A Phase II trial of alternating osimertinib and gefitinib therapy in advanced EGFR-T790M positive non-small cell lung cancer: OSCILLATE

Author:

Tan Lavinia,Brown ChrisORCID,Mersiades Antony,Lee Chee Khoon,John ThomasORCID,Kao Steven,Newnham Genni,O’Byrne Kenneth,Parakh Sagun,Bray Victoria,Jasas Kevin,Yip Sonia,Wong Stephen Q.,Ftouni Sarah,Guinto Jerick,Chandrashekar Sushma,Clarke Stephen,Pavlakis Nick,Stockler Martin R.,Dawson Sarah-JaneORCID,Solomon Benjamin J.ORCID

Abstract

AbstractIn this phase II, single arm trial (ACTRN12617000720314), we investigate if alternating osimertinib and gefitinib would delay the development of resistance to osimertinib in advanced, non-small cell lung cancer (NSCLC) with the epidermal growth factor receptor (EGFR) T790M mutation (n = 47) by modulating selective pressure on resistant clones. The primary endpoint is progression free-survival (PFS) rate at 12 months, and secondary endpoints include: feasibility of alternating therapy, overall response rate (ORR), overall survival (OS), and safety. The 12-month PFS rate is 38% (95% CI 27.5–55), not meeting the pre-specified primary endpoint. Serial circulating tumor DNA (ctDNA) analysis reveals decrease and clearance of the original activating EGFR and EGFR-T790M mutations which are prognostic of clinical outcomes. In 73% of participants, loss of T790M ctDNA is observed at progression and no participants have evidence of the EGFR C797S resistance mutation following the alternating regimen. These findings highlight the challenges of treatment strategies designed to modulate clonal evolution and the clinical importance of resistance mechanisms beyond suppression of selected genetic mutations in driving therapeutic escape to highly potent targeted therapies.

Funder

Department of Health | National Health and Medical Research Council

AstraZeneca Australia

Publisher

Springer Science and Business Media LLC

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