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Researchers’ 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’ 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.

A 4-week dosing schedule for&nbsp;nivolumab has been approved by the European&nbsp;Commission&nbsp;for the treatment of patients with advanced melanoma and previously treated renal cell carcinoma, Bristol-Myers Squibb (BMS), the manufacturer of the PD-1 inhibitor, has announced.