An example of this approach is my laboratory's work with AZD6244, a MEK inhibitor. My laboratory demonstrated the therapeutic potential of MEK inhibition as a radiation sensitizer in several cancers both in vitro and in vivo,(12) evaluated the impact of concurrent chemotherapy on the radiosensitizing effect of MEK inhibition,(13) identified biomarkers that may predict efficacy of this approach, and highlighted the mechanisms of radiation sensitization when this pathway is targeted.(12-14) This work culminated in the initiation of a CTEP sponsored Phase I trial at the NCI investigating MEK inhibition combined with the current standard chemoradiotherapy in the neoadjuvant setting in patients with locally advanced rectal cancer. There are currently three open and two completed Phase I clinical trials evaluating MEK inhibition combined with radiation and chemotherapy for the treatment of localized cancers. We have recently identified additional compounds that show preliminary efficacy in vitro as radiation sensitizers. The approach we have used in the past to select agents for study has been effective in identifying radiation sensitizers. However, this approach is evolving as we collect tumor tissue and clinical outcomes data from prostate cancer patients on my protocol, 13-C-0119. This clinical trial will allow us to evaluate multiple biologic, clinical, and radiographic predictors of local failure in patients treated with radiotherapy for localized prostate cancer. Patients enrolled in this study undergo a pretreatment multiparametric MRI and MRI-guided research biopsy of all tumors within their prostate. Following radiation therapy, patients with a rising PSA who meet biochemical failure criteria undergo repeat multiparametric MRI of the prostate and repeat MRI-guided research biopsy of persistent tumor. The molecular characteristics of tumor are analyzed to evaluate for predictors of failure and to study tumor evolution after radiation. Data from the tissue studies described above will be mined to generate a list of candidate pathway responsible for radiation resistance in prostate cancer. These data will inform laboratory studies aimed at determining the importance of these pathways in radiation response.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Investigator-Initiated Intramural Research Projects (ZIA)
Project #
1ZIABC011552-06
Application #
10014725
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
6
Fiscal Year
2019
Total Cost
Indirect Cost
Name
National Cancer Institute Division of Basic Sciences
Department
Type
DUNS #
City
State
Country
Zip Code
Valle, Luca F; Greer, Matthew D; Shih, Joanna H et al. (2018) Multiparametric MRI for the detection of local recurrence of prostate cancer in the setting of biochemical recurrence after low dose rate brachytherapy. Diagn Interv Radiol 24:46-53
Liu, Qi; Gheorghiu, Liliana; Drumm, Michael et al. (2018) PARP-1 inhibition with or without ionizing radiation confers reactive oxygen species-mediated cytotoxicity preferentially to cancer cells with mutant TP53. Oncogene 37:2793-2805
Reed, Aaron; Valle, Luca F; Shankavaram, Uma et al. (2017) Effect of Prostate Magnetic Resonance Imaging/Ultrasound Fusion-guided Biopsy on Radiation Treatment Recommendations. Int J Radiat Oncol Biol Phys 97:947-951
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Valle, Luca; Thomas, Joel; Kim, Chul et al. (2017) Hepatoid adenocarcinoma of the lung metastasizing to the tonsil. Mol Clin Oncol 6:705-707
Citrin, Deborah E (2016) Short-Term Screening Assays for the Identification of Therapeutics for Cancer. Cancer Res 76:3443-5
Premo, Christopher; Apolo, Andrea B; Agarwal, Piyush K et al. (2015) Trimodality therapy in bladder cancer: who, what, and when? Urol Clin North Am 42:169-80, vii
Citrin, Deborah E; Mitchell, James B (2014) Altering the response to radiation: sensitizers and protectors. Semin Oncol 41:848-59
Park, Jong Chul; Citrin, Deborah E; Agarwal, Piyush K et al. (2014) Multimodal management of muscle-invasive bladder cancer. Curr Probl Cancer 38:80-108