TY - JOUR
T1 - Radiogenomics predicting tumor responses to radiotherapy in lung cancer
AU - Das, Amit K.
AU - Bell, Marcus H.
AU - Nirodi, Chaitanya S.
AU - Story, Michael D.
AU - Minna, John D.
N1 - Funding Information:
Supported by NIH/NCI the University of Texas SPORE in Lung Cancer 5P50 CA 70907 (Dr John D. Minna) and NASA/DOE NASA Specialized Center of Research (NSCOR) NNJ05HD36G/DEAI0205ER64068 (Dr John D. Minna).
PY - 2010/7
Y1 - 2010/7
N2 - The recently developed ability to interrogate genome-wide data arrays has provided invaluable insights into the molecular pathogenesis of lung cancer. These data have also provided information for developing targeted therapy in lung cancer patients based on the identification of cancer-specific vulnerabilities and set the stage for molecular biomarkers that provide information on clinical outcome and response to treatment. In addition, there are now large panels of lung cancer cell lines, both non-small-cell lung cancer and small-cell lung cancer, that have distinct chemotherapy and radiation response phenotypes. We anticipate that the integration of molecular data with therapy response data will allow for the generation of biomarker signatures that predict response to therapy. These signatures will need to be validated in clinical studies, at first retrospective analyses and then prospective clinical trials, to show that the use of these biomarkers can aid in predicting patient outcomes (eg, in the case of radiation therapy for local control and survival). This review highlights recent advances in molecular profiling of tumor responses to radiotherapy and identifies challenges and opportunities in developing molecular biomarker signatures for predicting radiation response for individual patients with lung cancer.
AB - The recently developed ability to interrogate genome-wide data arrays has provided invaluable insights into the molecular pathogenesis of lung cancer. These data have also provided information for developing targeted therapy in lung cancer patients based on the identification of cancer-specific vulnerabilities and set the stage for molecular biomarkers that provide information on clinical outcome and response to treatment. In addition, there are now large panels of lung cancer cell lines, both non-small-cell lung cancer and small-cell lung cancer, that have distinct chemotherapy and radiation response phenotypes. We anticipate that the integration of molecular data with therapy response data will allow for the generation of biomarker signatures that predict response to therapy. These signatures will need to be validated in clinical studies, at first retrospective analyses and then prospective clinical trials, to show that the use of these biomarkers can aid in predicting patient outcomes (eg, in the case of radiation therapy for local control and survival). This review highlights recent advances in molecular profiling of tumor responses to radiotherapy and identifies challenges and opportunities in developing molecular biomarker signatures for predicting radiation response for individual patients with lung cancer.
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U2 - 10.1016/j.semradonc.2010.01.002
DO - 10.1016/j.semradonc.2010.01.002
M3 - Review article
C2 - 20685577
AN - SCOPUS:77954853984
SN - 1053-4296
VL - 20
SP - 149
EP - 155
JO - Seminars in Radiation Oncology
JF - Seminars in Radiation Oncology
IS - 3
ER -