Study of Oral Metronidazole on Postoperative Chemotherapy in Colorectal Cancer
- Conditions
- Colorectal Cancer Stage IIIColorectal Cancer Stage II
- Interventions
- Drug: Placebo oral tablet
- Registration Number
- NCT04264676
- Lead Sponsor
- Shanghai Jiao Tong University School of Medicine
- Brief Summary
Fusobacterium nucleatum (Fusobacterium nucleatum, Fn) has been identified as an independent risk factor for recurrence of colorectal cancer. In this study, oral metronidazole would be used to reduce the abundance of Fn in patients with high Fn, so as to explore whether oral metronidazole can improve the efficacy of postoperative chemotherapy in patients with colorectal cancer.
- Detailed Description
Gut microbiota are linked to chronic inflammation and carcinogenesis. Chemotherapy failure is the major cause of recurrence and poor prognosis in colorectal cancer patients. Previously in the investigators' research, the investigators find the contribution of gut microbiota to chemoresistance in patients with colorectal cancer. The investigators found that Fusobacterium nucleatum (Fn) was abundant in colorectal cancer tissues in patients with recurrence post chemotherapy, and was associated with patient clinicopathological characterisitcs. Furthermore, the investigators' bioinformatic and functional studies demonstrated that Fn promoted colorectal cancer resistance to chemotherapy. Metronidazole has been known to treat with anaerobe infection, including Fusobacterium. So oral metronidazole would be used to reduce the abundance of Fn in patients with high Fn, so as to explore whether oral metronidazole can improve the efficacy of postoperative chemotherapy in patients with colorectal cancer.
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 294
- Individuals aged 18-75 years
- Individuals firstly confirmed by surgery pathology as colorectal cancer (AJCC cancer staging II - III), who need mFOLFOX6 or CapeOX postoperative chemotherapy
- Individuals with Fn - deltaCT value in colon tissue samples detected by qPCR ≥-12 before receiving chemotherapy
- Individuals who could tolerate chemotherapy drugs: ECOG (Eastern Cooperative Oncology Group) score ≤2 points, WBC(White Blood Cell) ≥4.0×10^9/L, Hb （Hemoglobin） ≥80g/L, PLT （Platelet） ≥80×10^9/L, ALT （Alanine Aminotransferase）< 2ULN （Upper Limmit of Normal）, Scr （Creatinine）< 1.5ULN
- Individuals who participate this study and sign the informed consent form willingly.
- Individuals with colorectal adenoma or non-colorectal cancer, such as inflammatory bowel disease
- Individuals with a history of familial adenomatous polyposis (FAP)
- Individuals with severe heart, lung, brain, kidney, gastrointestinal or systemic diseases
- Individuals who used antibiotics for more than 5 days in 1 month prior to chemotherapy
- Individuals with stage I or IV colorectal cancer, or with stage II colorectal cancer who do not need postoperative chemotherapy
- Individuals with contraindications for metronidazole
- Individuals who unwilling to participate this study，or unwilling to sign the informed consent form
- Individuals with any conditions that the researchers considered inappropriate for inclusion
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Placebo Placebo oral tablet supplement of identical-appearing placebo 0.4g three times per day for 7 days, which is one treatment every 4 weeks for mFOLFOX6 (6 treatments totally),and every 6 weeks for CapeOX 4 treatments totally). Metronidazole Metronidazole Oral Tablet supplement of metronidazole 0.4g three times per day for 7 days, which is one treatment every 4 weeks for mFOLFOX6(6 treatments totally),and every 6 weeks for CapeOX (4 treatments totally).
- Primary Outcome Measures
Name Time Method Disease Free Survival, DFS 5 years The time from the initial surgical treatment of colorectal cancer to the earliest evidence of recurrence.
- Secondary Outcome Measures
Name Time Method Overall Survival, OS 5 years The time from the initial surgical treatment of colorectal cancer to death from any cause.
Recurrence Rate, RR 3 years, 5 years Percentage of patients who has recurrence during or after chemotherapy with Metronidazole or Placebo.
Trial Locations
- Locations (4)
Division of Gastroenterology and Hepatology, Ren-Ji Hospital, Shanghai Jiao-Tong University School of Medicine, Shanghai Institute of Digestive Disease; Key Laboratory of Gastroenterology & Hepatology, Ministry of Health
🇨🇳Shanghai, Shanghai, China
Zhongshan Hospital affiliated to Fudan University
🇨🇳Shanghai, Shanghai, China
Fudan University Shanghai Cancer Center
🇨🇳Shanghai, Shanghai, China
Ruijin Hospital affiliated to Shanghai Jiao Tong University School of Medicine
🇨🇳Shanghai, Shanghai, China