Journal of Global Oncology (May 2019)

Overall Survival of Patients With ALK-Positive Metastatic Non–Small-Cell Lung Cancer in the Russian Federation: Nationwide Cohort Study

  • Ilya Tsimafeyeu,
  • Fedor Moiseenko,
  • Sergei Orlov,
  • Elena Filippova,
  • Alexander Belonogov,
  • Aleksey Nebesnykh,
  • Amir Khalimov,
  • Elena Karabina,
  • Valentina Shikina,
  • Ahmed Abdelgafur,
  • Galina Statsenko,
  • Irina Titova,
  • Dmitry Isaichikov,
  • Galina Makarnyaeva,
  • Aleksey Mordovskiy,
  • Oksana Barkovskaya,
  • Aleksey Smirnov,
  • Marina Gikalo,
  • Nikita Savelov,
  • Dmitry Kosov,
  • Evgeny Imyanitov,
  • Irina Demidova,
  • Sergei Tjulandin

DOI
https://doi.org/10.1200/JGO.19.00024
Journal volume & issue
Vol. 5
pp. 1 – 7

Abstract

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PURPOSE: The overall survival (OS) results in patients with ALK-positive metastatic non–small-cell lung cancer (NSCLC) have rarely been reported. The aim of this prospective-retrospective cohort study was to obtain real-world data on the use of crizotinib or chemotherapy in patients with ALK-positive metastatic NSCLC in Russia. PATIENTS AND METHODS: Patients with epidermal growth factor receptor–negative metastatic NSCLC were screened in 23 cancer centers. To be eligible, patients were required to have confirmation of ALK rearrangement. Patients were treated with crizotinib (250 mg twice daily; n = 96) or the investigator’s choice of platinum-based chemotherapy (n = 53). The primary end point was OS. RESULTS: A total of 149 ALK-positive patients were included. Mean age was 53 years in both groups. Patients were predominately women (59%) and never-smokers (74%), and most patients had adenocarcinoma histology (95%). At a median follow-up time of 15 months, 79 of the 149 patients included in the analysis had died. Median OS from the start of treatment was 31 months (95% CI, 28.5 to 33.5 months) in the crizotinib group and 15.0 months (95% CI, 9.0 to 21.0 months) in the chemotherapy group (P < .001). The objective response rate was 34% in the crizotinib group. Among patients with brain metastasis, one complete response (6%) and five partial responses (31%) were achieved. Grade 3 adverse events were observed in three patients (3%) in the crizotinib group. CONCLUSION: The improved OS observed in crizotinib clinical trials in ALK-positive NSCLC was also observed in the less selective patient populations treated in daily practice in Russia. The use of standard chemotherapy in these patients remains common but seems inappropriate as a result of the effectiveness of newer treatments, such as crizotinib.