EGFR+ Lung Cancer

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Bristol-Myers Squibb has announced its decision to withdraw a supplemental biologics license application currently with the FDA seeking frontline approval for the combination of nivolumab and ipilimumab for patients with advanced non–small cell lung cancer with tumor mutational burden ≥10 mutations per megabase.

Both overall survival and progression-free survival were improved in patients with <em>EGFR</em>-mutant nonsquamous cell lung cancer who were treated with the combination of atezolizumab, bevacizumab, and chemotherapy compared with bevacizumab plus chemotherapy, according to an exploratory analysis of the IMpower150 study.

A supplemental biologics license application submitted to the FDA for&nbsp;atezolizumab, carboplatin, and nab-paclitaxel has been accepted. The application, based on findings from the&nbsp;phase III IMpower130 trial, is seeking the agent&#39;s approval for&nbsp;patients with metastatic nonsquamous non&ndash;small cell lung cancer.

Increasing clinical relevance of less common gene signatures and alterations is leading to a benefit from broad-panel next-generation sequencing testing for patients with metastatic non&ndash;small cell lung cancer, according to an expert at Memorial Sloan Kettering Cancer Center.