CApecitabine plus Radium-223 (Xofigo™) in breast cancer patients with BONe metastases (CARBON): study protocol for a phase IB/IIA randomised controlled trial
Abstract Background A substantial proportion of breast cancer patients develop metastatic disease, with over 450,000 deaths globally per year. Bone is the most common first site of metastatic disease accounting for 40% of all first recurrence and 70% of patients with advanced disease develop skeleta...
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doaj-f23455173b0d42049b53d3ddcd09b49b2021-01-17T12:29:29ZengBMCTrials1745-62152020-01-0121111010.1186/s13063-019-3643-6CApecitabine plus Radium-223 (Xofigo™) in breast cancer patients with BONe metastases (CARBON): study protocol for a phase IB/IIA randomised controlled trialRob Coleman0Janet Brown1Emma Rathbone2Louise Flanagan3Amber Reid4Jessica Kendall5Sacha Howell6Chris Twelves7Carlo Palmieri8Anjana Anand9Iain MacPherson10Sarah Brown11The University of SheffieldThe University of SheffieldCalderdale and Huddersfield NHS Foundation TrustClinical Trials Research Unit, Leeds Institute of Clinical Trials Research, University of LeedsClinical Trials Research Unit, Leeds Institute of Clinical Trials Research, University of LeedsClinical Trials Research Unit, Leeds Institute of Clinical Trials Research, University of LeedsThe Christie NHS Foundation TrustSt James’s University HospitalClatterbridge Cancer Centre NHS Foundation TrustNottingham University Hospitals NHS TrustInstitute of Cancer Sciences, University of GlasgowClinical Trials Research Unit, Leeds Institute of Clinical Trials Research, University of LeedsAbstract Background A substantial proportion of breast cancer patients develop metastatic disease, with over 450,000 deaths globally per year. Bone is the most common first site of metastatic disease accounting for 40% of all first recurrence and 70% of patients with advanced disease develop skeletal involvement. Treatment of bone metastases currently focusses on symptom relief and prevention and treatment of skeletal complications. However, there remains a need for further treatment options for patients with bone metastases. Combining systemic therapy with a bone-targeted agent, such as radium-223, may provide an effective treatment with minimal additional side effects. Methods/design CARBON is a UK-based, open-label, multi-centre study which comprises an initial safety phase to establish the feasibility and safety of combining radium-223 given on a 6-weekly schedule in combination with orally administered capecitabine followed by a randomised extension phase to further characterise the safety profile and provide preliminary estimation of efficacy. Discussion The CARBON study is important as the results will be the first to assess radium-223 with chemotherapy in advanced breast cancer. If the results find acceptable rates of toxicity with a decrease in bone turnover markers, further work will be necessary in a phase II/III setting to assess the efficacy and clinical benefit. Trial registration ISRCTN, ISRCTN92755158, Registered on 17 February 2016.https://doi.org/10.1186/s13063-019-3643-6Radium-223CapecitabineBone metastasesBone turnover markersBreast cancer |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Rob Coleman Janet Brown Emma Rathbone Louise Flanagan Amber Reid Jessica Kendall Sacha Howell Chris Twelves Carlo Palmieri Anjana Anand Iain MacPherson Sarah Brown |
spellingShingle |
Rob Coleman Janet Brown Emma Rathbone Louise Flanagan Amber Reid Jessica Kendall Sacha Howell Chris Twelves Carlo Palmieri Anjana Anand Iain MacPherson Sarah Brown CApecitabine plus Radium-223 (Xofigo™) in breast cancer patients with BONe metastases (CARBON): study protocol for a phase IB/IIA randomised controlled trial Trials Radium-223 Capecitabine Bone metastases Bone turnover markers Breast cancer |
author_facet |
Rob Coleman Janet Brown Emma Rathbone Louise Flanagan Amber Reid Jessica Kendall Sacha Howell Chris Twelves Carlo Palmieri Anjana Anand Iain MacPherson Sarah Brown |
author_sort |
Rob Coleman |
title |
CApecitabine plus Radium-223 (Xofigo™) in breast cancer patients with BONe metastases (CARBON): study protocol for a phase IB/IIA randomised controlled trial |
title_short |
CApecitabine plus Radium-223 (Xofigo™) in breast cancer patients with BONe metastases (CARBON): study protocol for a phase IB/IIA randomised controlled trial |
title_full |
CApecitabine plus Radium-223 (Xofigo™) in breast cancer patients with BONe metastases (CARBON): study protocol for a phase IB/IIA randomised controlled trial |
title_fullStr |
CApecitabine plus Radium-223 (Xofigo™) in breast cancer patients with BONe metastases (CARBON): study protocol for a phase IB/IIA randomised controlled trial |
title_full_unstemmed |
CApecitabine plus Radium-223 (Xofigo™) in breast cancer patients with BONe metastases (CARBON): study protocol for a phase IB/IIA randomised controlled trial |
title_sort |
capecitabine plus radium-223 (xofigo™) in breast cancer patients with bone metastases (carbon): study protocol for a phase ib/iia randomised controlled trial |
publisher |
BMC |
series |
Trials |
issn |
1745-6215 |
publishDate |
2020-01-01 |
description |
Abstract Background A substantial proportion of breast cancer patients develop metastatic disease, with over 450,000 deaths globally per year. Bone is the most common first site of metastatic disease accounting for 40% of all first recurrence and 70% of patients with advanced disease develop skeletal involvement. Treatment of bone metastases currently focusses on symptom relief and prevention and treatment of skeletal complications. However, there remains a need for further treatment options for patients with bone metastases. Combining systemic therapy with a bone-targeted agent, such as radium-223, may provide an effective treatment with minimal additional side effects. Methods/design CARBON is a UK-based, open-label, multi-centre study which comprises an initial safety phase to establish the feasibility and safety of combining radium-223 given on a 6-weekly schedule in combination with orally administered capecitabine followed by a randomised extension phase to further characterise the safety profile and provide preliminary estimation of efficacy. Discussion The CARBON study is important as the results will be the first to assess radium-223 with chemotherapy in advanced breast cancer. If the results find acceptable rates of toxicity with a decrease in bone turnover markers, further work will be necessary in a phase II/III setting to assess the efficacy and clinical benefit. Trial registration ISRCTN, ISRCTN92755158, Registered on 17 February 2016. |
topic |
Radium-223 Capecitabine Bone metastases Bone turnover markers Breast cancer |
url |
https://doi.org/10.1186/s13063-019-3643-6 |
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