1 research outputs found
Realâworld treatment patterns and clinical outcomes after introduction of immune checkpoint inhibitors: Results from a retrospective chart review of patients with advanced/metastatic nonâsmall cell lung cancer in the EU5
Abstract Background Realâworld evidence is increasingly used to guide treatment and regulatory decisions for nonâsmall cell lung cancer (NSCLC). Realâworld treatment patterns and clinical outcomes among patients with advanced/metastatic NSCLC in France, Germany, Italy, Spain, and the UK (EU5) were assessed. Methods This retrospective physicianâcompleted patient chart review assessed treatment patterns (regimen, duration of treatment [DOT], time to discontinuation), and clinical outcomes (duration of response [DOR], progressionâfree survival [PFS], and overall survival [OS]) of patients with stage IIIB/C or IV NSCLC who received pembrolizumabâbased firstâline induction chemotherapy. Results Overall, 322 patients were included; at firstâline maintenance (1LM), 92% had stage IV NSCLC, 68% had nonsquamous histology, and 89% had no central nervous system (CNS)/brain metastasis. The two most common 1LM regimens were pembrolizumab monotherapy (76% overall) and pembrolizumab + pemetrexed (21% overall). Docetaxel monotherapy was the most common secondâline regimen in all countries except Germany (54% overall). For 1LM therapy, the overall median DOT and DOR were 5 and 10âmonths, respectively; PFS was 7âmonths and OS was 8âmonths. Germany had a longer duration of each outcome except for DOR which was longer in Spain. Clinical outcomes were generally poorer for patients with squamous histology and CNS/brain metastases. Conclusions This study demonstrated differences in treatment patterns and clinical outcomes in NSCLC across the EU5 and patient subgroups. Improved survival was generally associated with response to firstâline therapy, nonsquamous histology, and CNS/brain metastases absence. These realâworld data provide valuable insights which may aid treatment decisionâmaking and clinical trial design