PERformance of Multi-Cancer Early-detectIon Based on Various Biomarkers in fEmale Cancers, PERCEIVE-II

Fudan University

Status

Enrolling

Conditions

Gynecologic Cancer

Study type

Observational

Funder types

Other

Industry

Identifiers

NCT06001099

RSCD2021002

Details and patient eligibility

About

This study is a prospective study aimed to validate the performance of combined multi-omitcs assays for early detection of gynecologic cancers. Biomarkers of cfDNA methylation, ctDNA mutation and blood miRNA markers will be evaluated. The study will enroll approximately 2935 female participants, including participants with gynecologic cancers patients and healthy participants.

Enrollment

2,935 estimated patients

Sex

Female

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria for Cancer Arm Participants:

Age 18 years or older
Able to provide a written informed consent
Confirmed diagnosis or highly suspicious cases of gynecologic malignancies within 42 days prior to blood collection
No prior or ongoing anti-cancer therapy (local or systematic) prior to study blood draw

Exclusion Criteria for Cancer Arm Participants:

Pregnancy or lactating women
Recipients of organ transplant or prior non-autologous (allogeneic) bone marrow transplant or stem cell transplant
Recipients of blood transfusion within 7 days prior to study blood draw
Recipients of any anti-cancer therapy within 30 days prior to study blood draw, due to diseases other than cancer.
previous history of malignant tumor;
precancerous lesions or benign diseases confirmed by biopsy or surgical specimen;
unknown or insufficient to determine the nature of the lesion by histopathological reports;

Inclusion Criteria for healthy control Arm Participants:

Able to provide a written informed consent.
Able to provide sufficient and qualified blood samples for study tests.
No cancer related symptoms within 30 days prior to study screening.
Cancer history with curative treatment completed over 3 years without recurrence prior to study enrollment.

Exclusion Criteria for healthy control Arm Participants:

Insufficient qualified blood sample for study test.
During pregnancy or lactation.
Recipient of organ transplant or prior non-autologous (allogeneic) bone marrow or stem cell transplant.
Recipient of blood transfusion within 30 days prior to study blood draw.
Recipient of anti-infectious therapy within 14 days prior to study blood draw.
Have received or are undergoing curative cancer treatment within three years prior to study screening.
With autoimmune or other diseases with severe comorbidities.