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Several biomarkers are beginning to emerge for immunotherapy in non&ndash;small cell lung cancer, and the collection of these markers, when used together, could further help to predict which patients are likely to respond to these therapies alone or in combination, according to a presentation by Giorgio Scagliotti, MD, PhD, at the <em>19th Annual</em> International Lung Cancer Congress.

Immunotherapy may provide an opportunity to change the treatment paradigm of small cell lung cancer as new clinical trials report out in the next year, says&nbsp;Anne Chiang, MD, PhD.&nbsp;Recent results with immunotherapy agents in the second-line setting have already influenced guidelines.

A&nbsp;supplemental biologics license application has been accepted by the FDA seeking approval for&nbsp;the combination of nivolumab plus ipilimumab for the frontline treatment of patients with advanced non&ndash;small cell lung cancer with tumor mutational burden&nbsp; &ge;10 mutations per megabase, according to Bristol-Myers Squibb, the manufacturer of both immune checkpoint inhibitors.

Researchers&rsquo; understanding of why patients with cancer do or do not respond to treatment with immune checkpoint inhibition is constantly evolving, with new developments in innate and adaptive immunity, the tumor microenvironment, and more changing the way that immunotherapy is viewed and used. Many researchers are now pointing to the effect that gut microbiota have on patients&rsquo;&nbsp;response to checkpoint inhibitors and its implications for the treatment of patients receiving immunotherapy.

Editori-in-Chief of <em>Targeted Therapies in Oncology </em>discusses the importance of KEYNOTE-189 which investigated whether the best frontline treatment for any patient is chemotherapy, immunotherapy, or a combination of the 2. Data from the IMpower150 and CheckMate 227 also investigate this question in various patient populations.