Planned study population consists of approximately 1500 adult patients with a/m NSCLC inRussia, in about 20 oncological centers (in each center it is expected to recruit about75 patients) in different regions of Russia in order to provide representative studysample
Not Provided
Inclusion Criteria:
1. Morphologically confirmed NSCLC with or without actionable genomic alterations (AGA,
i.e. EGFR, ALK, ROS1, NTRK, BRAF, MET exon 14 skipping, RET, ERBB2 (HER2), or KRAS)
2. Age ≥18 years at the time of NSCLC diagnosis;
3. Locally advanced or metastatic disease defined as incident stage IIIB/IIIC/IV NSCLC
or stage I-IIIA then progressed to stage IIIB-IV disease and not eligible for
curative-intent treatment (the date of progression is included in the database);
4. Available data on at least one line of systemic therapy for advanced/metastatic
disease within the period since January 2022 until January 2025;
5. Patients may be alive or deceased at the time of medical record abstraction
Exclusion Criteria:
1. Patients participated or participating in clinical trials or any early access
program within period since the index date until the end of study period;
2. Diagnosis of another cancer (except for melanoma/skin cancer) at or within 5 years
prior to NSCLC diagnosis or any ongoing systemic anti-cancer therapy regimen at the
time of NSCLC diagnosis
Research Site
Arkhangelsk, Russia
Research Site
Barnaul, Russia
Research Site
Irkutsk, Russia
Research Site
Kemerovo, Russia
Research Site
Kostroma, Russia
Research Site
Krasnoyarsk, Russia
Research Site
Moscow, Russia
Research Site
Novokuznetsk, Russia
Research Site
Novosibirsk, Russia
Research Site
Obninsk, Russia
Research Site
Perm, Russia
Research Site
Saint Petersburg, Russia
Research Site
Ufa, Russia
Research Site
Vladivostok, Russia
Research Site
Yaroslavl, Russia
Research Site
Yekaterinburg, Russia
Not Provided