Survival outcomes of PD1/PDL1 inhibitor-based regimens in unresectable stage IIIB, IIIC, and IV non-small cell lung cancer.
Abstract
e20569 Background: The five-year survival for patients with unresectable Stage IIIB and IIIC non–small cell lung cancer (NSCLC) ranges from 12% to 26%, decreasing to 16% in Stage IV. The introduction of PD-1/PD-L1 inhibitors has changed the therapeutic approach for advanced NSCLC. We aimed to evaluate the survival outcomes of PD-1/PD-L1 inhibitor-based regimens in unresectable Stage IIIB, IIIC, and IV NSCLC. Methods: We conducted a retrospective analysis of adults with unresectable NSCLC treated with PD1/PDL1 inhibitors at a community-based Southern U.S. Health System from 2018 to 2024. Patients were categorized into PD1/PDL1 inhibitor Monotherapy (Group A), Dual-Modality with a PD1/PDL1 inhibitor plus chemotherapy (Group B), and Intensified Multi-agent Therapy (Group C), which included patients who received more than one agent: PD1/PDL1 inhibitors, anti-VEGF, or CTLA4 inhibitor with or without chemotherapy (Group C). A log-logistic survival model adjusted for sociodemographic and comorbidities was used to estimate the adjusted event time ratio (aETR). Results: A total of 133 patients met the inclusion criteria and were categorized into three treatment groups: A (21%), B (64.7%), and C (14.3%). The median age across the three groups was 72 years, 67 years, and 64 years, respectively. The most common PD1/PDL1 inhibitor was pembrolizumab in Groups A (67.9%) and B (67.4%). In Group C, 68.4% received more than one PD1/PDL1 inhibitor, and durvalumab was the most common agent (47.4%). PDL1 expression of more than 50% was seen in 69.2%, 29%, and 11.8% of Groups A, B, and C, respectively. The median survival was 16.2, 10.3, and 24.7 months. Mortality peaked earliest in Group B and latest in Group C during the duration of therapy. The survival model showed no significant difference in the expected survival between Groups A and B (aETR=1.66, 95% CI 0.92–2.99, P>0.05), Groups B and C (aETR=0.53, 95% CI 0.28–0.99, P=0.1), and Groups A and C (aETR=0.88, 95% CI 0.4–1.91, P>0.05). In patients with metastatic disease, the median survival was 16.2, 11.0, and 29.1 months. Mortality peaked earliest in Group B and latest in Group C. The survival model showed no significant difference in the expected survival between Groups A and B (aETR=1.54, 95% CI 0.89-2.66, P>0.05) and Groups A and C (aETR=0.71, 95% CI 0.34-1.51, P>0.05). Group B had a 53.6% lower expected survival (aETR=0.46, 95% CI 0.25-0.87, P=0.047) compared to Group C. Conclusions: Patients with unresectable Stage IIIB, IIIC, and IV non–small cell lung cancer treated with PD1/PDL1 inhibitor monotherapy and multi-agent therapy had longer survival compared to those receiving dual treatment. In patients with metastatic disease, multi-agent therapy had the longest survival of all three regimens. These findings support the benefit of PD1/PDL1 inhibitors. Prospective studies are needed to study its use as direct therapy and as neoadjuvant treatment.
Article Details
Journal Info
Journal of Clinical Oncology
Lippincott Williams & Wilkins
Authors (7)
Barath Prashanth Sivasubramanian
Northeast Georgia Medical Center, Gainesville, GA
Chiugo Okoye
2Northeast Georgia Medical Center. Gainesville. GA 30501, Gainesville. GA 30501, United States
Palwasha Khan
Shikha Upreti
Northeast Georgia Medical Center, Gainesville, GA
Hardeep Singh
Jake Slaton
Northeast Georgia Medical Center, Gainesville, Georgia, United States
Charles H. Nash
Northeast Georgia Medical Center, Gainesville, GA