctDNA will be conducted. The OLIGOMA-trial will provide high level evidence on the use of and benefit from local ablative radiotherapy for patients with oligometastatic breast cancer. The OLIGOMA-trial is registered at clinicialtrials.gov under the identification NCT04495309. The related information was first posted on July 31st 2020.

Sections du résumé

BACKGROUND BACKGROUND
Several recent randomized therapeutic exploratory trials demonstrated improvement of progression-free survival and in some even overall survival using stereotactic body radiotherapy in patients with oligometastatic disease. However, only very few patients enrolled in these trials had breast cancer, and results from confirmatory trials are lacking.
METHODS/DESIGN METHODS
The OLIGOMA-trial is a randomized controlled multi-national multi-center therapeutic confirmatory trial studying the role of local ablative radiotherapy as an additive treatment in patients with oligometastatic breast cancer receiving standard systemic therapy. Patients will be randomized 1:1 to standard systemic therapy according to national guidelines with or without radiotherapy to all metastatic sites. Randomization will be stratified according to type and line of systemic therapy, which has to be determined by a multidisciplinary tumor board before enrollment. Patients with up to five metastatic lesions are eligible, including patients with up to three brain metastases (only in case of extracranial disease) and with locoregional recurrence (only in case of additional metastatic lesions). In the standard arm, palliative radiotherapy to symptomatic metastases is permitted if at least one lesion remains untreated. The co-primary endpoints are progression-free survival and quality of life. The primary hypothesis is that progression-free survival in the experimental arm will be superior to the standard arm while simultaneously demonstrating non-inferiority of quality of life at 12 weeks after randomization. Secondary endpoints are feasibility, overall survival, toxicity, quality of life and patient satisfaction. A translational sub-study with collection of ctDNA will be conducted.
DISCUSSION CONCLUSIONS
The OLIGOMA-trial will provide high level evidence on the use of and benefit from local ablative radiotherapy for patients with oligometastatic breast cancer.
TRIAL REGISTRATION BACKGROUND
The OLIGOMA-trial is registered at clinicialtrials.gov under the identification NCT04495309. The related information was first posted on July 31st 2020.

Identifiants

pubmed: 33912695
doi: 10.1016/j.ctro.2021.03.012
pii: S2405-6308(21)00035-5
pmc: PMC8065185
doi:

Banques de données

ClinicalTrials.gov
['NCT04495309']

Types de publication

Journal Article

Langues

eng

Pagination

90-96

Informations de copyright

© 2021 The Authors.

Déclaration de conflit d'intérêts

DK has received honoraria from Merck Sharp & Dome outside the submitted work. The other 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.

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Auteurs

David Krug (D)

Klinik für Strahlentherapie, Universitätsklinikum Schleswig-Holstein, Kiel, Deutschland.

Reinhard Vonthein (R)

Institut für Medizinische Biometrie und Statistik, Universität zu Lübeck, Universitätsklinikum Schleswig-Holstein, Campus Lübeck, Lübeck, Deutschland.

Alicia Illen (A)

ZKS Lübeck, Universität zu Lübeck, Lübeck, Deutschland.

Denise Olbrich (D)

ZKS Lübeck, Universität zu Lübeck, Lübeck, Deutschland.

Jörg Barkhausen (J)

Klinik für Radiologie und Nuklearmedizin, Universitätsklinikum Schleswig-Holstein, Lübeck, Deutschland.

Julia Richter (J)

Sektion für Hämatopathologie, Institut für Pathologie, Universitätsklinikum Schleswig-Holstein, Kiel, Deutschland.

Wolfram Klapper (W)

Sektion für Hämatopathologie, Institut für Pathologie, Universitätsklinikum Schleswig-Holstein, Kiel, Deutschland.

Claudia Schmalz (C)

Klinik für Strahlentherapie, Universitätsklinikum Schleswig-Holstein, Kiel, Deutschland.

Achim Rody (A)

Klinik für Frauenheilkunde und Geburtshilfe, Universitätsklinikum Schleswig-Holstein, Lübeck, Deutschland.

Nicolai Maass (N)

Klinik für Gynäkologie und Geburtshilfe, Universitätsklinikum Schleswig-Holstein, Kiel, Deutschland.

Dirk Bauerschlag (D)

Klinik für Gynäkologie und Geburtshilfe, Universitätsklinikum Schleswig-Holstein, Kiel, Deutschland.

Nicole Heßler (N)

Institut für Medizinische Biometrie und Statistik, Universität zu Lübeck, Universitätsklinikum Schleswig-Holstein, Campus Lübeck, Lübeck, Deutschland.

Inke R König (IR)

Institut für Medizinische Biometrie und Statistik, Universität zu Lübeck, Universitätsklinikum Schleswig-Holstein, Campus Lübeck, Lübeck, Deutschland.

Kathrin Dellas (K)

Klinik für Strahlentherapie, Universitätsklinikum Schleswig-Holstein, Kiel, Deutschland.

Jürgen Dunst (J)

Klinik für Strahlentherapie, Universitätsklinikum Schleswig-Holstein, Kiel, Deutschland.

Classifications MeSH