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 581049, Russia
Research Site
Barnaul 1510853, Russia
Research Site
Irkutsk 2023469, Russia
Research Site
Kemerovo 1503901, Russia
Research Site
Kostroma 543878, Russia
Research Site
Krasnoyarsk 1502026, Russia
Research Site
Moscow 524901, Russia
Research Site
Novokuznetsk 1496990, Russia
Research Site
Novosibirsk 1496747, Russia
Research Site
Obninsk 516436, Russia
Research Site
Perm 511196, Russia
Research Site
Saint Petersburg 498817, Russia
Research Site
Ufa 479561, Russia
Research Site
Vladivostok 2013348, Russia
Research Site
Yaroslavl 468902, Russia
Research Site
Yekaterinburg 1486209, Russia
Not Provided