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Clinical Trials/NCT06688786
NCT06688786
Active, not recruiting
Not Applicable

A Pospective, Single-arm, Multicenter Clinical Trial Evaluating Preoperative Neoadjuvant mFOLFOX6 Chemotherapy in Combination With PD1 Monoclonal Antibody in MSS/pMMR Locally Advanced Rectal Cancer (FIRM Study)

Xinhua Hospital, Shanghai Jiao Tong University School of Medicine1 site in 1 country30 target enrollmentNovember 1, 2024

Overview

Phase
Not Applicable
Intervention
neoadjuvant mFOLFOX6 chemotherapy combined with PD-1 inhibitor therapy
Conditions
Locally Advanced Rectal Cancer (LARC)
Sponsor
Xinhua Hospital, Shanghai Jiao Tong University School of Medicine
Enrollment
30
Locations
1
Primary Endpoint
Pathological complete response
Status
Active, not recruiting
Last Updated
3 months ago

Overview

Brief Summary

Preoperative neoadjuvant chemoradiotherapy can induce tumor regression and reduce the risk of postoperative recurrence, serving as the standard treatment for locally advanced rectal cancer. However, neoadjuvant radiotherapy may increase the risk of postoperative complications, proctitis, enteritis, and reduced anal function. Exploring radiation-free approaches to prevent the effects of radiotherapy toxicity on postoperative complications and quality of life is now a significant research focus. Neoadjuvant chemotherapy represents a promising approach in the neoadjuvant treatment of rectal cancer. Neoadjuvant chemotherapy avoids the impact of radiotherapy on organ function, reduces the incidence of postoperative anastomotic leakage, and is beneficial for long-term anal function preservation. However, its low tumor regression rate limits its application in the neoadjuvant treatment of rectal cancer. For patients with locally advanced rectal cancer, there is an urgent need for a new neoadjuvant treatment strategy that can both significantly improve tumor regression rates and reduce the risk of postoperative anastomotic leakage, and protect long-term anal function. PD-1 inhibitors are highly effective in treating microsatellite instability-high (MSI-H) colorectal cancer patients, but show poor efficacy in the 95% of patients with microsatellite stable (MSS) tumors. The challenge now is to find combination therapies that can convert tumors into an "immune-activated tumor," thereby enhancing the effectiveness of immunotherapy in MSS patients. Oxaliplatin and 5-fluorouracil have roles in releasing tumor antigen epitopes, activating CD8+ cells, and reshaping the immune microenvironment. Multiple clinical studies and animal experiments have shown that combining PD-1 antibodies with FOLFOX generates a synergistic effect, showing strong antitumor activity. This study evaluates the efficacy, safety, and impact on postoperative anal function of preoperative neoadjuvant treatment with FOLFOX chemotherapy combined with PD-1 inhibitors in patients with MSS-type advanced rectal cancer. The radiotherapy-free approach aims to avoid radiotherapy-related toxicity, offering significant potential to enhance the efficacy of neoadjuvant chemotherapy, improve long-term survival, and protect anal function.

Registry
clinicaltrials.gov
Start Date
November 1, 2024
End Date
December 31, 2027
Last Updated
3 months ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Tingyu Wu

Principal Investigator

Xinhua Hospital, Shanghai Jiao Tong University School of Medicine

Eligibility Criteria

Inclusion Criteria

  • Advanced (cT3-4NxM0 or cTxN+M0) rectal cancer with the lower tumor margin within 15 cm of the anal verge
  • Histopathology confirmed adenocarcinoma with an pMMR/MSS genetic profile.
  • Absence of bowel obstruction, or bowel obstruction relieved by proximal colostomy.
  • No prior chemotherapy, radiotherapy, targeted therapy, or immunotherapy received.
  • Female participants must be non-lactating, with a negative pregnancy test result.

Exclusion Criteria

  • Patients with distant metastasis
  • History of receiving chemotherapy, radiotherapy, targeted therapy, or immunotherapy.
  • Active autoimmune disease requiring systemic treatment within the 2 years prior to enrollment.
  • History of other malignancies within the past 5 years, excluding cured cervical carcinoma in situ or basal cell carcinoma of the skin.
  • History of HIV infection, or active chronic hepatitis B or C with high viral DNA copy numbers.
  • Patients with active tuberculosis currently receiving anti-tuberculosis treatment or treated with anti-tuberculosis therapy within the past year prior to screening.
  • Known or suspected allergy to the study drug or any study-related medications administered.
  • Presence of severe cardiovascular or cerebrovascular disease.
  • Within 14 days prior to the first dose, presence of a severe active or uncontrolled infection requiring systemic therapy, or unexplained fever \>38.5°C.
  • Receiving systemic corticosteroid treatment or other immunosuppressive agents within 14 days prior to the first dose, or immunostimulants within 4 weeks.

Arms & Interventions

Combinational treatment group

neoadjuvant mFOLFOX6 chemotherapy combined with PD-1 inhibitor therapy

Intervention: neoadjuvant mFOLFOX6 chemotherapy combined with PD-1 inhibitor therapy

Outcomes

Primary Outcomes

Pathological complete response

Time Frame: Day 7 after surgery

Major Pathological Response

Time Frame: Day 7 after surgery

Secondary Outcomes

  • Tumor regression grade(Day 7 after surgery)
  • Radiologic Response(Preoperative evaluation)
  • Postoperative complication(Within 2 weeks post-surgery)
  • Disease free survival(Three years after surgery)
  • Relapse free survival(Three years after surgery)
  • Wexner fecal incontinence scale(evaluated every 3 months for 3 years after surgery)
  • overall survival(Three years after surgery)
  • Adverse events(Prior to surgery, adverse events are evaluated the day before each chemotherapy cycle. After surgery, adverse events are evaluated at months 3, 6, 9, and 12.)
  • Neoadjuvant rectal score(Day 7 after surgery)

Study Sites (1)

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