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Trial record 1 of 1 for:    A212102 Blinded Reference Set For Multicancer Early Detection Blood Tests
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Collecting Blood Samples From Patients With and Without Cancer to Evaluate Tests for Early Cancer Detection

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ClinicalTrials.gov Identifier: NCT05334069
Recruitment Status : Recruiting
First Posted : April 19, 2022
Last Update Posted : March 17, 2023
Sponsor:
Collaborator:
National Cancer Institute (NCI)
Information provided by (Responsible Party):
Alliance for Clinical Trials in Oncology

Study Description
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Top of Page Study Description Study Design Groups and Cohorts Outcome Measures Eligibility Criteria Contacts and Locations More Information
Brief Summary:
This study collects blood and tissue samples from patients with cancer and without cancer to evaluate tests for early cancer detection. Collecting and storing samples of blood and tissue from patients with and without cancer to study in the laboratory may help researchers develop tests for the early detection of cancers.

Condition or disease Intervention/treatment
Acute Lymphoblastic Leukemia Acute Myeloid Leukemia Ann Arbor Stage I Lymphoma Ann Arbor Stage II Lymphoma Ann Arbor Stage III Lymphoma Ann Arbor Stage IV Lymphoma Chronic Lymphocytic Leukemia Chronic Myeloid Leukemia Gastroesophageal Junction Adenocarcinoma Head and Neck Carcinoma Hematopoietic and Lymphoid Cell Neoplasm Invasive Breast Carcinoma Kidney Carcinoma Malignant Hepatobiliary Neoplasm Malignant Solid Neoplasm Melanoma Muscle-Invasive Bladder Carcinoma RISS Stage I Plasma Cell Myeloma RISS Stage II Plasma Cell Myeloma RISS Stage III Plasma Cell Myeloma Sarcoma Stage I Bladder Cancer AJCC v6 and v7 Stage I Breast Cancer AJCC v7 Stage I Colorectal Cancer AJCC v6 and v7 Stage I Esophageal Cancer AJCC V7 Stage I Gastric Cancer AJCC V7 Stage I Lung Cancer AJCC v7 Stage I Ovarian Cancer AJCC v6 and v7 Stage I Pancreatic Cancer AJCC v6 and v7 Stage I Prostate Cancer AJCC v7 Stage I Uterine Corpus Cancer AJCC v7 Stage II Bladder Cancer AJCC v6 and v7 Stage II Breast Cancer AJCC v6 and v7 Stage II Colorectal Cancer AJCC v7 Stage II Esophageal Cancer AJCC v7 Stage II Gastric Cancer AJCC v7 Stage II Lung Cancer AJCC v7 Stage II Ovarian Cancer AJCC v6 and v7 Stage II Pancreatic Cancer AJCC v6 and v7 Stage II Prostate Cancer AJCC v7 Stage II Uterine Corpus Cancer AJCC v7 Stage III Bladder Cancer AJCC v6 and v7 Stage III Breast Cancer AJCC v7 Stage III Colorectal Cancer AJCC v7 Stage III Esophageal Cancer AJCC v7 Stage III Gastric Cancer AJCC v7 Stage III Lung Cancer AJCC v7 Stage III Ovarian Cancer AJCC v6 and v7 Stage III Pancreatic Cancer AJCC v6 and v7 Stage III Prostate Cancer AJCC v7 Stage III Uterine Corpus Cancer AJCC v7 Stage IV Bladder Cancer AJCC v7 Stage IV Breast Cancer AJCC v6 and v7 Stage IV Colorectal Cancer AJCC v7 Stage IV Esophageal Cancer AJCC v7 Stage IV Gastric Cancer AJCC v7 Stage IV Lung Cancer AJCC v7 Stage IV Ovarian Cancer AJCC v6 and v7 Stage IV Pancreatic Cancer AJCC v6 and v7 Stage IV Prostate Cancer AJCC v7 Stage IV Uterine Corpus Cancer AJCC v7 Thyroid Gland Carcinoma Other: Questionnaire Administration Procedure: Biospecimen Collection

Detailed Description:

PRIMARY OBJECTIVE:

I. To provide a blinded reference set of cancer versus (vs.) non-cancer blood samples that will be used to validate assays for inclusion in a prospective clinical trial focused on utility of blood-based multi-cancer early detection.

SECONDARY OBJECTIVES:

I. Evaluate test performance at the time of initial cancer diagnosis by tumor type.

II. Evaluate test performance at the time of initial cancer diagnosis by clinical stage.

OUTLINE:

Participants complete a questionnaire at baseline. Participants undergo collection of blood samples at registration and at 12 months after registration. Patients with a cancer diagnosis may undergo collection of tissue samples at registration and 12 months after registration.

After completion of study, participants are followed up at 1 year.

Study Design
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Study Type : Observational
Estimated Enrollment : 2000 participants
Observational Model: Case-Control
Time Perspective: Prospective
Official Title: Blinded Reference Set for Multicancer Early Detection Blood Tests
Actual Study Start Date : August 1, 2022
Estimated Primary Completion Date : January 31, 2025
Estimated Study Completion Date : February 2025

Resource links provided by the National Library of Medicine


Groups and Cohorts
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Group/Cohort Intervention/treatment
Screening (questionnaire, biospecimen collection)
Participants complete a questionnaire at baseline. Participants undergo collection of blood samples at registration and at 12 months after registration. Patients with a cancer diagnosis may undergo collection of tissue samples at registration and 12 months after registration.
 Other: Questionnaire Administration
Complete questionnaire

Procedure: Biospecimen Collection
Undergo collection of tissue and blood samples


Outcome Measures
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Primary Outcome Measures :
  1. Provision of blinded reference set of cancer versus non-cancer blood samples [ Time Frame: Up to 1 year ]
    Diagnostic ability will be assessed across the entire cohort of 2000 subjects by estimating the sensitivity and specificity with 95% confidence intervals.


Secondary Outcome Measures :
  1. Test performance at the time of initial cancer diagnosis by tumor type [ Time Frame: Up to 1 year ]
    Diagnostic ability is assessed within each cancer type and within each cancer type and stage combination by estimating the sensitivity and specificity with 95% confidence intervals. The width of these confidence intervals will vary by sample size and the sensitivity and specificity rates.

  2. Test performance at the time of initial cancer diagnosis by clinical stage [ Time Frame: Up to 1 year ]
    Diagnostic ability is assessed within each cancer stage and within each cancer type and stage combination by estimating the sensitivity and specificity with 95% confidence intervals. The width of these confidence intervals will vary by sample size and the sensitivity and specificity rates.


Biospecimen Retention:   Samples With DNA
Blood, tissue

Eligibility Criteria
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Ages Eligible for Study:   40 Years to 75 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population
Patients with a cancer diagnosis and participants without cancer and without suspicion of cancer and with a high suspicion of cancer
Criteria

Inclusion Criteria:

  • Participants with a cancer diagnosis: Documentation of disease:

    • Histologic documentation: Histologically confirmed diagnosis of invasive cancer

    • Stage: Stage I-IV per American Joint Committee on Cancer (AJCC) 7th edition, with the exception of patients with leukemia, lymphoma, and multiple myeloma

      • For leukemia: Type (chronic lymphocytic leukemia [CLL], chronic myeloid leukemia [CML], acute lymphoblastic lymphoma [ALL], acute myeloid leukemia [AML])
      • For lymphoma: Stage I-IV based on Ann Arbor staging
      • For multiple myeloma: Stage I, II, III based on Revised International Staging System (RISS)

    • One of the following tumor types:

      • Colorectal
      • Bladder
      • Head and neck
      • Hepatobiliary
      • Lung
      • Lymphoma
      • Leukemia
      • Ovary *** For these specific cancer types only, patients may be enrolled prior to histologic confirmation of malignancy. Sites are required to contact the study chairs to review appropriateness for enrollment
      • Pancreas *** For these specific cancer types only, patients may be enrolled prior to histologic confirmation of malignancy. Sites are required to contact the study chairs to review appropriateness for enrollment
      • Multiple myeloma
      • Gastric, esophageal or gastroesophageal
      • Breast
      • Thyroid

      • Kidney

        • For these specific cancer types only, patients may be enrolled prior to histologic confirmation of malignancy. Sites are required to contact the study chairs to review appropriateness for enrollment
      • Endometrium
      • Prostate

      • Melanoma

        *** For these specific cancer types only, patients may be enrolled prior to histologic confirmation of malignancy. Sites are required to contact the study chairs to review appropriateness for enrollment

      • Sarcoma
  • Participants with a cancer diagnosis: No prior definitive systemic or local anti-cancer intervention
  • Participants with a cancer diagnosis: Age >= 40 and =< 75
  • Participants with a cancer diagnosis: No known current pregnancy by self-report
  • Participants with a cancer diagnosis: No known or prior history of in situ or invasive malignancy (excluding in situ non-melanoma skin cancers) other than the current cancer diagnosis
  • Participants with a cancer diagnosis: Willingness to provide blood samples for research use
  • Participants with a cancer diagnosis: Absence of medical contraindications to a research blood draw volume of 60 mL
  • Participants with a cancer diagnosis: No history of organ transplantation

  • Participants with a cancer diagnosis: Ability to read and comprehend English or Spanish

    * Eligibility is restricted to individuals who can comprehend and read English or Spanish given that participation in the study will require the ability to read and complete questionnaires that are available only in those two languages

  • Participants without a cancer diagnosis and without suspicion of cancer: Age >= 40 and =< 75
  • Participants without a cancer diagnosis and without suspicion of cancer: No known current pregnancy by self-report
  • Participants without a cancer diagnosis and without suspicion of cancer: No known or prior history of in situ or invasive malignancy (excluding in situ non-melanoma skin cancers)
  • Participants without a cancer diagnosis and without suspicion of cancer: Willingness to provide blood samples for research use
  • Participants without a cancer diagnosis and without suspicion of cancer: Absence of medical contraindications to a research blood draw volume of 60 mL
  • Participants without a cancer diagnosis and without suspicion of cancer: No history of organ transplantation

  • Participants without a cancer diagnosis and without suspicion of cancer: Ability to read and comprehend English or Spanish

    * Eligibility is restricted to individuals who can comprehend and read English or Spanish given that participation in the study will require the ability to read and complete questionnaires that are available only in those two languages

  • Participants with a high suspicion of cancer: High suspicion of ovarian cancer, pancreatic cancer, kidney cancer, or melanoma by clinical and/or radiological assessment, with plans for histologic or cytologic confirmation within 28 days after study blood draw

    * Examples of highly suspicious cases include: elevated CA125 and abnormal transvaginal ultrasound, suspicious renal or pancreatic mass on imaging, suspicious cutaneous lesion concerning for melanoma

  • Participants with a high suspicion of cancer: Central review of radiology reports and/or clinical documentation conducted by study chairs
  • Participants with a high suspicion of cancer: Age >= 40 and =< 75
  • Participants with a high suspicion of cancer: No known current pregnancy by self-report
  • Participants with a high suspicion of cancer: No known or prior history of in situ or invasive malignancy (excluding in situ non-melanoma skin cancers) other than the current cancer diagnosis
  • Participants with a high suspicion of cancer: Willingness to provide blood samples for research use
  • Participants with a high suspicion of cancer: Absence of medical contraindications to a research blood draw volume of 60 mL
  • Participants with a high suspicion of cancer: No history or organ transplantation
  • Participants with a high suspicion of cancer: Ability to read and comprehend English or Spanish * Eligibility is restricted to individuals who can comprehend and read English and Spanish given that participation in the study will require the ability to read and complete questionnaires that are available only in those two languages
Contacts and Locations
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Top of Page Study Description Study Design Groups and Cohorts Outcome Measures Eligibility Criteria Contacts and Locations More Information

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT05334069


Contacts
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Contact: Marie Wood, MD (720) 848-0300 marie.wood@cuanschutz.edu

Locations
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Sponsors and Collaborators
Alliance for Clinical Trials in Oncology
National Cancer Institute (NCI)
Investigators
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Study Chair: Marie Wood, MD University of Colorado, Denver
More Information
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Responsible Party: Alliance for Clinical Trials in Oncology
ClinicalTrials.gov Identifier: NCT05334069    
Other Study ID Numbers: A212102
NCI-2022-02477 ( Registry Identifier: NCI Clinical Trial Reporting Program )
UG1CA189823 ( U.S. NIH Grant/Contract )
First Posted: April 19, 2022    Key Record Dates
Last Update Posted: March 17, 2023
Last Verified: March 2023

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Additional relevant MeSH terms:
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Blood Protein Disorders
Lymphoma
Carcinoma
Breast Neoplasms
Leukemia
Lung Neoplasms
Prostatic Neoplasms
Neoplasms
Colorectal Neoplasms
Leukemia, Myeloid
Multiple Myeloma
Neoplasms, Plasma Cell
Pancreatic Neoplasms
Ovarian Neoplasms
Carcinoma, Ovarian Epithelial
 Stomach Neoplasms
Precursor Cell Lymphoblastic Leukemia-Lymphoma
Leukemia, Lymphocytic, Chronic, B-Cell
Urinary Bladder Neoplasms
Esophageal Neoplasms
Leukemia, Myelogenous, Chronic, BCR-ABL Positive
Thyroid Neoplasms
Carcinoma, Renal Cell
Kidney Neoplasms
Neoplasms by Histologic Type
Lymphoproliferative Disorders
Lymphatic Diseases
Immunoproliferative Disorders
Immune System Diseases
Neoplasms, Glandular and Epithelial