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Radiosensitivity study for rectal cancer based on genomics and imaging

Radiosensitivity study for rectal cancer based on genomics and imaging

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900021763
Enrollment
Unknown
Registered
2019-03-08
Start date
2020-01-01
Completion date
Unknown
Last updated
2019-03-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Rectal Cancer

Interventions

Radiotherapy group:PDX model radiotherapy treatment
Radiotherapy and chemotherapy group:PDX model radiotherapy and chemotherapy treatment
Control group:PDX modeling

Sponsors

Shanghai Oriental Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Untreated primary rectal cancer patients diagnosed by histopathological examination; 2. Patients who meet the requirements of preoperative neoadjuvant chemoradiotherapy for rectal cancer and undergo preoperative chemoradiotherapy for colon cancer as planne; 3. Objective tumors that meet RECIST 1.1 criteria and can be evaluated by CT/MRI; 4. KPS score = 60, expected survival time = 3 months; 5. The patient voluntarily signed the informed consent form, with good compliance.

Exclusion criteria

Exclusion criteria: 1. Patients with incomplete clinical data; 2. Those who have not undergone surgery or have unplanned reoperations after surgery; 3. The patient was found to have a second tumor during the treatment and interfered with the study.

Design outcomes

Primary

MeasureTime frame
Overall survival;Disease free survival;Recurrence rate;

Secondary

MeasureTime frame
Pathologic complete response;Anal protection rate;Tumor downgrade rate;Adverse reactions;Postoperative complications;NGS;

Countries

China

Contacts

Public ContactChuangang Fu

Shanghai Oriental Hospital

fugang416@126.com+86 13817334288

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026