Dr. West on the Use of Nivolumab/Ipilimumab in Metastatic NSCLC
Howard (Jack) West, MD, discusses the use of nivolumab in combination with ipilimumab in metastatic non–small cell lung cancer.
EP: 1.Dr. Giaccone on Treatment Options in NSCLC
EP: 2.Dr. Rizvi on Biomarkers of Response to Immunotherapy in NSCLC
EP: 3.Dr. West on the Use of Nivolumab/Ipilimumab in Metastatic NSCLC
EP: 4.Dr. Gandara on the Benefit of Nivolumab/Ipilimumab Plus Chemo in Metastatic NSCLC
EP: 5.Dr. Rizvi on the Implications of the CheckMate-227 Trial With Nivolumab/Ipilimumab in NSCLC
EP: 6.Dr. Wozniak on Optimizing the Use of Immunotherapy in NSCLC
EP: 7.Dr. Raez on the Impact of PD-L1 Status on Immunotherapy Outcomes in NSCLC
EP: 8.Dr. Garon on Immunotherapy Treatment Considerations in NSCLC
EP: 9.The Evolving Role of Immunotherapy in Metastatic Non–Small Cell Lung Cancer
Howard (Jack) West, MD, executive director of Employer Strategy and associate clinical professor of the Department of Medical Oncology & Therapeutics Research, discusses the use of nivolumab (Opdivo) in combination with ipilimumab (Yervoy) in metastatic non–small cell lung cancer (NSCLC).
The combination has been utilized in this disease for several years; however, within the past 18 months, nivolumab/ipilimumab has demonstrated an overall survival benefit in this patient population, according to West. This benefit extends to patients who have PD-L1 positivity and those who do not, as well as in those with squamous or nonsquamous histology, West adds.
The phase 3 CheckMate-227 trial led to the May 2020 FDA approval of nivolumab/ipilimumab in the treatment of patients with metastatic NSCLC without EGFR or ALK genomic tumor aberrations, and whose tumors express a PD-L1 level of 1% or greater. In this trial, the comparator was single-agent chemotherapy, an older standard of care that has since been replaced, says West. In some ways, this is a lateral progression due to pembrolizumab (Keytruda) having shown superiority to single-agent chemotherapy in the phase 3 KEYNOTE-024 and KEYNOTE-042 trials, in which the agent showed benefit in the PD-L1–high population, West concludes.
