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NCT05202314Recruiting

Camrelizumab Combined With Neoadjuvant Chemotherapy After Stent Placement for Left-Sided Obstructive Colonic Cancer

Camrelizumab Combined With Neoadjuvant Chemotherapy After Stent Placement Versus Surgery Alone for Left-Sided Obstructive Colonic Cancer

Source: ClinicalTrials.gov · Last updated 21 Feb 2023 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

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.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
20 (estimated)
First submitted
10 Jan 2022
Start date
12 Dec 2021
Primary completion date
30 Dec 2023
Lead sponsor
Beijing Chao Yang Hospital
NCT number
NCT05202314

What you commit to

  • Study type: Interventional
  • Planned participants: 20
  • From 12 Dec 2021 to the primary completion date, 30 Dec 2023
  • 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

  • Patients who were considered unfit for operative treatment or refuse surgery.

Other illness

  • Distal rectal cancers(equal or less than 10cm from the anal verge)
  • Patients with signs of peritonitis and/or bowel perforation
  • Patients with unresectable colorectal cancer, or planning for palliative treatment.

Other

  • Patients who did not give informed consent
  • Patients with suspected or proven metastatic adenocarcinoma;

Who the study is looking for

  • 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

Age in the registry: 18 years to 80 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Beijing Chaoyang Hospital, Capital Medical University
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BeijingChinaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.