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LUng CAncer focuS - Long-term Monitoring of Bronchogenic Carcinoma Patients (LUCAS)

LUng CAncer focuS - Long Term Non-interventional Monitoring of Diagnostic and Treatment Patterns in Patients With Bronchogenic Carcinoma (LUCAS)

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04228237
Acronym
LUCAS
Enrollment
2300
Registered
2020-01-14
Start date
2018-06-01
Completion date
2025-05-31
Last updated
2022-03-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Lung Cancer

Keywords

lung cancer, bronchogenic carcinoma, diagnosis, treatment, non-interventional

Brief summary

Long-term non-interventional monitoring of diagnostics and treatment patterns in newly diagnosed patients in selected pneumology centers in Czech republic.

Detailed description

Diagnosis, treatment and care of patients with bronchogenic carcinoma (BCA) is, as with most other oncological diseases, a complex multidisciplinary process. Due to the lack of information on the speed and success of the initial diagnosis, the use of the necessary laboratory techniques, and the individual therapeutic steps leading to cure or medical failure, the Czech Pneumological and Phtizeology Society (CPPS) decided to carry out long-term non-interventional monitoring of newly diagnosed patients. This monitoring is non-interventional, so the usual diagnostic and therapeutic procedures will be used according to the decision of the physician. All patients with bronchogenic carcinoma diagnosed from June 1, 2018 will be enrolled with up to 60 months of follow-up.

Interventions

None listed

Sponsors

OAKS Consulting s.r.o.
CollaboratorUNKNOWN
Ceska Lekarska Spolecnost Jana Evangelisty Purkyne z.s.
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

\- clinical diagnosis of lung cancer (C34 in MKN classification)

Design outcomes

Primary

MeasureTime frameDescription
Overall survival (OS)60 months of follow-upTime from randomization until death from any cause
Progression-free survival (PFS)any treatment during 60 months of follow-upTime from randomization until disease progression or death
Time to treatment discontinuation (TTD)any treatment during 60 months of follow-uptime from starting a medication until treatment discontinuation or death

Secondary

MeasureTime frameDescription
Time to next treatment (TTNT)60 months of follow-upTime from end of primary treatment to institution of next therapy

Countries

Czechia

Contacts

Primary ContactJana Alahakoon
jana.alahakoon@oaks.cz+420602350988
Backup ContactJaroslav Duba
jaroslav.duba@oaks.cz+420606613224

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 20, 2026