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Impact of denosumab on bone mass in cancer patients
Cancer therapy-induced bone loss (CTIBL) is a form of secondary osteoporosis associated with systemic chemotherapy and hormonal ablation therapy. The monitoring and treatment of CTIBL is an important component of comprehensive cancer care, especially for patients with curable disease and long life e...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3707483/ https://www.ncbi.nlm.nih.gov/pubmed/23861604 http://dx.doi.org/10.2147/CPAA.S30330 |
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author | Brown-Glaberman, Ursa Stopeck, Alison T |
author_facet | Brown-Glaberman, Ursa Stopeck, Alison T |
author_sort | Brown-Glaberman, Ursa |
collection | PubMed |
description | Cancer therapy-induced bone loss (CTIBL) is a form of secondary osteoporosis associated with systemic chemotherapy and hormonal ablation therapy. The monitoring and treatment of CTIBL is an important component of comprehensive cancer care, especially for patients with curable disease and long life expectancies. Whereas oral bisphosphonates remain the most commonly used therapeutic option for CTIBL, additional treatment options may be required for patients who do not respond adequately or are intolerant to bisphosphonates, have renal insufficiency, or are receiving treatment with nephrotoxic medications. For these patients, denosumab, a monoclonal antibody targeting the receptor activator of nuclear factor-κB ligand (RANKL), offers an effective and well-tolerated alternative. Several recent randomized trials have examined the use of denosumab as treatment for CTIBL associated with hormone ablation therapy for breast and prostate cancer. Recent data suggest a possible role for RANKL inhibitors in both chemoprevention and the prevention of cancer recurrence through direct effects on breast tissue and breast cancer stem cells. The outcomes of several international Phase III clinical trials currently underway will help clarify the role of denosumab in patients undergoing cancer therapy. |
format | Online Article Text |
id | pubmed-3707483 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-37074832013-07-16 Impact of denosumab on bone mass in cancer patients Brown-Glaberman, Ursa Stopeck, Alison T Clin Pharmacol Review Cancer therapy-induced bone loss (CTIBL) is a form of secondary osteoporosis associated with systemic chemotherapy and hormonal ablation therapy. The monitoring and treatment of CTIBL is an important component of comprehensive cancer care, especially for patients with curable disease and long life expectancies. Whereas oral bisphosphonates remain the most commonly used therapeutic option for CTIBL, additional treatment options may be required for patients who do not respond adequately or are intolerant to bisphosphonates, have renal insufficiency, or are receiving treatment with nephrotoxic medications. For these patients, denosumab, a monoclonal antibody targeting the receptor activator of nuclear factor-κB ligand (RANKL), offers an effective and well-tolerated alternative. Several recent randomized trials have examined the use of denosumab as treatment for CTIBL associated with hormone ablation therapy for breast and prostate cancer. Recent data suggest a possible role for RANKL inhibitors in both chemoprevention and the prevention of cancer recurrence through direct effects on breast tissue and breast cancer stem cells. The outcomes of several international Phase III clinical trials currently underway will help clarify the role of denosumab in patients undergoing cancer therapy. Dove Medical Press 2013-07-04 /pmc/articles/PMC3707483/ /pubmed/23861604 http://dx.doi.org/10.2147/CPAA.S30330 Text en © 2013 Brown-Glaberman and Stopeck, publisher and licensee Dove Medical Press Ltd This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited. |
spellingShingle | Review Brown-Glaberman, Ursa Stopeck, Alison T Impact of denosumab on bone mass in cancer patients |
title | Impact of denosumab on bone mass in cancer patients |
title_full | Impact of denosumab on bone mass in cancer patients |
title_fullStr | Impact of denosumab on bone mass in cancer patients |
title_full_unstemmed | Impact of denosumab on bone mass in cancer patients |
title_short | Impact of denosumab on bone mass in cancer patients |
title_sort | impact of denosumab on bone mass in cancer patients |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3707483/ https://www.ncbi.nlm.nih.gov/pubmed/23861604 http://dx.doi.org/10.2147/CPAA.S30330 |
work_keys_str_mv | AT brownglabermanursa impactofdenosumabonbonemassincancerpatients AT stopeckalisont impactofdenosumabonbonemassincancerpatients |