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Набор скоро начнётся NCT06895681

UCSF Biobank for Hereditary Cancers and Tumor-Associated Mutations

— Наблюдательное Solid Tumor Solid Tumor, Adult Somatic Mutation Solid Tumor, Unspecified, Adult

Ориентир для пациента и семьи

Простыми словами

Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.

Что изучают
В протоколе указаны: Blood Sample, Tissue Sample, Excess fluid Sample, Medical Chart Review.
Кому может быть актуально
Состояния в реестре: Solid Tumor, Solid Tumor, Adult, Somatic Mutation, Solid Tumor, Unspecified, Adult. Базовые параметры: от 18 лет · Все.
Что важно проверить
Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
Где проводится
США
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →

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Официальное название

UCSF Biobank for Studying Hereditary Cancers and Tumor-Associated Mutations

Обзор

This is a non-therapeutic clinical research biorepository protocol designed to obtain, store, and clinically annotate biospecimens from participants with hereditary cancers. Those biospecimens will be used to generate participant-derived tumor models that will serve as a resource to better understand hereditary cancers and develop new efficient therapies.

Подробное описание

Primary Objective:

1. To generate a repository of participant-derived tumor models\* and specimens\*\* - annotated with demographic, clinical, and pathologic data - from adults with solid tumor malignancies with germline or somatic tumor-associated mutations and/or a personal or family history of cancer.

* Participant-derived models may include (but are not limited to) xenografts (PDX), organoids (PDO), and cell lines (PDCLs).

* Specimens may include tissue, ascites and pleural fluid, and blood.

Exploratory Objectives

1. To correlate in vivo drug sensitivity of participant-derived models with patient clinical response. 2. To conduct blood-based assessment of tumor-associated biomarkers (DNA/RNA/protein, etc.). 3. To describe tumor and blood-based biomarkers that are predictive of clinical response. 4. To correlate changes in tumor and blood-based biomarker expression with clinical outcomes over time. 5. To perform genomic and transcriptomic profiling of banked specimens and correlate findings with clinical outcomes, prognostic markers, and biomarkers. 6. Unspecified cancer-centric research in the Munster Lab and other future unspecified research.

OUTLINE:

Participants will have biospecimens collected at non-study, routine procedures or visits to be stored at UCSF. Specimens will be processed and banked as per standard operating procedure. Participants will be followed through medical record chart review for a period of 10 years after signing informed consent, and be contacted every 3 months (± 2 months) for the first year and every 6 months (± 3 months) thereafter to allow updates to health status.

Вмешательства

  • Процедура Blood Sample
    Obtained at the time of non-study related routine blood draw.
  • Процедура Tissue Sample
    Obtained at the time of non-study related routine biopsy or surgical procedure.
  • Процедура Excess fluid Sample
    Obtained at the time of non-study related routine biopsy, surgical procedure, paracentesis, or thoracentesis procedure.
  • Другое Medical Chart Review
    Demographic, clinical, and pathologic information will be extracted from the medical record

Первичные конечные точки

  • Develop participant-derived tumor models of hereditary cancers [Срок оценки: Up to 10 years]

Критерии участия

Критерии включения

For participants undergoing collection of tissue, ascites, and/or pleural effusions:

  • Ability to understand and willingness to voluntarily sign a written informed consent document prior to any study-related assessments or procedures are conducted.
  • Individuals 18 years of age or older on the day of signing informed consent.
  • Individuals with solid tumor malignancy with germline or somatic cancer-associated mutations and/or Individuals with a family history or personal history of cancer.
  • Must be planning to undergo one of the following procedures as part of their routine care (or as a research procedure under a UCSF-sponsored IIT protocol):
  • Surgical resection
  • Biopsy (open, incisional, excisional, punch, core needle, and/or fine needle aspiration (FNA) are all permitted)
  • Paracentesis
  • Thoracentesis

For participants undergoing blood banking:

  • Ability to understand and willingness to voluntarily sign a written informed consent document prior to any study-related assessments or procedures are conducted.
  • Individuals 18 years of age or older on the day of signing informed consent.
  • Individuals with a family history or personal history of cancer.
  • Must be planning to undergo a blood draw as part of their routine care (or as a research procedure under a University of California, San Francisco (UCSF) -sponsored investigator-initiated trial (IIT) protocol); or willing to undergo an additional blood draw outside of their routine care.

Критерии исключения

1\. Known history of HIV, Hepatitis B, or Hepatitis C (as documented in the medical record) or other infectious disease that in the judgment of the investigator could pose a risk to research personnel or mice, or negatively impact Patient derived xenografts (PDX) tumor engraftment.

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

Здоровые добровольцы: Нет

Дизайн исследования

Модель наблюдения
Случай-контроль

Центры проведения

США · 1 центр
  • University of California, San Francisco — San Francisco

Идентификаторы

NCT: NCT06895681 · 24986

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗