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LALUCA Research Platform A Prospective Analysis of Lung Cancer Diagnosis and Management in Clinical Practice

Landsteiner Lung Cancer Research Platform (LALUCA) A Prospective Analysis of Lung Cancer Diagnosis and Management in Clinical Practice

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04733430
Acronym
LALUCA
Enrollment
500
Registered
2021-02-02
Start date
2020-04-17
Completion date
2030-04-30
Last updated
2024-03-18

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

Conditions

Lung Cancer

Keywords

NGS Testing

Brief summary

This is a prospective analysis of the diagnosis and treatment of lung cancer in a real-world setting. The aim of the project is to establish a clinical platform to collect representative data on molecular testing, sequence of systemic tumor therapy and other therapies, and disease progression of patients with lung cancer. A special focus will be on molecular biomarker testing and reflex NGS testing. Another aim of the registry is the collection of quality indicators in lung cancer care. The results of the register will be used to describe the current state of care and to develop it further for the future.

Detailed description

The identification of driver-mutations, whose gene product can be specifically inhibited by targeted therapies, has markedly changed the diagnostic and therapeutic landscape for this tumor entity, leading to improved outcomes for patients with metastatic NSCLC. The use of next generation sequencing (NGS) allows for detection of a multitude of different druggable mutations. In absence of a curative treatment approach and a druggable mutation the prognosis of lung cancer remains poor. Thorough knowledge of the treatment reality, e.g. characteristics, diagnostic, treatment and outcome of unselected patients in real-Iife practice, is crucial to evaluate and improve the quality of care for patients with lung cancer. The purpose of this project is to set up a clinical platform to document representative data on molecular testing, sequence of systemic treatment and other treatment modalities, and course of disease in patients with lung cancer. A particular focus is on molecular biomarker testing and NGS of patients before the start of first-line treatment. The data shall be used to assess the current state of care and to develop recommendations concerning topics that can be improved.

Interventions

None listed

Sponsors

Karl Landsteiner Institute for Lung Research and Pneumological Oncology
Lead SponsorOTHER

Study design

Observational model
ECOLOGIC_OR_COMMUNITY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 125 Years
Healthy volunteers
No

Inclusion criteria

* Informed consent * Histologically confirmed lung cancer * Age ≥ 18 years * Able to understand and willing to sign written Informed Consent and to complete patient-reported-outcome assessment instruments

Exclusion criteria

\-

Design outcomes

Primary

MeasureTime frameDescription
NGS Testingthrough study completion, an average of 5 yearsTo assess molecular biomarker testing and indicators of the quality of care in patients with lung cancer

Countries

Austria

Contacts

Primary ContactGeorg-Christian Funk, MD
georg-christian.funk@gesundheitsverbund.at+43 1 4000-2203
Backup ContactAgnes Attoh, BSc
agnes.attoh@extern.gesundheitsverbund.at+43 1 4000-72203

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026