| Literature DB >> 32835531 |
Emanuela Dell'Aquila1, Grazia Armento1, Michele Iuliani1, Sonia Simonetti1, Loretta D'Onofrio1, Tea Zeppola1, Cristina Madaudo1, Marco Russano1, Fabrizio Citarella1, Giulia Ribelli1, Francesco Pantano1, Bruno Vincenzi1, Giuseppe Tonini1, Daniele Santini1.
Abstract
INTRODUCTION: Prolonged use of anti-cancer treatments in breast and prostate tumors alters physiological bone turnover leading to adverse skeletal related events, such as osteoporosis, loss of bone mass, and increased risk of fractures. These complications known as cancer treatment-induced bone loss (CTIBL) should be managed with bone targeting agents such as the bisphosphonates and denosumab. The latter is a monoclonal antibody against the receptor activator of nuclear factor-kB ligand (RANKL) that suppresses osteoclasts function and survival increasing bone mass. AREAS COVERED: This review will focus on the mechanisms associated with bone loss induced by cancer treatments and the most recent evidence about the use of denosumab as preventive and therapeutic strategy to protect bone health. Moreover, we will discuss several key aspects regarding the clinical practical use of denosumab to optimize the management of CTLIB in breast and prostate cancer. EXPERT OPINION: Denosumab treatment strongly prevents cancer therapies-related skeletal issues in breast and prostate cancer with a good safety profile. Adjuvant six-monthly denosumab delays the time to first fracture onset in early stage breast cancer patients with normal or altered bone mineral density (BMD). Similarly, denosumab treatment is able to prevent fractures and BMD loss in nonmetastatic prostate cancer patients.Entities:
Keywords: Cancer treatment induced bone loss (CTLIB); bone health; denosumab; osteoporosis
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Year: 2020 PMID: 32835531 DOI: 10.1080/14712598.2020.1814731
Source DB: PubMed Journal: Expert Opin Biol Ther ISSN: 1471-2598 Impact factor: 4.388