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
. 2009;19(1):47-60.
doi: 10.1615/critreveukargeneexpr.v19.i1.20.

Cancer treatment-related bone disease

Affiliations
Review

Cancer treatment-related bone disease

Sue A Brown et al. Crit Rev Eukaryot Gene Expr. 2009.

Abstract

Bone health may be impaired in many patients being treated for cancer. Primary tumors that reside in or form metastases to bone can result in compromised skeletal integrity. It has also been increasingly recognized that patients undergoing therapies for treatment of cancer are at higher risk of bone loss. These include androgen-deprivation therapy for prostate cancer and aromatase inhibitor therapy for breast cancer, among others. Hypogonadism induced by many of these cancer treatments results in bone loss and increases the risk of osteoporosis and fractures. Progress has been made in identifying the role of oral and intravenous bisphosphonates to prevent bone loss in these patients. This review discusses bone loss associated with cancer treatments, with a focus on breast cancer, prostate cancer, and survivors of childhood malignancies.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Bone mineral density loss with cancer therapies. Cancer treatment induced bone loss after 1 year often exceeds that seen in normal men and postmenopausal women. BMD=bone mineral density; AI=aromatase inhibitor. Data from Hirbe et al. (1), adapted and reprinted with permission from American Association for Cancer Research, Inc.

References

    1. Hirbe A, Morgan EA, Uluckan O, Weilbaecher K. Skeletal complications of breast cancer therapies. Clin Cancer Res. 2006 Oct 15;12(20 Pt 2):6309s–14s. - PMC - PubMed
    1. Pfeilschifter J, Diel IJ. Osteoporosis due to cancer treatment: pathogenesis and management. J Clin Oncol. 2000 Apr;18(7):1570–93. - PubMed
    1. Feng JQ, Ward LM, Liu S, Lu Y, Xie Y, Yuan B, et al. Loss of DMP1 causes rickets and osteomalacia and identifies a role for osteocytes in mineral metabolism. Nat Genet. 2006 Nov;38(11):1310–5. - PMC - PubMed
    1. Lee JS, Lacroix AZ, Wu L, Cauley JA, Jackson RD, Kooperberg C, et al. Associations of serum sex hormone-binding globulin and sex hormone concentrations with hip fracture risk in postmenopausal women. J Clin Endocrinol Metab. 2008 Mar 11; - PMC - PubMed
    1. Meier C, Nguyen TV, Handelsman DJ, Schindler C, Kushnir MM, Rockwood AL, et al. Endogenous sex hormones and incident fracture risk in older men: the Dubbo Osteoporosis Epidemiology Study. Arch Intern Med. 2008 Jan 14;168(1):47–54. - PubMed

Publication types