Novel Serum Markers for Monitoring Response to Anti-Cancer Therapy

NCT ID: NCT00349830

Last Updated: 2025-01-28

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Total Enrollment

2000 participants

Study Classification

OBSERVATIONAL

Study Start Date

2002-01-31

Study Completion Date

2032-01-31

Brief Summary

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The purpose of this study is to measure the levels of serum proteins and other biomarkers in cancer patients and in patients suspected of having cancer. We believe that some of these markers may be useful for confirming the diagnosis or for selecting patients for specific types of cancer therapies. These markers may also help to predict response to therapy, relapse after therapy, and survival after therapy.

Detailed Description

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This is a blood serum collection study at Stanford University for patients with cancer at a variety of disease sites. The purpose of this study is to collect and store blood serum from patients before, during, and after anti-cancer therapy to find new biomarkers that signal disease or response to anti-cancer therapy. The collection and analysis of these biomarkers may lead to improved diagnostic and treatment therapies for certain cancers in the future. We are also interested in collecting blood serum from healthy individuals such as the spouses, relatives, and friends of cancer patients to obtain healthy controls for comparison

Conditions

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Carcinomas (Including Squamous Cell and Adenocarcinoma) Neoplasms

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Interventions

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blood draw

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

1. Age \> or = 18; for the samples collected under the NIH grant, no subjects below the age of 20 will be enrolled.
2. Prior diagnosis of cancer or suspected of having cancer
3. Karnofsky performance status of greater than 70
4. Standard pretreatment evaluation
5. Signed Stanford University Human Subjects Committee consent
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Stanford University

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Maximilian Diehn

Role: PRINCIPAL_INVESTIGATOR

Stanford University

Locations

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Stanford University School of Medicine

Stanford, California, United States

Site Status RECRUITING

Countries

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United States

Central Contacts

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[email protected]

Role: CONTACT

650-498-7757

Facility Contacts

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Rene Bonilla

Role: primary

650-498-7703

Other Identifiers

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IRB-13535

Identifier Type: -

Identifier Source: org_study_id

77923

Identifier Type: OTHER

Identifier Source: secondary_id

IRB-13535

Identifier Type: OTHER

Identifier Source: secondary_id

VAR0006

Identifier Type: OTHER

Identifier Source: secondary_id

5R01CA18829804

Identifier Type: OTHER_GRANT

Identifier Source: secondary_id

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