An evidence-based medicine model for rare and often neglected neoplastic conditions

Author:

Fisher Charles G.1,Goldschlager Tony12,Boriani Stefano3,Varga Peter Paul4,Rhines Laurence D.5,Fehlings Michael G.6,Luzzati Alessandro7,Dekutoski Mark B.8,Reynolds Jeremy J.9,Chou Dean10,Berven Sigurd H.11,Williams Richard P.12,Quraishi Nasir A.13,Bettegowda Chetan14,Gokaslan Ziya L.14

Affiliation:

1. Division of Spine, Department of Orthopaedics, University of British Columbia and Vancouver CoastalHealth, Vancouver, British Columbia;

2. Monash Institute of Medical Research, Monash University, Clayton, Victoria, Australia; and

3. Unit of Oncologic and Degenerative Spine Surgery, Rizzoli Institute, Bologna;

4. National Center for Spinal Disorders and Buda Health Center, Budapest, Hungary;

5. Department of Neurosurgery, MD Anderson Cancer Center, The University of Texas, Houston, Texas;

6. Division of Neurosurgery, Department of Surgery, University of Toronto and Toronto Western Hospital, Toronto, Ontario, Canada;

7. Oncologia Ortopedica e Ricostruttiva del Rachide, Istituto Ortopedico Galeazzi, Milano, Italy;

8. The CORE Institute, Phoenix, Arizona;

9. Spinal Division, Oxford University Hospitals NHS Trust, Oxford;

10. Departments of Neurological Surgery and

11. Orthopaedic Surgery, University of California, San Francisco, California;

12. Department of Orthopaedics, Princess Alexandra Hospital, Brisbane, Queensland;

13. Center for Spine Studies and Surgery, Queens Medical Centre, Nottingham University Hospitals NHS Trust, Nottingham, United Kingdom;

14. Department of Neurosurgery, Johns Hopkins University School of Medicine, Baltimore, Maryland

Abstract

Object The National Institutes of Health recommends strategies to obtain evidence for the treatment of rare conditions such as primary tumors of the spine (PTSs). These tumors have a low incidence and are pathologically heterogeneous, and treatment approaches are diverse. Appropriate evidence-based care is imperative. Failure to follow validated oncological principles may lead to unnecessary mortality and profound morbidity. This paper outlines a scientific model that provides significant evidence guiding the treatment of PTSs. Methods A four-stage approach was used: 1) planning: data from large-volume centers were reviewed to provide insight; 2) recruitment: centers were enrolled and provided the necessary infrastructure; 3) retrospective stage: existing medical records were reviewed and completed with survival data; and 4) prospective stage: prospective data collection has been implemented. The AOSpine Knowledge Forum Tumor designed six modules: demographic, clinical, diagnostic, therapeutic, local recurrence, survival, and perioperative morbidity data fields and provided funding. Results It took 18 months to implement Stages 1–3, while Stage 4 is ongoing. A total of 1495 tumor cases were captured and diagnosed as one of 18 PTS histotypes. In addition, a PTS biobank network has been created to link clinical data with tumor pathology and molecular analysis. Conclusions This scientific model has not only aggregated a large amount of PTS data, but has also established an international collaborative network of spine oncology centers. Access to large volumes of data will generate further research to guide and enhance PTS clinical management. This model could be applied to other rare neoplastic conditions. Clinical trial registration no.: NCT01643174 (ClinicalTrials.gov).

Publisher

Journal of Neurosurgery Publishing Group (JNSPG)

Subject

General Medicine

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