TY - JOUR
T1 - Molecular markers and targeted therapeutics in metastatic tumors of the spine
T2 - Changing the treatment paradigms
AU - Goodwin, C. Rory
AU - Abu-Bonsrah, Nancy
AU - Rhines, Laurence D.
AU - Verlaan, Jorrit Jan
AU - Bilsky, Mark H.
AU - Laufer, Ilya
AU - Boriani, Stefano
AU - Sciubba, Daniel M.
AU - Bettegowda, Chetan
N1 - Publisher Copyright:
© 2016 Wolters Kluwer Health, Inc. All rights reserved.
PY - 2016/10/15
Y1 - 2016/10/15
N2 - Objective. The aim of this study was to discuss the evolution of molecular signatures and the history and development of targeted therapeutics in metastatic tumor types affecting the spinal column. Summary of Background Data. Molecular characterization of metastatic spine tumors is expected to usher in a revolution in diagnostic and treatment paradigms. Molecular characterization will provide critical information that can be used for initial diagnosis, prognosticating the ideal treatment strategy, assessment of treatment efficacy, surveillance and monitoring recurrence, and predicting complications, clinical outcome, and overall survival in patients diagnosed with metastatic cancers to the spinal column. Methods. A review of the literature was performed focusing on illustrative examples of the role that molecular-based therapeutics have played in clinical outcomes for patients diagnosed with metastatic tumor types affecting the spinal column. Results. The impact of molecular therapeutics including receptor tyrosine kinases and immune checkpoint inhibitors and the ability of molecular signatures to provide prognostic information are discussed in metastatic breast cancer, lung cancer, prostate cancer, melanoma, and renal cell cancer affecting the spinal column. Conclusion. For the providers who will ultimately counsel patients diagnosed with metastases to the spinal column, molecular advancements will radically alter the management/surgical paradigms utilized. Ultimately, the translation of these molecular advancements into routine clinical care will greatly improve the quality and quantity of life for patients diagnosed with spinal malignancies and provide better overall outcomes and counseling for treating physicians.
AB - Objective. The aim of this study was to discuss the evolution of molecular signatures and the history and development of targeted therapeutics in metastatic tumor types affecting the spinal column. Summary of Background Data. Molecular characterization of metastatic spine tumors is expected to usher in a revolution in diagnostic and treatment paradigms. Molecular characterization will provide critical information that can be used for initial diagnosis, prognosticating the ideal treatment strategy, assessment of treatment efficacy, surveillance and monitoring recurrence, and predicting complications, clinical outcome, and overall survival in patients diagnosed with metastatic cancers to the spinal column. Methods. A review of the literature was performed focusing on illustrative examples of the role that molecular-based therapeutics have played in clinical outcomes for patients diagnosed with metastatic tumor types affecting the spinal column. Results. The impact of molecular therapeutics including receptor tyrosine kinases and immune checkpoint inhibitors and the ability of molecular signatures to provide prognostic information are discussed in metastatic breast cancer, lung cancer, prostate cancer, melanoma, and renal cell cancer affecting the spinal column. Conclusion. For the providers who will ultimately counsel patients diagnosed with metastases to the spinal column, molecular advancements will radically alter the management/surgical paradigms utilized. Ultimately, the translation of these molecular advancements into routine clinical care will greatly improve the quality and quantity of life for patients diagnosed with spinal malignancies and provide better overall outcomes and counseling for treating physicians.
KW - Immune checkpoint inhibitors
KW - Metastasis
KW - Molecular markers
KW - Receptor tyrosine kinase inhibitors
KW - Spine
KW - Targeted therapeutics
UR - http://www.scopus.com/inward/record.url?scp=84980373347&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84980373347&partnerID=8YFLogxK
U2 - 10.1097/BRS.0000000000001833
DO - 10.1097/BRS.0000000000001833
M3 - Review article
C2 - 27488299
AN - SCOPUS:84980373347
SN - 0362-2436
VL - 41
SP - S218-S223
JO - Spine
JF - Spine
ER -