About this trial
Among the currently important biomarkers, circulating tumor cells and microRNA (miRNA) have received significant attention. The latter, also translated as micro-ribonucleic acid, is a widely present ribonucleic acid (RNA) molecule in eukaryotes, approximately 21 to 23 nucleotides in length, which regulates the expression of other genes. miRNAs originate from RNAs that are transcribed from DNA but cannot be further translated into proteins (classified as non-coding RNA). miRNAs bind to target messenger RNA (mRNA), thereby inhibiting post-transcriptional gene expression, and play important roles in regulating gene expression, the cell cycle, and the timing of biological development.The project will recruit 300 subjects who have been diagnosed with cancer by a physician and for whom the decision has been made to use immunotherapy. Blood samples will be collected before and after treatment (past pathological diagnostic tissues may also be reviewed as required for the study). The study will analyze the differences in the quantity of free microRNAs, the number of circulating tumor cells, and the differences in surface antigen expression in the subjects' blood, as well as the specific surface antigen expression status in the cancer tissues, and perform statistical analysis.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Aged above 20 years.
A patient diagnosed with cancer with immunotherapy
Competent to give informed consent and agree to join the study.
Disqualifiers
Aged < 20 years.
Refuse to join the study
Trial population
The most crucial factor in preventing death for cancer patients is early diagnosis and the detection of recurrence.The project will recruit 300 subjects who have been diagnosed with cancer by a physician and for whom the decision has been made to use immunotherapy. Blood samples will be collected before and after treatment. The study will analyze the differences in the quantity of free microRNAs, the number of circulating tumor cells, and the differences in surface antigen expression in the subjects' blood, as well as the specific surface antigen expression status in the cancer tissues, and perform statistical analysis
Trial design
Case-control
Prospective
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
counting of Circulating Tumor Cells
The study will do the counting of circulating tumor cells in the participants with immunotherapy.
counting of Circulating Tumor Cells
The study will do the counting of circulating tumor cells in the participants with immunotherapy.
counting of Circulating Tumor Cells
The study will do the counting of circulating tumor cells in the participants with immunotherapy.
Secondary outcomes
microRNAs sequence
The study will analyze the differences in the quantity of free microRNAs
microRNAs sequence
The study will analyze the differences in the quantity of free microRNAs
microRNAs sequence
The study will analyze the differences in the quantity of free microRNAs
Other outcomes
Treatment response
Record the response after immuntherapy
Treatment response
Record the response after immuntherapy
Sponsors and contacts
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