Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2018 Feb;102(2):251-264.
doi: 10.1007/s00223-017-0369-x. Epub 2018 Jan 20.

Cancer Treatment and Bone Health

Affiliations
Review

Cancer Treatment and Bone Health

Catherine Handforth et al. Calcif Tissue Int. 2018 Feb.

Abstract

Considerable advances in oncology over recent decades have led to improved survival, while raising concerns about long-term consequences of anticancer treatments. In patients with breast or prostate malignancies, bone health is a major issue due to the high risk of bone metastases and the frequent prolonged use of hormone therapies that alter physiological bone turnover, leading to increased fracture risk. Thus, the onset of cancer treatment-induced bone loss (CTIBL) should be considered by clinicians and recent guidelines should be routinely applied to these patients. In particular, baseline and periodic follow-up evaluations of bone health parameters enable the identification of patients at high risk of osteoporosis and fractures, which can be prevented by the use of bone-targeting agents (BTAs), calcium and vitamin D supplementation and modifications of lifestyle. This review will focus upon the pathophysiology of breast and prostate cancer treatment-induced bone loss and the most recent evidence about effective preventive and therapeutic strategies.

Keywords: BMD; Breast cancer; Cancer treatment; Osteoporosis; Prostate cancer.

PubMed Disclaimer

Conflict of interest statement

REC—research funding from Amgen. JB—consultancy/Advisory Board Membership for Amgen and Novartis. CH and SD—no conflicts of interest.

Figures

Fig. 1
Fig. 1
Algorithm for the assessment and management of cancer treatment-induced bone loss [70]. a Aromatase inhibitors and ovarian suppression therapy/oophorectomy for BC and androgen deprivation therapy for prostate cancer. b If patients experience an annual decrease in BMD of ≥ 10% (or ≥ 4–5% in patients who were osteopenic at baseline) using the same DXA machine, secondary causes of bone loss such as vitamin D deficiency should be evaluated and antiresorptive therapy initiated. Use lowest t score from spine and hip. c Six monthly intravenous zoledronate, weekly oral alendronate or risedronate or monthly oral ibandronate acceptable. d Denosumab may be a potential treatment option in some patients. e Although osteonecrosis of the jaw is a very rare event with bone protection doses of antiresorptives, regular dental care and attention to oral health are advisable. BMD bone mineral density, BMI body mass index, DXA dual-energy X-ray absorptiometry

References

    1. CRUK (2016) Cancer research UK breast cancer statistics. http://www.cancerresearchuk.org/health-professional/cancer-statistics/st.... Accessed 11 Feb 2017
    1. CRUK (2013) Cancer statistics http://www.cancerresearchuk.org/health-professional/cancer-statistics/st.... Accessed 15 Apr 2016
    1. Carnevale V, Romagnoli E, Cipriani C, Del Fiacco R, Piemonte S, Pepe J, Scillitani A, Minisola S. Sex hormones and bone health in males. Arch Biochem Biophys. 2010;503(1):110–117. doi: 10.1016/j.abb.2010.07.001. - DOI - PubMed
    1. Wilson JD. The role of 5α reductase in steroid hormone physiology. Reprod Fertil Dev. 2001;13(7–8):673–678. doi: 10.1071/RD01074. - DOI - PubMed
    1. Clarke BL, Khosla S. Androgens and Bone. Steroids. 2009;74(3):296–305. doi: 10.1016/j.steroids.2008.10.003. - DOI - PMC - PubMed

Publication types

MeSH terms