NCT04833387Active, not recruitingPhase 2
PD-1 Antibody Following Preoperative Chemoradiotherapy for Locally Advanced pMMR/MSS Rectal Cancer
PD-1 Antibody as a Sequential Therapy Following Preoperative Chemoradiotherapy for Locally Advanced pMMR/MSS Rectal Cancer: an Open, Multi-center, Phase II Clinical Trial
Source: ClinicalTrials.gov · Last updated 11 Jan 2023
Brief summary (registry, in English)
In this open-label phase II study, patients will be scheduled for neoadjuvant treatment with PD-1 antibody following preoperative Chemoradiotherapy with capecitabine for pMMR/MSS rectal cancer staged as locally advanced (cT3-T4N+/-M0 for rectal cancer). This treatment will be given during the window period until surgical resection of the tumor.
- Status (registry)
- Active, not recruiting
- Phase (registry)
- Phase 2
- Study type
- Interventional
- Enrollment
- 30 (estimated)
- First submitted
- 4 Apr 2021
- Start date
- 1 Jan 2021
- Primary completion date
- 31 Dec 2024
- Lead sponsor
- Sun Yat-sen University
- Diseases
- Colorectal cancer
- NCT number
- NCT04833387
What you commit to
- Study type: Interventional · Phase 2
- Planned participants: 30
- From 1 Jan 2021 to the primary completion date, 31 Dec 2024
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- There is evidence that there is distant metastasis before surgery;
Other illness
- Rectal cancer with unstable microsatellite (MSI or dMMR);
- Known history of human immunodeficiency virus (HIV) or chronic hepatitis B or C (high copy viral DNA);
- Autoimmune diseases;
- Other active clinical serious infections (\>NCI-CTC version 3.0);
- Have a history of pelvic or abdominal radiotherapy;
- Multiple primary cancers;
- Patients who need treatment for seizures (such as steroids or anti-epileptic treatment);
- Have a known additional malignant tumors within 5 years. Exceptions include basal cell carcinoma of the skin that has undergone potentially curative therapy or in situ cervical cancer;
- Chronic inflammatory bowel disease, intestinal obstruction;
- Drug abuse and medical, psychological or social conditions may interfere with patients' participation in research or have an impact on the evaluation of research results;
- Known or suspected to be allergic to the study drug or to any drug given in connection with this test;
- Any unstable conditions or situations that may endanger patient safety and compliance
Other
- Preoperative biopsy of tumor immunohistochemistry TPS≤1% or CPS≤1
- Patients in clinical phase I;
- Cachexia, decompensation of organ function;
Who the study is looking for
- Patients who personally provided written consent for participation in the study
- Treatment-naive patients with rectal cancer, in whom the inferior margin of the tumor was at a distance of 12 cm or less from the AV before CRT
- Primary rectal cancer histopathologically confirmed to be adenocarcinoma
- Clinical stage of T3,and T4 ,N any,M0,before CRT
- Macroscopic radical resection could be feasible, based on diagnostic imaging before CRT
- Patients with the ECOG performance status of 0 or 1 at the time of enrollment
- Patients without distant metastasis on the imaging test before CRT
- Preoperative biopsy of tumor immunohistochemistry TPS\>1% or CPS\>1
- Life expectancy of greater than 2 years
- No signs of intestinal obstruction; or the obstruction has been relieved after the proximal colostomy operation
- Hematology: WBC\>4000/mm3; PLT\>100000/mm3; Hb\>10g/dL
- Liver function: SGOT and SGPT are less than 1.5 times the normal value; bilirubin is less than 1.5mg/dL
- Renal function: creatinine \<1.8mg/dL Others: non-pregnant or breast-feeding women; no other malignant diseases (except for non-melanoma or cervical carcinoma in situ) within 5 years or during the same period; no mental illness that causes the inability to obtain informed consent; no other serious diseases that can shorten the survival time disease.
- Have not received rectal surgery in the past;
- Have not received chemotherapy or radiotherapy in the past;
- Have not received biological treatment in the past;
- Past endocrine therapy: unlimited.
Age in the registry: 18 years to 75 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| 651 Dongfeng Road East Coordinator of this site? Confirm its status | Guangzhou | China | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.