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NCT Number: NCT05202314

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

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.

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Key information

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Beijing Chaoyang Hospital, Capital Medical University

Beijing, Beijing Municipality, 100020, China

Location status: Recruiting

Location contact

Zhen Jun Wang

PRINCIPAL_INVESTIGATOR

Zhen Jun Wang, M.D.

CONTACT

[email protected]

86-013601393711

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Immunotherapy (Camrelizumab)

Drug

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

Other names: Chemotheray (CAPOX or mFOLFOX6)

Primary outcomes

  1. Pathological complete remission

    Time frame: 2 weeks after patients received radical operation

    No tumor cell found in surgical specimens

Secondary outcomes

  1. Disease Free Survival

    Time frame: 3 years after operation

    No tumor regrowth or recurrence or metastasis found

  2. Overall Survival

    Time frame: 3 years after operation

    Survive during following

Study contacts

Contact information is provided by the study sponsor or research team.

Jia Gang Han, MD

CONTACT

[email protected]

+861085231604

Zhi Wei Zhai, MD

CONTACT

[email protected]

+861085231328

Sponsors and collaborators

Lead sponsor

Beijing Chao Yang Hospital

Other

Registry information

Official study title

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

Acronym: NACSOC-02

Important dates

Study start
2021
Primary completion
2023
Study completion
2026
First posted
Jan 21, 2022
Registry last updated
Feb 21, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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