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Efaproxiral red blood cell concentration predicts efficacy in patients with brain metastases

Efaproxiral (Efaproxyn™, RSR13), a synthetic allosteric modifier of haemoglobin (Hb), decreases Hb-oxygen (O(2)) binding affinity and enhances oxygenation of hypoxic tumours during radiation therapy. This analysis evaluated the Phase 3, Radiation Enhancing Allosteric Compound for Hypoxic Brain Metas...

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Autores principales: Stea, B, Shaw, E, Pintér, T, Hackman, J, Craig, M, May, J, Steffen, R P, Suh, J H
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2361352/
https://www.ncbi.nlm.nih.gov/pubmed/16773073
http://dx.doi.org/10.1038/sj.bjc.6603169
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author Stea, B
Shaw, E
Pintér, T
Hackman, J
Craig, M
May, J
Steffen, R P
Suh, J H
author_facet Stea, B
Shaw, E
Pintér, T
Hackman, J
Craig, M
May, J
Steffen, R P
Suh, J H
author_sort Stea, B
collection PubMed
description Efaproxiral (Efaproxyn™, RSR13), a synthetic allosteric modifier of haemoglobin (Hb), decreases Hb-oxygen (O(2)) binding affinity and enhances oxygenation of hypoxic tumours during radiation therapy. This analysis evaluated the Phase 3, Radiation Enhancing Allosteric Compound for Hypoxic Brain Metastases; RT-009 (REACH) study efficacy results in relation to efaproxiral exposure (efaproxiral red blood cell concentration (E-RBC) and number of doses). Recursive partitioning analysis Class I or II patients with brain metastases from solid tumours received standard whole-brain radiation therapy (3 Gy/fraction × 10 days), plus supplemental O(2) (4 l/min), either with efaproxiral (75 or 100 mg/kg daily) or without (control). Efaproxiral red blood cell concentrations were linearly extrapolated to all efaproxiral doses received. Three patient populations were analysed: (1) all eligible, (2) non-small-cell lung cancer (NSCLC) as primary cancer, and (3) breast cancer primary. Efficacy endpoints were survival and response rate. Brain metastases patients achieving sufficient E-RBC (⩾483 μg/ml) and receiving at least seven of 10 efaproxiral doses were most likely to experience survival and response benefits. Patients with breast cancer primary tumours generally achieved the target efaproxiral exposure and therefore gained greater benefit from efaproxiral treatment than NSCLC patients. This analysis defined the efaproxiral concentration-dependence in survival and response rate improvement, and provided a clearer understanding of efaproxiral dosing requirements.
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spelling pubmed-23613522009-09-10 Efaproxiral red blood cell concentration predicts efficacy in patients with brain metastases Stea, B Shaw, E Pintér, T Hackman, J Craig, M May, J Steffen, R P Suh, J H Br J Cancer Clinical Study Efaproxiral (Efaproxyn™, RSR13), a synthetic allosteric modifier of haemoglobin (Hb), decreases Hb-oxygen (O(2)) binding affinity and enhances oxygenation of hypoxic tumours during radiation therapy. This analysis evaluated the Phase 3, Radiation Enhancing Allosteric Compound for Hypoxic Brain Metastases; RT-009 (REACH) study efficacy results in relation to efaproxiral exposure (efaproxiral red blood cell concentration (E-RBC) and number of doses). Recursive partitioning analysis Class I or II patients with brain metastases from solid tumours received standard whole-brain radiation therapy (3 Gy/fraction × 10 days), plus supplemental O(2) (4 l/min), either with efaproxiral (75 or 100 mg/kg daily) or without (control). Efaproxiral red blood cell concentrations were linearly extrapolated to all efaproxiral doses received. Three patient populations were analysed: (1) all eligible, (2) non-small-cell lung cancer (NSCLC) as primary cancer, and (3) breast cancer primary. Efficacy endpoints were survival and response rate. Brain metastases patients achieving sufficient E-RBC (⩾483 μg/ml) and receiving at least seven of 10 efaproxiral doses were most likely to experience survival and response benefits. Patients with breast cancer primary tumours generally achieved the target efaproxiral exposure and therefore gained greater benefit from efaproxiral treatment than NSCLC patients. This analysis defined the efaproxiral concentration-dependence in survival and response rate improvement, and provided a clearer understanding of efaproxiral dosing requirements. Nature Publishing Group 2006-06-19 2006-06-13 /pmc/articles/PMC2361352/ /pubmed/16773073 http://dx.doi.org/10.1038/sj.bjc.6603169 Text en Copyright © 2006 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Clinical Study
Stea, B
Shaw, E
Pintér, T
Hackman, J
Craig, M
May, J
Steffen, R P
Suh, J H
Efaproxiral red blood cell concentration predicts efficacy in patients with brain metastases
title Efaproxiral red blood cell concentration predicts efficacy in patients with brain metastases
title_full Efaproxiral red blood cell concentration predicts efficacy in patients with brain metastases
title_fullStr Efaproxiral red blood cell concentration predicts efficacy in patients with brain metastases
title_full_unstemmed Efaproxiral red blood cell concentration predicts efficacy in patients with brain metastases
title_short Efaproxiral red blood cell concentration predicts efficacy in patients with brain metastases
title_sort efaproxiral red blood cell concentration predicts efficacy in patients with brain metastases
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2361352/
https://www.ncbi.nlm.nih.gov/pubmed/16773073
http://dx.doi.org/10.1038/sj.bjc.6603169
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