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Nearly double the number of patients with advanced non-small cell lung cancer would be eligibile for clinical trial enrollment if a broader set of eligibility criteria proposed by the American Society of Clinical Oncology and Friends of Cancer Research was implemented, according to data presented at the 2019 ASCO Annual Meeting.

The treatment of&nbsp;<em>EGFR</em>-mutant non&ndash;small cell lung cancer has experienced significant improvements with the&nbsp;development of tyrosine kinase inhibitors, but resistance mechanisms that promote disease recurrence have tampered the runaway success of these revolutionary agents, said&nbsp;Katerina A. Politi, PhD, during the 2019 ASCO Annual Meeting. Early findings are presented for 2 novel agents aiming to potentially overcome resistance.&nbsp;

According to new findings, tumor mutational burden showed promise as a predictive biomarker for survival benefit in patients with advanced non&ndash;small cell lung cancer (NSCLC) treated with&nbsp;the PD-L1 inhibitor durvalumab (Imfinzi) as initial therapy versus chemotherapy,&nbsp;even though there was no difference seen between the 2 treatment groups in the primary analysis of the randomized trial.

Benjamin P. Levy, MD, recently discussed the treatment considerations and decisions he makes when treating patients with non&ndash;small cell lung cancer. Levy, the clinical director of medical oncology and associate professor of oncology at Johns Hopkins Sidney Kimmel Cancer Center at Sibley Memorial Hospital, revealed his treatment decisions to the group based on 2 case scenarios of patients with NSCLC that does not have a genetic driver.

The approval for&nbsp;pembrolizumab (Keytruda) has been expanded to include the&nbsp;frontline treatment of patients with stage III non&ndash;small cell lung cancer, who are ineligible for surgery or definitive chemoradiation, or metastatic NSCLC, with a PD-L1 expression level of &ge;1% and do not harbor <em>EGFR</em> or <em>ALK</em> aberrations.