Updated phase 2 data showed a 60% ORR and 86% CNS ORR with frontline silevertinib in non-classical EGFR-mutant NSCLC; FDA discussion supported a phase 3 trial in 2027.
|Videos|September 2, 2014
Selecting Patients for Treatment with CO-1686
Andrew R. Allen, BM, BCh, MA, MRCP, PhD, Executive Vice President of Clinical and Pre-Clinical Development, Chief Medical Officer, Co-Founder, Clovis Oncology, discusses how patients are selected for treatment with CO-1686.
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Andrew R. Allen, BM, BCh, MA, MRCP, PhD, Executive Vice President of Clinical and Pre-Clinical Development, Chief Medical Officer, Co-Founder, Clovis Oncology, discusses how patients are selected for treatment with CO-1686.
Clinical Pearls:
- The vast majority of patients with newly diagnosed lung cancer have an analysis of their EGFR genes looking for the activating mutations.
- This is done on tissue using PCR testing.
- Clovis Oncology uses a tissue-based T790M detection test for the identification of appropriate patients in clinical trials involving CO-1686.
- While there is a lot of interest in plasma as a way of detecting mutations in patients, it is not yet replacing tissue-based testing.​
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