NCT02934360UnknownNot Applicable
Evaluation of the TR(ACE) Assay for the Ability to Aid in Monitoring Disease Progress, Response to Therapy or for Recurrent or Residual Disease for Patients With Previously Diagnosed Cancers (Stage III and IV Lung and Stage IV Breast)
Biological Dynamics16 sites in 1 country450 target enrollmentStarted: September 2016Last updated:
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Sponsor
- Enrollment
- 450
- Locations
- 16
- Primary Endpoint
- Clinical Assessment change
Study Overview
Brief Summary
The TR(ACE) Assay is a quantitative in vitro diagnostic test run on the TR(ACE) Instrument intended for the measurement of high molecular weight human DNA from plasma as an aid to monitoring disease progression or response to therapy or recurrent or residual disease.
Detailed Description
This study is to establish the clinical performance of the TR(ACE) Assay. Deltas of serial TR(ACE) Assay measurements will be compared to the standard of care physician clinical assessment and RECIST 1.1 criteria evaluation relative to the previous visit. Significant changes in serial TR(ACE) Assay measurements are hypothesized to correlate with disease progression or response.
Study Design
- Study Type
- Observational
- Observational Model
- Cohort
- Time Perspective
- Prospective
Eligibility Criteria
- Ages
- 21 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Non-small cell lung: Male or Female Adult patient >= 21 years old
- •Breast only: Female Adult patient >= 21 years old
- •Previously diagnosed with one of the following cancers:
- •Breast or Non-small Cell Lung
- •Cancer has progressed to at least Stage III or higher for lung cancer or,
- •Cancer has progressed to stage IV (metastatic) breast cancer
- •Participating in standard of care cancer therapy requiring frequent treatments, typically intravenous chemotherapy visits (or as determined by the standard of care for the particular cancer assessed), of a minimum of three (3) treatment visits planned in 9 months from date of enrollment where a clinical assessment will be conducted
Exclusion Criteria
- •Physician assessment that obtaining two extra whole blood specimens with minimum volume of 5 mL per treatment visit is contraindicated
- •Stage I and II Non-small Cell Lung Cancer
- •Stage I through III breast cancer
- •Pregnant or planning to become pregnant during the course of the study
- •Unable to obtain informed consent from subject or their legal representative
- •Life expectancy is less than 9 months
- •Presence of one or more of the following other chronic diseases
- •Another type of cancer except for non-melanomatous skin tumors
- •Autoimmune disease requiring DMARDS or Biologics
- •Infectious disease requiring prolonged intravenous antibiotics or hospitalization
- •Renal disease specifically those in End Stage Renal Failure
- •Recent (< 3 weeks) major trauma or major surgical procedure(s) or radiation therapy prior to enrollment in the study
- •Recent (< 2 months) major occlusive arterial event such as MI or CVA prior to enrollment in the study
Outcomes
Primary Outcomes
Clinical Assessment change
Time Frame: Standard of care (approximately every 6 weeks to 3 months) for 6- 9 months
Standard of care physician's clinical assessment of disease progression or response compared to previous visit
Secondary Outcomes
- RECIST 1.1 criteria(Standard of care (approximately every 6 weeks to 3 months) for 6- 9 months)
Investigators
Study Sites (16)
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