Does Nivolumab for progressed metastatic lung cancer fulfills its promises? An efficacy and safety analysis in 20 general hospitals
Menée aux Pays-Bas à partir de données portant sur 267 patients traités dans 20 hôpitaux et atteints d'un cancer du poumon non à petites cellules réfractaire ou récidivant après une chimiothérapie de première ligne, cette étude évalue l'efficacité, dans un contexte de vie réelle et du point de vue de l'amélioration de la survie globale et de la survie sans progression, et la toxicité du nivolumab, en comparant ces résultats à ceux des essais de phase III
Objectives : In patients with refractory or recurrent non-small-cell lung cancer (NSCLC) after first line chemotherapy, phase III trials showed superiority of nivolumab, an IgG4 programmed death-1 immune-checkpoint-inhibitor antibody, over docetaxel. We evaluated case mix, effectiveness and safety of nivolumab upon implementation in general practice. Materials and Methods : In 20 general hospitals, all consecutive NSCLC patients treated with nivolumab within the medical need program (inclusion period 12 months) in Flanders − Belgium were evaluated. Results : There were 267 patients, Eastern Cooperative Oncology Group (ECOG) score was 2 in 24% and 0-1 in 76%. In 48%, two or more systemic regimens were given before nivolumab. The median overall survival was 7.8 months (95% confidence interval (CI) 6.3-9.3). At one year, the overall survival rate was 36.5 ± 0.34%. Median progression-free survival was 3.7 months (95% CI 2.9-4.5). An objective response was obtained in 23.2%. ECOG score 2 and presence of liver metastasis strongly correlated with worse survival (p<0.00001). Treatment related adverse events grade 3 or 4 were reported in 21%, colitis (4%) and pneumonitis (7%) were most frequent. Conclusion : Upon implementation of nivolumab therapy in general hospitals, the case mix was characterized by a more heavily pretreated population with a substantial fraction of patients with ECOG score 2. The median overall survival is slightly inferior to what was published in the randomized phase III trials. An ECOG score 2 and the presence of liver metastasis correlated strongly with a worse survival. We report a high prevalence of serious adverse events.
Lung Cancer 2017