Press Release
Jan 12, 2021
Chris Martin CMartin@DavidJamesGroup.com | 630-670-2745
Research presented today at the International Association for the Study of Lung Cancer’s World Conference on Lung Cancer
Singapore (Embargoed January 30, 2021) — Adding ipilimumab to pembrolizumab does not improve efficacy and is associated with greater toxicity than pembrolizumab alone as first-line therapy for metastatic non-small cell lung cancer (NSCLC) for patients with a PD-L1 tumor proportion score of greater than or equal to 50% and no targetable EGFR or ALK aberrations, according to research presented today at the International Association for the Study of Lung Cancer’s World Conference on Lung Cancer.
The research was presented by Dr. Michael Boyer, clinical professor of medicine at the Chris O’Brien Lifehouse and the Central Clinical School of the University of Sydney, Sydney, Australia.
Previously, the KEYNOTE-024 study showed that pembrolizumab monotherapy significantly improved survival versus platinum-doublet chemotherapy for patients with metastatic NSCLC, a PD-L1 TPS greater than or equal to 50%, and no targetable EGFR or ALK aberrations.
Boyer and his research group, which consisted of centers in Europe, Asia, and North America, conducted the randomized, double-blind, phase III KEYNOTE-598 study (NCT03302234) to determine whether adding ipilimumab to pembrolizumab improved efficacy over pembrolizumab alone in this population.
The trial enrolled 568 participants — 284 received a combination of pembrolizumab and ipilimumab and 284 were randomly assigned to receive pembrolizumab and placebo.
Patients were randomly assigned 1:1 to ipilimumab at 1 mg/kg every six weeks or to saline placebo for up to 18 cycles. Patients in both arms received 200 mg of pembrolizumab every three weeks for up to 35 cycles. Random assignment was stratified by European Cooperative Oncology Group score of (0 vs 1), region (East Asia vs not East Asia), and histology (squamous vs nonsquamous). Treatment differences in the primary endpoints of overall survival and progress-free survival were assessed by the stratified log-rank test in the intent-to-treat population.
The protocol-specified first interim analysis (IA1) was planned to occur when approximately 255 deaths occurred and approximately 12 months had passed since the last participant was randomly assigned. Nonbinding futility criteria at IA1 were differences in the restricted mean survival time between ipilimumab/pembrolizumab and placebo/pembrolizumab of less than or equal to 0.2 at the maximum observation time and less than or equal to 0.1 at 24 months of follow-up.
With 272 deaths, median overall survival was 21.4 months for patients who received ipilimumab/pembrolizumab compared to 21.9 months for placebo/pembrolizumab (HR, 1.08 ;95% CI: 0.85-1.37; p = 0.74). Restricted mean survival time differences were –0.56 at the maximum observation time and –0.52 at 24 months, which met the futility criteria, according to Dr. Boyer.
With 372 events, median progression-free survival was 8.2 months for the ipilimumab/pembrolizumab group compared with 8.4 months for placebo/pembrolizumab (HR, 1.06; 95% CI: 0.86-1.30; p = 0.72). The objective response rate was 45.4% in both arms; median duration of response was 16.1 months for the ipilimumab/pembrolizumab group vs 17.3 months for placebo/pembrolizumab. Treatment-related adverse events occurred in 76.2% of patients in the ipilimumab/pembrolizumab group versus 68.3% for the placebo group.
Dr. Boyer reported that based on the observed efficacy and safety, the external data monitoring committee recommended that the study be stopped due to futility and that participants discontinue both ipilimumab and placebo.
“As a consequence of the results of this study, monotherapy with pembrolizumab remains a standard of care for this population of patients. Despite the benefits of this type of treatment, almost 50% of these patients die of their disease within two years, so future research will focus on other ways to improve outcomes,” he reported.
“Although this is a negative study, it helps in defining the optimal chemotherapy-sparing treatment in the subgroup of patients with advanced-stage NSCLC and with tumors expressing high levels of PDL-1 as assessed by immunohistochemistry,” said Dr. Giorgio Scagliotti, interim IASLC CSO.
About the IASLC:
The International Association for the Study of Lung Cancer (IASLC) is the only global organization dedicated solely to the study of lung cancer and other thoracic malignancies. Founded in 1974, the association's membership includes more than 8,000 lung cancer specialists across all disciplines in over 100 countries, forming a global network working together to conquer lung and thoracic cancers worldwide. The association also publishes the Journal of Thoracic Oncology, the primary educational and informational publication for topics relevant to the prevention, detection, diagnosis, and treatment of all thoracic malignancies. Visit www.iaslc.org for more information.
About the WCLC:
The WCLC is the world’s largest meeting dedicated to lung cancer and other thoracic malignancies, attracting more than 7,000 researchers, physicians and specialists from more than 100 countries. The goal is to increase awareness, collaboration and understanding of lung cancer, and to help participants implement the latest developments across the globe. The conference will cover a wide range of disciplines and unveil several research studies and clinical trial results. For more information, visit wclc2020.iaslc.org.