Outcomes from a mechanistic biomarker multi-arm and randomised study of liposomal MTP-PE (Mifamurtide) in metastatic and/or recurrent osteosarcoma (EuroSarc-Memos trial)
David J. Barnes,
Peter Dutton,
Øyvind Bruland,
Hans Gelderblom,
Ade Faleti,
Claudia Bühnemann,
Annemiek van Maldegem,
Hannah Johnson,
Lisa Poulton,
Sharon Love,
Gesa Tiemeier,
Els van Beelen,
Karin Herbschleb,
Caroline Haddon,
Lucinda Billingham,
Kevin Bradley,
Stefano Ferrari,
Emanuela Palmerini,
Piero Picci,
Uta Dirksen,
Sandra J. Strauss,
Pancras C. W. Hogendoorn,
Emmeline Buddingh,
Jean-Yves Blay,
Anne Marie Cleton-Jansen,
Andrew Bassim Hassan
Affiliations
David J. Barnes
Oxford Molecular Pathology Institute, Sir William Dunn School of Pathology, University of Oxford, South Parks Road, and Oxford University Hospital NHS Trust
Peter Dutton
Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences and Centre for Statistics in Medicine (CSM), University of Oxford, Botnar Research Centre
Øyvind Bruland
Institute of Clinical Medicine, Faculty of Medicine, University of Oslo and Department of Oncology-Norwegian Radium Hospital, Oslo University Hospital
Hans Gelderblom
Leiden University Medical Center
Ade Faleti
Department of Oncology Early Phase trials unit and Oncology Clinical Trials Office (OCTO), University of Oxford, Old Road Campus Research Building
Claudia Bühnemann
Oxford Molecular Pathology Institute, Sir William Dunn School of Pathology, University of Oxford, South Parks Road, and Oxford University Hospital NHS Trust
Annemiek van Maldegem
Oxford Molecular Pathology Institute, Sir William Dunn School of Pathology, University of Oxford, South Parks Road, and Oxford University Hospital NHS Trust
Hannah Johnson
Department of Oncology Early Phase trials unit and Oncology Clinical Trials Office (OCTO), University of Oxford, Old Road Campus Research Building
Lisa Poulton
Department of Oncology Early Phase trials unit and Oncology Clinical Trials Office (OCTO), University of Oxford, Old Road Campus Research Building
Sharon Love
Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences and Centre for Statistics in Medicine (CSM), University of Oxford, Botnar Research Centre
Gesa Tiemeier
Oxford Molecular Pathology Institute, Sir William Dunn School of Pathology, University of Oxford, South Parks Road, and Oxford University Hospital NHS Trust
Els van Beelen
Leiden University Medical Center
Karin Herbschleb
Department of Oncology Early Phase trials unit and Oncology Clinical Trials Office (OCTO), University of Oxford, Old Road Campus Research Building
Caroline Haddon
Department of Oncology Early Phase trials unit and Oncology Clinical Trials Office (OCTO), University of Oxford, Old Road Campus Research Building
Lucinda Billingham
Cancer Research Clinical Trials Unit (Cancer Sciences), Institute of Cancer and Genomic Sciences, Robert Aitken Building, University of Birmingham
Kevin Bradley
Department of Radiology, Churchill Hospital, Oxford University Hospitals Foundation Trust
Stefano Ferrari
Istituti Ortopedici Rizzoli
Emanuela Palmerini
Istituti Ortopedici Rizzoli
Piero Picci
Istituti Ortopedici Rizzoli
Uta Dirksen
Pediatrics III, West German Cancer Centre Network Essen-Muenster, University Hospital Essen
Sandra J. Strauss
Department of Oncology, UCLH NHS Foundation Trust
Pancras C. W. Hogendoorn
Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences and Centre for Statistics in Medicine (CSM), University of Oxford, Botnar Research Centre
Emmeline Buddingh
Leiden University Medical Center
Jean-Yves Blay
Universitè Lyon 1 Claude Bernard
Anne Marie Cleton-Jansen
Leiden University Medical Center
Andrew Bassim Hassan
Oxford Molecular Pathology Institute, Sir William Dunn School of Pathology, University of Oxford, South Parks Road, and Oxford University Hospital NHS Trust
Abstract The phase III clinical study of adjuvant liposomal muramyl tripeptide (MTP-PE) in resected high-grade osteosarcoma (OS) documented positive results that have been translated into regulatory approval, supporting initial promise for innate immune therapies in OS. There remains, however, no new approved treatment such as MTP-PE for either metastatic or recurrent OS. Whilst the addition of different agents, including liposomal MTP-PE, to surgery for metastatic or recurrent high-grade osteosarcoma has tried to improve response rates, a mechanistic hiatus exists in terms of a detailed understanding the therapeutic strategies required in advanced disease. Here we report a Bayesian designed multi-arm, multi-centre, open-label phase II study with randomisation in patients with metastatic and/or recurrent OS, designed to investigate how patients with OS might respond to liposomal MTP-PE, either given alone or in combination with ifosfamide. Despite the trial closing because of poor recruitment within the allocated funding period, with no objective responses in eight patients, we report the design and feasibility outcomes for patients registered into the trial. We demonstrate the feasibility of the Bayesian design, European collaboration, tissue collection with genomic analysis and serum cytokine characterisation. Further mechanistic investigation of liposomal MTP-PE alone and in combination with other agents remains warranted in metastatic OS.