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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05202314
Other study ID # 2021-12-24
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date December 12, 2021
Est. completion date December 30, 2026

Study information

Verified date February 2023
Source Beijing Chao Yang Hospital
Contact Jia Gang Han, MD
Phone +861085231604
Email hjg211@163.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Patients with obstruction are associated with worse oncologic outcomes compared with those having nonobstructive tumors. Conventionally, patients with malignant large bowel obstruction receive emergency surgery, with morbidity rates of 30%-60% and mortality rates of 7-22%, and about two-thirds of such patients end up with a permanent stoma. Self-expanding metallic stents (SEMS) haven been used as a bridge to surgery (to relieve obstruction prior to elective surgery) in patients with potentially resectable colorectal cancer. Several clinical trials demonstrate that SEMS as a bridge to surgery may be superior to emergency surgery considering the short-term outcomes. SEMS is associated with lower morbidity and mortality rate, increased primary anastomosis rate, and decreased stoma creation rate. Although about half of patients can achieve primary anastomosis after stent placement, the primary anastomosis rate is still significantly lower compared with nonobstructing elective surgery. The interval between stent placement and surgery may be not long enough that bowel decompression is insufficient at the time of operation. Furthermore#the long-term oncologic results regarding SEMS as a bridge to surgery are still limited and contradictory. Sabbagh et al. suggest worse overall survival of patients with SEMS insertion compared with emergency surgery, the 5-year cancer-specific mortality was significantly higher in the SEMS group (48% vs 21%, respectively, P=0.02). One interpretation is that tumor cells may disseminate during the procedure of colonic stenting placement. Immunotherapy has proven to be highly effective as first-line treatment of metastatic colorectal cancer (CRC). And immunotherapy also has emerged as a neoadjuvant approach, possibly changing treatment strategy for both primary resectable and metastatic CRC. We hypothesis that, regardless of the MSI state, immunotherapy (Camrelizumab, an anti-PD-1 antibody) combined with chemotherapy after stenting may improve overall survival by eradicating micrometastasis. Moreover, immunotherapy (Camrelizumab, an anti-PD-1 antibody) combined with neoadjuvant chemotherapy prolongs the interval between stent placement and surgery, and the time for bowel decompression is more sufficient, which may increase the success rate of primary anastomosis and decrease risk of stoma formation, and furthermore, improve OS and PFS.


Description:

We hypothesis that, regardless of the MSI state, immunotherapy combined with immediate chemotherapy after stenting may improve overall survival by eradicating micrometastasis. Moreover, immunotherapy (Camrelizumab, an anti-PD-1 antibody) combined with neoadjuvant chemotherapy prolongs the interval between stent placement and surgery, and the time for bowel decompression is more sufficient, which may increase the success rate of primary anastomosis and decrease risk of stoma formation, and furthermore, improve OS and PFS.


Recruitment information / eligibility

Status Recruiting
Enrollment 20
Est. completion date December 30, 2026
Est. primary completion date December 30, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: - Radiologically proven colonic obstruction of the left colon/upper rectum presumed secondary to a carcinoma - Able to give written, informed consent - Primary tumor was resectable - ECOG score 0 or 1 - Haemoglobin greater than 100 g/L after transfusion before chemotherapy, - White blood cells greater than 3.0×10# /L - Platelets greater than 100×10# / L; - Glomerular filtration rate greater than 50 mL per minute as calculated by the Wright or Cockroft formula - Bilirubin less than 1.5×Upper Limit of Normal(ULN) - ALT and AST less than 2.5×ULN Exclusion Criteria: - Distal rectal cancers(equal or less than 10cm from the anal verge) - Patients with signs of peritonitis and/or bowel perforation - Patients who did not give informed consent - Patients who were considered unfit for operative treatment or refuse surgery. - Patients with suspected or proven metastatic adenocarcinoma; - Patients with unresectable colorectal cancer, or planning for palliative treatment.

Study Design


Intervention

Drug:
Immunotherapy (Camrelizumab)
After clinical success of colonic stenting, regardless of the MSI state, patients will receive Immunotherapy (Camrelizumab 200mg) for 2 cycles compined with neoadjuvant chemotherapy with mFOLFOX6 regimen for 3 cycles or CapeOx regimen for 2 cycles. Patients will undergo surgery 2-3 weeks after the last cycle chemotherapy

Locations

Country Name City State
China Beijing Chaoyang Hospital, Capital Medical University Beijing Beijing

Sponsors (1)

Lead Sponsor Collaborator
Beijing Chao Yang Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Pathological complete remission No tumor cell found in surgical specimens 2 weeks after patients received radical operation
Secondary Disease Free Survival No tumor regrowth or recurrence or metastasis found 3 years after operation
Secondary Overall Survival Survive during following 3 years after operation
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