Effectiveness of crizotinib in patients with ROS1 -positive non-small-cell lung cancer: real-world evidence in Japan.
Naoyuki NogamiAtsushi NakamuraNaoko ShiraiwaHironori KikkawaBirol EmirRobin WiltshireMasahiro MorisePublished in: Future oncology (London, England) (2023)
Aim: Crizotinib, approved in Japan (2017) for ROS1 -positive NSCLC, has limited real-world data. Materials & methods: Crizotinib monotherapy real-world effectiveness and treatment status were analyzed from claims data (June 2017-March 2021; Japanese Medical Data Vision; 58 patients tested for ROS1 -NSCLC). Results: Median duration of treatment ([DoT]; primary end point), any line: 12.9 months; 22 patients on crizotinib, 23 discontinued, 13 receiving post-crizotinib treatment. 1L (n = 27) median DoT: 13.0 months (95% CI, 4.4-32.0 months); 13 patients on crizotinib; seven discontinued; seven receiving post-crizotinib treatment. 2L (n = 13) median DoT: 14.0 months (95% CI, 4.6-22.2 months); 2L+ (n = 31): nine patients on crizotinib; 16 discontinued; six receiving post-crizotinib treatment. Post-crizotinib treatments (chemotherapy, cancer immunotherapy, anti-VEGF/R) did not affect crizotinib DoT. Conclusion: Data supplement crizotinib's effectiveness in ROS1 -positive NSCLC previously seen in clinical trials/real-world.
Keyphrases
- advanced non small cell lung cancer
- end stage renal disease
- ejection fraction
- newly diagnosed
- small cell lung cancer
- chronic kidney disease
- clinical trial
- systematic review
- prognostic factors
- dna damage
- healthcare
- electronic health record
- squamous cell carcinoma
- big data
- oxidative stress
- reactive oxygen species
- radiation therapy
- study protocol
- health insurance
- vascular endothelial growth factor
- rectal cancer
- open label
- data analysis
- brain metastases