The genotype-directed use of EGFR TKIs in EGFR-mutant lung cancer patients has fundamentally changed the face of the disease with improved response to therapy, preserved quality of life, and prolonged progression-free and overall survival. However, tumors that initially respond acquire resistance after about 1 year. In 50-60% of cases, resistance is mediated by the T790M resistance mutation in the gatekeeper location. However, we now appreciate that it may be overly simplistic to categorize cancers in a binary fashion such as T790M positive or negative. We have observed that within an individual patient there exist intra- tumoral and inter-tumoral heterogeneity with respect to T790M. Importantly, novel T790M-specific 3rd- generation EGFR inhibitors are currently entering the clinic and have shown significant activity in phase I trials for patients whose tumors harbor T790M. We have also learned that a subset of T790M positive cancers are intrinsically resistant to T790M inhibitors because they are no longer solely reliant on EGFR signaling for their viability. Thus, there is an increasing urgency to understand T790M heterogeneity, intrinsic resistance and their implications on patient response to these new therapies. In this proposal, we will tackle two aspects limiting the efficacy to 3rd generation EGFR TKIs; clonal heterogeneity and intrinsic lack of sensitivity. We will comprehensively explore clonal T790M heterogeneity in EGFR-mutant cancers with acquired resistance to the initial EGFR TKIs, and expand on our Preliminary Data suggesting that the amount of heterogeneity impacts response to 3rd-generation EGFR inhibitors. Utilizing cell lines derived directly from patient biopsies, we will also design and test therapeutic strategies to improve treatment outcomes in tumors that are inherently resistant to 3rd-generation TKIs. This study should lay the groundwork for newer diagnostic and treatment paradigms that assess, combat and overcome the complexities of targeted therapy resistance so patients can enjoy long-term remissions or even cures.
Specific Aim 1 : Define the intra- and inter-tumoral heterogeneity of T790M clones in cancers with acquired resistance to EGFR TKIs Specific Aim 2: Determine if T790M heterogeneity predicts responsiveness to 3rd generation EGFR inhibitors.
Specific Aim 3 : Identify therapeutic strategies for T790M cancers with intrinsic resistance to 3rd generation EGFR inhibitors.

Public Health Relevance

The tyrosine kinase inhibitors erlotinib and gefitinib are the standard of care for patients with EGFR mutant NSCLC, but cancers invariably develop resistance, often through the acquisition of a T790M gatekeeper mutation. Next generation inhibitors have been developed that can specifically inhibit EGFR with T790M and have shown significant promise early on in the clinic, but recent evidence has revealed that clones with distinct resistance mechanisms can present within an individual tumor (biopsy) and across distinct metastatic sites, potentially limiting efficacy. In this proposal, we aim to utilize novel technologies to better define and characterize the heterogeneity that exists in resistant cancers, to determine the relationship between heterogeneity and response to next generation TKIs, and to develop combination therapeutic approaches to enhance the efficacy of these drugs in T790M cancers that fail to respond to 3rd generation EGFR inhibitors.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
2R01CA137008-06
Application #
8887518
Study Section
Basic Mechanisms of Cancer Therapeutics Study Section (BMCT)
Program Officer
Forry, Suzanne L
Project Start
2009-03-01
Project End
2020-03-31
Budget Start
2015-04-01
Budget End
2016-03-31
Support Year
6
Fiscal Year
2015
Total Cost
$406,220
Indirect Cost
$168,720
Name
Massachusetts General Hospital
Department
Type
DUNS #
073130411
City
Boston
State
MA
Country
United States
Zip Code
02114
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