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Investigation of a Novel Blood Test to Identify Breast Cancer (IDBC)

Status: Recruiting
Location: See all (4) locations...
Intervention Type: Diagnostic test
Study Type: Observational
SUMMARY

Detecting cancer as early as possible is key to achieving positive outcomes in response to diagnosis and treatment. The current project is aimed at validating a novel blood-based breast cancer identification test (Syantra DX Breast Cancer) that has been developed by Syantra Inc. Syantra DX Breast Cancer measures gene expression signatures in whole blood, and has been retrospectively demonstrated in 780 samples. The test uses proprietary algorithms to analyse gene expression characteristics from a novel multi-biomarker panel, and then classify a sample as positive or negative for breast cancer. Based upon test performance in a retrospective environment, a prospective validation study is being proposed. The primary objective of this study is to validate Syantra DX Breast Cancer methodology and biomarker panel using prospective samples, well categorized by diagnostic imaging scores, pathology outcomes, and subject characteristics.

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 30
Maximum Age: 75
Healthy Volunteers: t
View:

• Aged 30-75 years

• Normal breast examination - No cancer detected/suspected by physical exam, diagnostic radiology or screening mammography

• Women with suspected Invasive Breast Cancer

• Individuals with an abnormal or suspicious mammogram

• Abnormal screening mammogram with suspected benign breast disease or proliferative changes

Locations
Other Locations
Canada
Alberta Cancer Research Biobank
RECRUITING
Calgary
Republic of Korea
Severance Hospital
COMPLETED
Soeul
United Kingdom
North Manchester General Hospital
RECRUITING
Manchester
Wythenshawe Hospital, Southmoor Road
RECRUITING
Manchester
Contact Information
Primary
Natasha Jones
Natasha.Jones@mft.nhs.uk
0161 291 4045
Backup
Linda Bailey
linda.bailey3@mft.nhs.uk
0161 291 4492
Time Frame
Start Date: 2019-01-24
Estimated Completion Date: 2032-12-31
Participants
Target number of participants: 10000
Treatments
Investigational Population
Suspected Invasive Breast Cancer (any size) or DCIS (pre-invasive) are of particular interest. Women with abnormal screening mammograms (R3-5) recalled for further investigation.~Inclusion criteria~* Women with suspected Invasive Breast Cancer (tumours of any size and/or DCIS).~* Individuals with an abnormal or suspicious screening mammogram recalled for further evaluation.~* Suspected Invasive Breast Cancer (tumours of any size and/or DCIS).~* Willing to give written Informed Consent and provide whole blood samples~* Age 30-75 years~Exclusion criteria~* Breast surgery within the previous 12 months (for any reason) or recent breast biopsy (including needle core biopsy)~* Inoperable (T4 category) or inflammatory breast cancer~* Previous history of cancer previously at any site~* Previous history of breast cancer~* Concomitant or other concurrent anti-cancer therapy~* Male~* Existing cancer diagnosis
Borderline (Atypica and LCIS) Population
Women with borderline pathological B3 lesions (suspected atypia Ductal or Lobular and benign proliferative disease without DCIS or invasion) Inclusion criteria~* Abnormal screening mammogram with suspected benign breast disease or proliferative changes~* Willing to give Written Informed Consent and provide whole blood samples~* Aged 30-75 years~Exclusion criteria~* Existing cancer diagnosis~* Male~* Breast surgery within the previous 12 months (for any reason) or recent breast biopsy (including needle core biopsy)~* Previous history of any cancer~* Previous history of breast cancer~* Concomitant or other concurrent anti-cancer therapy
Control Population
Healthy Controls Inclusion criteria~* Normal breast examination - No cancer detected/suspected by physical exam, diagnostic radiology or screening mammography~* Willing to give Written Informed Consent and provide whole blood samples~* Aged 30-75 years~Exclusion criteria~* Cancer diagnosis~* Male~* Breast surgery within the previous 12 months (for any reason) or recent breast biopsy (including needle core biopsy)~* Previous history of any cancer~* Concomitant or other concurrent anti-cancer therapy
Related Therapeutic Areas
Sponsors
Leads: Syantra Inc.
Collaborators: University of Calgary

This content was sourced from clinicaltrials.gov