The goal of this observational study is to screen and differentiate common cancers in participants with or without suspicious lesions. The main question the investigators aim to answer is: Can the developed model, using peripheral blood cell-free DNA sequencing, work well in screening and classifying common cancers especially in the early stages? Participants will undergo the collection of 15\~20ml of blood and 1\~2 telephone follow-up calls.
Study Type
OBSERVATIONAL
Enrollment
3,200
Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University
Guangzhou, Guangdong, China
NOT_YET_RECRUITINGThe First Affiliated Hospital of Guangzhou Medical University
Guangzhou, Guangdong, China
RECRUITINGFirst Hospital of China Medical University
Shenyang, Liaoning, China
NOT_YET_RECRUITINGPeople's Hospital of Ningxia Hui Autonomous Region
Yinchuan, Ningxia, China
NOT_YET_RECRUITINGFirst Affiliated Hospital of Air Force Military Medical University
Xi'an, Shaanxi, China
RECRUITINGTang-du Hospital
Xi'an, Shaanxi, China
RECRUITINGGuanxian People's Hospital
Liaocheng, Shandong, China
RECRUITINGAffiliated Cancer Hospital of Xinjiang Medical University
Ürümqi, China
RECRUITINGdiagnostic accuracy
This refers to the ability of the test (peripheral blood cell-free DNA sequencing) to correctly classify individuals into the categories of having or not having the disease. It is a measure of the test's overall effectiveness. The reference test is histological test for cancers or one-year follow-up for non-cancers.
Time frame: Immediately after test completion
sensitivity
This is the ability of the test (peripheral blood cell-free DNA sequencing) to correctly identify those with the disease. It is the proportion of true positive results (those with the disease who test positive) to the total number of individuals who actually have the disease. The reference test is histological test for cancers or one-year follow-up for non-cancers.
Time frame: Immediately after test completion
specificity
This is the ability of the test (peripheral blood cell-free DNA sequencing) to correctly identify those without disease. It is the proportion of true negative results (those without the disease who test negative) to the total number of individuals who actually do not have the disease. The reference test is histological test for cancers or one-year follow-up for non-cancers.
Time frame: Immediately after test completion
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