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
. 2010 Dec;36(8):615-20.
doi: 10.1016/j.ctrv.2010.04.003. Epub 2010 May 15.

Metastasis and bone loss: advancing treatment and prevention

Affiliations
Review

Metastasis and bone loss: advancing treatment and prevention

Robert E Coleman et al. Cancer Treat Rev. 2010 Dec.

Abstract

Tumor metastasis to the skeleton affects over 400,000 individuals in the United States annually, more than any other site of metastasis, including significant proportions of patients with breast, prostate, lung and other solid tumors. Research on the bone microenvironment and its role in metastasis suggests a complex role in tumor growth. Parallel preclinical and clinical investigations into the role of adjuvant bone-targeted agents in preventing metastasis and avoiding cancer therapy-induced bone loss have recently reported exciting and intriguing results. A multidisciplinary consensus conference convened to review recent progress in basic and clinical research, assess gaps in current knowledge and prioritize recommendations to advance research over the next 5 years. The program addressed three topics: advancing understanding of metastasis prevention in the context of bone pathophysiology; developing therapeutic approaches to prevent metastasis and defining strategies to prevent cancer therapy-induced bone loss. Several priorities were identified: (1) further investigate the effects of bone-targeted therapies on tumor and immune cell interactions within the bone microenvironment; (2) utilize and further develop preclinical models to study combination therapies; (3) conduct clinical studies of bone-targeted therapies with radiation and chemotherapy across a range of solid tumors; (4) develop biomarkers to identify patients most likely to benefit from bone-targeted therapies; (5) educate physicians on bone loss and fracture risk; (6) define optimal endpoints and new measures of efficacy for future clinical trials; and (7) define the optimum type, dose and schedule of adjuvant bone-targeted therapy.

PubMed Disclaimer

Conflict of interest statement

Conflict of interest statement

Brendan F. Boyce: Nothing to disclose.

Adam M. Brufsky: Consultant: Novartis; Honoraria: Novartis; Research Funding: Novartis; Royalties: Novartis.

Philippe Clézardin: Honoraria: Novartis; Research Funding: Novartis.

Robert E. ColemanConsultant: Novartis, Amgen; Research Funding: Novartis; Speakers’ Bureau: Novartis, Amgen; Expert Testimony: Novartis.

Peter I. Croucher: Research Funding: Acceleron Pharma; Speakers’ Bureau: Amgen.

Julie R. Gralow: Research Funding: Abraxane, Amgen, Bristol-Myers Squibb, Genentech, Eli Lilly, Hoffmann-La Roche, Novartis.

Theresa A. Guise: Consultant: Amgen; Research Funding: Scios; Speakers’ Bureau: Amgen, Merck, Novartis.

Peyman Hadji: Consultant: Amgen, AstraZeneca, Hoffmann-La Roche, Novartis, Pfizer; Honoraria: Amgen, AstraZeneca, Hoffmann-La Roche, Novartis, Pfizer.

Ingunn Holen: Research Funding: Novartis, Galapagos; Speakers’ Bureau: Novartis.

Allan Lipton: Expert Testimony: Novartis; Research Funding: Novartis, Monogram Biosciences, Oncogene Sciences; Speakers’ Bureau: Amgen, Novartis, Genentech, GlaxoSmithKline.

Gregory R. Mundy: Nothing to disclose.

G. David Roodman: Consultant: Acceleron, Amgen, Celgene, Novartis; Research Funding: Novartis; Speaker’s Bureau: Novartis.

Matthew R. Smith: Consultant: Amgen, GTX, Novartis.

Larry J. Suva: Nothing to disclose.

Similar articles

Cited by

References

    1. Guise TA, Yin JJ, Taylor SD, et al. Evidence for a causal role of parathyroid hormone-related protein in the pathogenesis of human breast cancer-mediated osteolysis. J Clin Invest. 1996;98:1544–9. - PMC - PubMed
    1. Engler AJ, Sen S, Sweeney HL, Discher DE. Matrix elasticity directs stem cell lineage specification. Cell. 2006;126:677–89. - PubMed
    1. Sterling JA, Oyajobi BA. The hedgegog signaling molecule Gli2 induces parathyroid hormone-related peptide expression and osteolysis in metastaic human breast cancer cells. Cancer Res. 2006;66:7548–53. - PubMed
    1. Tian E, Zhan F, Walker R, et al. The role of the Wnt-signaling antagonist DKK1 in the development of osteolytic lesions in multiple myeloma. N Engl J Med. 2003;349:2483–94. - PubMed
    1. Yaccoby S, Ling W, Zhan F, et al. Antibody-based inhibition of DKK1 suppresses tumor-induced bone resorption and multiple myeloma growth in vivo. Blood. 2007;109:2106–11. - PMC - PubMed

Publication types

MeSH terms