• Spine · Aug 2016

    The Risk of Cancer with the Use of Recombinant Human Bone Morphogenetic Protein in Spine Fusion.

    • Joseph R Dettori, Jens R Chapman, John G DeVine, Robert A McGuire, Daniel C Norvell, and Noel S Weiss.
    • *Department of Evidence Based Medicine, Spectrum Research, Inc., Tacoma, WA†Swedish Neuroscience Institute, Swedish Medical Center, Jefferson Tower, Seattle, WA‡Department of Orthopedics, Spine Surgery Service, Georgia Regents University, Augusta, GA§Department of Orthopedic Surgery and Rehabilitation, University of Mississippi Medical Center, Jackson, MS¶Department of Epidemiology, University of Washington, Seattle, WA.
    • Spine. 2016 Aug 15; 41 (16): 1317-24.

    Study DesignRetrospective cohort study using the Washington State Comprehensive Hospital Abstract Reporting System, the Washington State Cancer Registry, and Washington State death certificates.ObjectiveTo study the possible association between recombinant human bone morphogenetic protein (rhBMP) and cancer risk.Summary Of Background DataThe use of rhBMP in spine fusion surgery remains controversial with respect to its possible role in tumorigenesis.MethodsWe compared adults who underwent spine fusion for degenerative disease with and without rhBMP between 2002 and 2010. Patients were matched on the basis of age, sex, and year of treatment. We excluded patients with a diagnosis of cancer before or at the index procedure. The primary outcome was the first diagnosis of cancer as identified in the records of the cancer registry.ResultsWe included 16,914 patients who had spine fusion, of whom 4246 received rhBMP. During the study period, 449 patients received a diagnosis of cancer: 117 (2.76% of 4246) in the rhBMP group and 332 (2.62% of 12 668) in the no rhBMP group. The incidence rate was similar between the rhBMP and no rhBMP 9.5 and 9.0 per 1000 person years, respectively (hazard ratio, 1.06; 95% confidence interval, 0.86-1.30). There were no differences in the rate of cancer between the two groups in subgroups defined on the basis of site of fusion or surgical method.ConclusionThere was no increase in overall cancer incidence among those receiving rhBMP. An important limitation of this and other studies of rhBMP and cancer that have been conducted to date is their relatively limited duration of follow-up. The examination of cancer incidence following rhBMP administration must continue beyond just the first several years to adequately assess the potential of rhBMP to influence the occurrence of one or more types of malignancy.Level Of Evidence3.

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