A Prospective Study of Expression Profiling-based Assessment of the Efficacy of Neoadjuvant Therapy for Rectal Cancer
NCT ID: NCT06746298
Last Updated: 2024-12-24
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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NOT_YET_RECRUITING
118 participants
OBSERVATIONAL
2025-01-01
2027-05-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Rectal cancer patients receiving neoadjuvant therapy
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Patients with rectal adenocarcinoma diagnosed by colonoscopic biopsy
* Neoadjuvant therapy according to guideline recommendations
* Endoscopic biopsy with access to biopsy tissue for subsequent RNA-seq testing
* Patients who do not have a combination of primary malignant tumors elsewhere.
* Patients who understand the purpose of the trial, participate voluntarily and sign an informed consent form.
Exclusion Criteria
* Sample does not meet the requirements for subsequent RNA-seq testing
* Cases enrolled with a subsequent diagnosis other than rectal adenocarcinoma.
* The patient refuses or is unable to complete the entire neoadjuvant treatment
* Lack of post-neoadjuvant imaging results and lack of routine postoperative pathology results.
* Other patients who, in the judgment of the investigator, do not meet the enrollment requirements
18 Years
ALL
No
Sponsors
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Shanghai Minimally Invasive Surgery Center
OTHER
Responsible Party
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Central Contacts
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Other Identifiers
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RNA-seq-Neo
Identifier Type: -
Identifier Source: org_study_id