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NCT03979170Recruiting

Patient-derived Organoids of Lung Cancer to Test Drug Response

Summary

This is a single center, single arm, open and exploratory clinical study, with 50 cases planned for a period of 3 years. The purpose of this study is to evaluate the consistency and accuracy of a Patient-Derived Organoid (PDO) Model of lung cancer to predict the clinical efficacy of anti-cancer drugs, in order to predict the best chemotherapy regimen for each given patient.

Inclusion criteria

• Histologically proven lung cancer • Age ≥ 18 • Written informed and signed consent • Accessible to biopsy and/or surgery sample of metastasis and/or primitive tumour

Exclusion criteria

• Less than 18 years of age • Not able to give informed consent (language, intellectual capacities, etc.) • Not accessible to biopsy and/or surgery sample • Not enough lung tissue for a histological analysis or the remaining lung tissue is not enough to perform a routine pathological analysis.

Contacts

The trial team's contact details are shown on request.

See the official trial record
Status
Recruiting
Phase
—
Study type
Observational
Countries
Switzerland
Sponsor
University Hospital, Geneva(Other)
Protocol no.
2018-02395
Conditions
Lung Cancer, Organoid
Interventions
Procedure

Treatments studied

  • Lung tumor resection

Locations · 1

  • Geneva, SwitzerlandGeneva University HospitalsRecruiting at this site

In total, worldwide, the only site listed in the registry is recruiting.

Site status per the ClinicalTrials.gov registry (last update posted: June 3, 2024).

This status may have changed and says nothing about your eligibility: before taking any step, check with your oncologist or the site.

Other identifiers

  • 2018 · NIH grant

See also

Other versions

These results are indicative and do not replace medical advice — discuss them with your doctor.