Overview

Colon cancer is one of the most lethal malignancies, and colorectal cancer ranks the fifth leading cause of tumor-related mortality in China. FOLFOX is the recommended adjuvant/ neoadjuvant treatment for advanced colon cancer. JS001, as the first Chinese produced anti-PD-1 monoclonal antibody, has been approved by CFDA. This study aims to assess the safety and efficacy of JS001 in combination with FOLFOX as adjuvant/neoadjuvant treatment for patients with locally advanced colon cancer.

Eligibility

Inclusion Criteria:

1. Locally advanced colon cancer patients diagnosed by pathologic biopsy，and the patients have defined indications for neoadjuvant chemotherapy by MDT group.
2. Patients may be available to undergo surgery.
3. Patient has at least 1 measurable lesions according to RECIST version 1.1;
4. Males and females aged ≥18 years.
5. ECOG score 0-1; Estimate life ≥1 year.
6. The main organs and bone marrow function are basically normal:

        (1) Blood test White blood cell count (WBC)≥2000/mm^ 3; Absolute neutrophil count
        (ANC)≥1000/mm^ 3; Blood platelet count ≥100000/mm^ 3; Hemoglobin ≥9g/d; Serum creatine ≤
        2.0mg/dL; (2) Liver function Serum total bilirubin (TBIL) is within the normal range
        (normal range specified by the institution; Total bilirubin of Gilbert syndrome <3.0mg/dL);
        Serum Aspartate Transaminase (AST), serum Alanine Aminotransferase Transaminase (ALT) and
        alkaline phosphatase (ALP) ≤ 2.5 * upper limit of normal (ULN); International normalized
        ratio (INR) ≤1.5(or the patient is taking Warfarin for a long time, INR=2-3), and
        prothrombin time (PTT) ≤ULN (3) Pulmonary function Carbon Monoxide Diffusing Capacity
        (DLCO) ≥70% predictive OR; DLCO<70% and ≥55% , and the maximal oxygen consumption VO2 max
        ≥10L/min/Kg (cardiopulmonary assessment) or 6 minute walk experiment ≥500 meters; Patients
        with DLCO <55% are not included in this study; Pulse oximetry at rest or walking ≥92% (4)
        Cardiac function Baseline ECG showes no PR interval prolongation or atrioventricular block;
        7. Patient and his/her mate must agree to follow instructions for method of contraception
        for the duration of the study period and within 6 months of the end of the study (eg.
        Intrauterine device, birth control pills or condoms); Serum or urine pregnancy test is
        negative within 7days prior to study enrollment and must be non-lactating; 8. Patients
        voluntarily joined the study, signed informed consent document, and were well compliant and
        able to be followed up with testers.
        Exclusion Criteria:
          1. Any previous active autoimmune disease (including any history of inflammatory bowel
             disease), or history of diseases to be treated with systemic steroids or
             immunosuppressive drugs(except for vitiligo patients）；
          2. Use vaccines against infectious diseases (such as flu, chickenpox, etc.) within 4
             weeks (28 days) of starting the study treatment;
          3. Active systemic infection requiring treatment, positive detection of hepatitis B
             surface antigen or hepatitis C ribonucleic acid (RNA);
          4. A known positive history or positive test result of human immunodeficiency virus or
             acquired immunodeficiency syndrome (AIDS);
          5. Patients with any severe and/or uncontrolled diseases, such as (1)unstable angina
             pectoris, symptomatic congestive heart failure, myocardial infarction within 6 months
             before randomization, severe uncontrolled arrhythmia；Patients with unsatisfactory
             blood pressure control (systolic blood pressure >140mmHg,diastolic blood
             pressure>90mmHg); (2) active or uncontrolled severe infection; (3) liver diseases such
             as cirrhosis, (4) decompensated liver disease, chronic active hepatitis; poor diabetes
             control (fasting blood glucose (FBG)> 10mmol/L); (5) urinary routine indicates urinary
             protein>or=++, and confirmed 24-hour urine protein quantitative >1.0g; (6) having a
             history of psychotropic substance abuse and being unable to quit or have mental
             disorders;
          6. Pevious treatment with any anti-tumor treatment, including but not limited to
             chemotherapy, radiotherapy, immunotherapy (such as anti-PD-1, anti-PD-L1, anti-PD-L2
             or anti-CTLA-4 antibodies or any other antibodies that target the T cell co-regulatory
             pathway), etc; Tumor-related therapies or online anticancer drugs are currently being
             used; Anticoagulant is currently in use; Received major surgery in the past 3weeks;
          7. Studies with previous malignancies, unless complete remission is achieved at least 2
             years prior to the start of the study and no other treatment (subjects with basal cell
             carcinoma of skin and carcinoma in situ of cervix will not be excluded from the
             study);
          8. History of previous interstitial lung disease, drug-induced interstitial lung disease,
             radiation pneumonitis, symptomatic interstitial lung disease, or evidence of any
             activepneumonia found on chest CT scans within 4 weeks prior to the first study drug
             treatment.
          9. Immunosuppressive drugs were used within 2weeks prior to the first study drug
             treatment, excluding topical glucocorticoids, systemic glucocorticoids ≤ 10mg/day of
             prednisone or equivalent doses of other glucocorticoids;
         10. Pregnant or lactating female;
         11. Prisoners who are illegally imprisoned or compulsory for non-mental illness or
             physical (eg infectious disease) illness;
         12. Patients with bleeding tendency (such as active gastrointestinal ulcers) or treatment
             with anticoagulants or vitamin K antagonists such as warfarin, heparin or the like;
         13. A history of allergic reactions to the interventions;
         14. According to the investigator's judgment, there are serious concomitant diseases that
             endanger the safety of the patient or affect the patient's completion of the study;
        16. Has received a vaccine within 30 days prior to the study.