Russian lung cancer study reveals Real-World treatment patterns
NCT ID NCT05887011
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study observes how doctors in Russia treat inoperable lung cancer (NSCLC and SCLC) using chemoradiotherapy. Researchers will collect data from 2000 patients across 50 cancer centers to understand real-world practices and short-term outcomes. No new treatments are given; the goal is to learn from existing medical records.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 2,000 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Mar 2023
- Expected to finish
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Jun 2026
An estimate. End dates often move.
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
The study will include 2000 patients who received chemoradiotherapy (cCRT or sCRT) for the treatment of locally advanced NSCLC and SCLC in 50 largest oncology centers in Russian Federation. The total enrolment period will take up to 2 years. Information about specific NSCLC or SCLC treatments following CRT (e.g., durvalumab) will not be collected in the study.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Age ≥ 18 years old 2. Provision of written informed consent 3. Patient received at least one RT dose under prescribed CRT (concurrent or sequential) for definitive treatment of locally advanced NSCLC (stage II-III, unresectable or inoperable NSCLC, including locoregional recurrence and patient's refusal to undergo surgery) or LS-SCLC based on local MDT decision 4. Patient is currently undergoing RT (preferably no more than 10 doses) Exclusion Criteria: 1. Participation in another clinical study with an investigational product during the last 3 months 2. Confirmation that the subject was already included in this study before 3. Absence of written informed consent form 4. Data erroneously collected from subjects for which written consent is not available, will not be included in or will be deleted from the study database.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Research Site
Arkhangelsk, Russia
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Research Site
Balashikha, Russia
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Research Site
Barnaul, Russia
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Research Site
Grozny, Russia
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Research Site
Irkutsk, Russia
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Research Site
Ivanovo, Russia
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Research Site
Kaluga, Russia
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Research Site
Kazan', Russia
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Research Site
Kemerovo, Russia
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Research Site
Khabarovsk, Russia
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Research Site
Khanty-Mansiysk, Russia
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Research Site
Kirov, Russia
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Research Site
Kostroma, Russia
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Research Site
Krasnodar, Russia
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Research Site
Krasnoyarsk, Russia
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Research Site
Moscow, Russia
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Research Site
Nizhny Novgorod, Russia
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Research Site
Novokuznetsk, Russia
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Research Site
Novosibirsk, Russia
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Research Site
Obninsk, Russia
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Research Site
Perm, Russia
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Research Site
Podolsk, Russia
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Research Site
Rostov-on-Don, Russia
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Research Site
Ryazan, Russia
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Research Site
Saint Petersburg, Russia
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Research Site
Saransk, Russia
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Research Site
Saratov, Russia
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Research Site
Sochi, Russia
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Research Site
Tula, Russia
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Research Site
Tver', Russia
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Research Site
Ulyanovsk, Russia
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Research Site
Vladivostok, Russia
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Research Site
Vologda, Russia
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Research Site
Yakutia, Russia
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Research Site
Yaroslavl, Russia
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Research Site
Yekaterinburg, Russia
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Research Site
Yuzhno-Sakhalinsk, Russia
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