• Curr Med Res Opin · Jul 2024

    Multicenter Study

    Evaluation of the efficacy and safety of nivolumab in the second- or later-line treatment of patients with locally advanced/metastatic non-small cell lung cancer in Türkiye: a retrospective multicenter non-interventional registry study.

    • Nuri Karadurmus, Muhammet Ali Kaplan, SendurMehmet Ali NahitMANDepartment of Medical Oncology, Ankara City Hospital, Ankara, Türkiye., Yuksel Urun, Umut Demirci, Saziye Burcak Karaca, Sabin Goktas Aydin, Musa Baris Aykan, Ahmet Bilici, Ahmet Sezer, Ulku Yilmaz, Huseyin Abali, Perran Fulden Yumuk, Serkan Degirmencioglu, Ahmet Demirkazik, Semra Paydas, Cem Mirili, Hande Turna, Aysegul Kargi, Mustafa Ozdogan, Deniz Can Guven, Mustafa Ozguroglu, and Saadettin Kilickap.
    • Medical Oncology Department, University of Health Sciences, Gulhane Training and Research Hospital, Ankara, Türkiye.
    • Curr Med Res Opin. 2024 Jul 1; 40 (7): 117111781171-1178.

    ObjectiveTo evaluate the efficacy and safety of nivolumab in the second-line (2L) or later-line (LL) treatment of patients with locally advanced/metastatic non-small cell lung cancer (NSCLC) in real-life setting in Türkiye.MethodsThis study was designed as a national, multi-center, retrospective study. The study population was evaluated in two groups for the line of nivolumab therapy: those receiving nivolumab in the 2L (Group 2L) and third-line (3L) or LL (Group 3L/LL). Efficacy was evaluated based on one-year overall survival (OS) and progression-free survival (PFS). Safety was evaluated based on treatment-related adverse events (AEs) and nivolumab discontinuation rate.ResultsOf 244 patients, 52.9% were in Group 2L and 47.1% were in Group 3L/LL. Demographic and clinical characteristics did not differ between the groups. In Group 2L and Group 3L/LL, one-year OS and PFS rates were 60.8% and 61.4% (p = 0.592) and 31.2% and 21.3% (p = 0.078), respectively. The objective response rate (ORR) was 34.7% in Group 2L and 27.3% in Group 3L/LL (p = 0.262). The percentage of patients reporting at least one AE in Groups 2L and 3L/LL was 34.9% and 43.5%, respectively (p = 0.169). Fatigue was the most common (16.4%) treatment-related AE in each group. The groups were comparable regarding the AE frequency. Nivolumab was discontinued in 61 patients in Group 2L and 53 patients in Group 3L/LL, with the most common reason being disease progression (57.4% and 66.0%, respectively).ConclusionNivolumab is safe and effective in the 2L or 3L/LL treatment of locally advanced/metastatic NSCLC and associated with acceptable AEs in real-life setting.

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