Patient Derived Preclinical Models

Обзор

Study goal is to collect tumor specimens that may inform cancer biology to eventually improve outcomes for patients with cancer. This proposal represents a highly collaborative effort to support cancer research with the goal of developing novel therapeutic strategies using patient derived preclinical models. This study is being done to collect samples of tumor tissues, matched normal tissue when possible, and approximately 50 mL of blood.

Подробное описание

The objective of this study is to collect tumor specimens (tumor tissues, matched normal tissue when possible, and 50 mL of blood) that may inform cancer biology to eventually improve outcomes for patients with cancer. Additionally, relevant specimens that were previously collected under an IRB approved protocol (13-000942), will be used with approval of the PI of that protocol and patient consent for participation in this protocol.

The collected tissue specimens will be used to develop preclinical models; i.e., cell lines, patient derived micro-cancer models as well as patient-derived xenograft models. In this study we may profile tumors using genomic and/or proteomic approaches to identify targetable alterations in tumor tissue from patients. To assure that the derived cell lines and micro-cancer models have not been cross contaminated during development with other models in development, DNA sequencing may be used. Using these preclinical models, we will test new therapies in vitro, or in vivo in mice in order to identify novel therapeutics as well as interrogate genes for their role in tumor biology. Guidance for molecular targeted therapy will involve gene analysis of oncogenes and tumor suppressor genes. Results from these studies may provide the rationale for the design of future novel clinical trials. The evaluation of these preclinical models may lead to predictive value related to patient response to therapy as well as clinical trials. With consent, these models may be shared with other investigators internal or external to Mayo Clinic.

Вмешательства

• Процедура Tissue Collection
  Research tissue specimen will be obtained during the patient's clinical biopsy or clinical tumor resection, if feasible.
• Диагностический тест Blood Collection
  Up to 50 mL of research blood will be drawn around the time of the procedure. Additional blood may be collected in selected cases, as warranted, to monitor disease recurrence/remission or perform additional
• Диагностический тест Buccal Swab
  Buccal swab may be requested, if necessary, to generate germline data.

Первичные конечные точки

• Number of participants accrued with genomic, microbiome, and drug sensitivity components of aggressive cancer. [Срок оценки: Up to 6 years post tissue and blood collection]

Вторичные конечные точки (1)

• Determine number of participants with genomic, microbiome and drug sensitivity assays (profile or functional) that suggest changes to treatment plan. [Срок оценки: Up to 6 years post tissue and blood collection]

Критерии участия

Критерии включения

• 18 years of age and older
• Patient is a good medical candidate for a standard of care or research biopsy or surgical procedure to obtain tissue

Критерии исключения

• Uncontrolled concurrent illness including psychiatric illness, or situations that would limit compliance with the study requirements or the ability to willingly give written informed consent
• Institutionalized or incarcerated patients
• Inaccessible tumor for biopsy or patient does not have tumor tissue available for research use
• Biopsy must not be considered more than minimal risk to the patient.
• Have a contraindication to percutaneous biopsy including:

• Significant coagulopathy that cannot be adequately corrected.
• Severely compromised cardiopulmonary function or hemodynamic instability.
• Lack of a safe pathway to the lesion per the interventional radiologist.
• Inability of the patient to cooperate with, or to be positioned for, the procedure.

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Нет

Дизайн исследования

Модель наблюдения

Другое

Центры проведения

США · 1 центр

• Mayo Clinic in Rochester — Rochester

Идентификаторы

NCT: NCT05324553 · 21-008831

Первоисточники (государственные реестры)

• ClinicalTrials.gov (NIH, США)

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