Patient-derived Organoid Model and Circulating Tumor Cells for Treatment Response of Lung Cancer

ConditionLung Neoplasm
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorThe University of Texas Health Science Center at San Antonio

About this trial

Create a living biobank of PDOs from Stage I-III lung cancer patients.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Read, consented to and signed the IRB-approved informed consent form prior to any study related procedure.

Diagnosis of lung cancer or lung mass or lymphadenopathy that will either systemic treatment or tumor resection as part of standard of care

Any clinical stage of lung cancer

Adult patients ≥18 years of age

Disqualifiers

At the discretion of the treating physician, patient will not be able to fulfill the requirements of the study.

Trial population

Lung cancer patients

Trial design

Design model

Other

Time perspective

Prospective

Treatments tested in this trial

  • Lung Tumor Resection

    Procedure/Surgery

    Lung Tumor Resection

Treatment groups

No treatment groups listed

Trial outcomes

Primary outcomes

1

To establish and characterize a biobank of patient-derived organoids (PDOs), and investigate the potential of PDOs to recapitulate ex vivo responses to chemotherapeutic and targeted agents observed in the clinic.

Establishment of a living biobank of PDOs and the potential of PDOs to repeat their process outside a living organism

Time frame
10 years

Secondary outcomes

1

Correlation of PDO and Circulating tumor cells (CTCs)

To establish a connection between PDOs and CTCs, and their relationship to cancer

Time frame
10 years

Other outcomes

Sponsors and contacts

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