AI Article Synopsis

  • The field of spinal oncology has advanced significantly, with this review analyzing clinical studies from 2000 to 2020 on primary and secondary spinal tumors registered on ClinicalTrials.gov.
  • Out of 174 studies, most were interventional and predominantly conducted in North America, focusing mainly on various treatment strategies like stereotactic radiosurgery and chemotherapy.
  • The findings reveal a greater emphasis on metastatic spinal tumors over primary tumors, indicating a need for more targeted research to improve outcomes for the rarer primary spinal neoplasms.

Article Abstract

The field of spinal oncology has substantially evolved over the past decades. This review synthesizes and appraises what was learned and what will potentially be discovered from the recently completed and ongoing clinical studies related to the treatment of primary and secondary spinal neoplasms. This scoping review included all clinical studies on the treatment of spinal neoplasms registered in the ClinicalTrials.gov website from February 2000 to December 2020. The terms "spinal cord tumor," "spinal metastasis," and "metastatic spinal cord compression" were used. Of the 174 registered clinical studies on primary spinal tumors and spinal metastasis, most of the clinical studies registered in this American registry were interventional studies led by single institutions in North America (n = 101), Europe (n = 43), Asia (n = 24), or other continents (n = 6). The registered clinical studies mainly focused on treatment strategies for spinal neoplasms (90.2%) that included investigating stereotactic radiosurgery (n = 33), radiotherapy (n = 21), chemotherapy (n = 20), and surgical technique (n = 11). Of the 69 completed studies, the results from 44 studies were published in the literature. In conclusion, this review highlights the key features of the 174 clinical studies on spinal neoplasms that were registered from 2000 to 2020. Clinical trials were heavily skewed toward the metastatic population as opposed to the primary tumors which likely reflects the rarity of the latter condition and associated challenges in undertaking prospective clinical studies in this population. This review serves to emphasize the need for a focused approach to enhancing translational research in spinal neoplasms with a particular emphasis on primary tumors.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8730766PMC
http://dx.doi.org/10.1093/neuonc/noab214DOI Listing

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