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      Incidence of bone metastases in patients with solid tumors: analysis of oncology electronic medical records in the United States

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          Abstract

          Background

          Bone metastases commonly occur in conjunction with solid tumors, and are associated with serious bone complications. Population-based estimates of bone metastasis incidence are limited, often based on autopsy data, and may not reflect current treatment patterns.

          Methods

          Electronic medical records (OSCER, Oncology Services Comprehensive Electronic Records, 569,000 patients, 52 US cancer centers) were used to identify patients ≥18 years with a solid tumor diagnosis recorded between 1/1/2004 and 12/31/2013, excluding patients with hematologic tumors or multiple primaries. Each patient’s index date was set to the date of his or her first solid tumor diagnosis in the selection period. Kaplan-Meier analyses were used to quantify the cumulative incidence of bone metastasis with follow-up for each patient from the index date to the earliest of the following events: last clinic visit in the OSCER database, occurrence of a new primary tumor or bone metastasis, end of study (12/31/2014). Incidence estimates and associated 95% confidence intervals (CI) are provided for up to 10 years of follow-up for all tumor types combined and stratified by tumor type and stage at diagnosis.

          Results

          Among 382,733 study patients (mean age 64 years; mean follow-up 940 days), breast (36%), lung (16), and colorectal (12%) tumors were most common. Mean time to bone metastasis was 400 days (1.1 years). Cumulative incidence of bone metastasis was 2.9% (2.9–3.0) at 30 days, 4.8% (4.7–4.8) at one year, 5.6% (5.5–5.6) at two years, 6.9% (6.8–7.0) at five years, and 8.4% (8.3–8.5) at ten years. Incidence varied substantially by tumor type with prostate cancer patients at highest risk (18% – 29%) followed by lung, renal or breast cancer. Cumulative incidence of bone metastasis increased by stage at diagnosis, with markedly higher incidence among patients diagnosed at Stage IV of whom11% had bone metastases diagnosed within 30 days.

          Conclusions

          These estimates of bone metastasis incidence represent the experience of a population with longer follow-up than previously published, and represent experience in the recent treatment landscape. Underestimation is possible given reliance on coded diagnoses but the clinical detail available in electronic medical records contributes to the accuracy of these estimates.

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          Most cited references16

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          Bone metastasis, skeletal-related events, and mortality in lung cancer patients: a Danish population-based cohort study.

          To estimate the incidence rate of bone metastasis and subsequent skeletal-related events (SREs) (radiation to bone, spinal cord compression, fracture, and surgery to bone) in lung cancer patients and to quantify their impact on mortality.
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            Metastasis and bone loss: advancing treatment and prevention.

            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. Copyright © 2010 Elsevier Ltd. All rights reserved.
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              Skeletal Fractures Negatively Correlate With Overall Survival in Men With Prostate Cancer

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                Author and article information

                Contributors
                rohinih@amgen.com
                sallyw@amgen.com
                areich@us.imshealth.com
                m.pirolli@us.imshealth.com
                aliede@amgen.com
                GLYMAN@FHCRC.ORG
                Journal
                BMC Cancer
                BMC Cancer
                BMC Cancer
                BioMed Central (London )
                1471-2407
                6 January 2018
                6 January 2018
                2018
                : 18
                : 44
                Affiliations
                [1 ]ISNI 0000 0001 0657 5612, GRID grid.417886.4, Amgen, Inc., ; One Amgen Center Drive, Thousand Oaks, CA 91320 USA
                [2 ]Wade Outcomes Research and Consulting, 358 South 700 East, Suite B432, Salt Lake City, UT 84102 USA
                [3 ]IMS Health, 1 IMS Drive, Plymouth Meeting, PA 19462 USA
                [4 ]ISNI 0000000122986657, GRID grid.34477.33, Fred Hutchinson Cancer Research Center, , University of Washington School of Medicine, ; 1100 Fairview Ave N, Seattle, Washington, 98109 USA
                [5 ]ISNI 0000 0001 0657 5612, GRID grid.417886.4, Amgen, Inc., ; 1120 Veterans Blvd, South San Francisco, CA 94114 USA
                Article
                3922
                10.1186/s12885-017-3922-0
                5756362
                29306325
                bd26ab57-52b0-463b-a7d4-f8a913f0c3fc
                © The Author(s). 2018

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 29 June 2016
                : 14 December 2017
                Funding
                Funded by: Amgen Inc.
                Categories
                Research Article
                Custom metadata
                © The Author(s) 2018

                Oncology & Radiotherapy
                solid tumor,bone metastasis,incidence,epidemiology
                Oncology & Radiotherapy
                solid tumor, bone metastasis, incidence, epidemiology

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