| Eligibility |
Inclusion Criteria:
- Age=18years;
- The ECOG PS score was=1;
- Ras wild-type colorectal cancer diagnosed by histology and/or cytology has metastasis
or recurrence that cannot be cured by surgery;
- Have received at least second-line systemic anti-tumor treatments for mCRC and failed,
in which chemotherapy drugs can include fluorouracil, oxaliplatin or irinotecan; with
or without targeted drugs, such as cetuximab or bevacizumab;
- At least one measurable lesion defined according to RECIST version 1.1;
- Patients with fertility must be willing to take efficient contraceptive measures
during the study period and = 120 days after the last administration of drugs; female
patients have negative urine or serum pregnancy test results = 7 days before the first
administration of the study drugs;
- Fully understand and voluntarily sign the informed consent form;
- Organ function is good = 7 days before randomization, as shown in the following:
a.Blood transfusion or growth factor support within 2 weeks before enrollment are not
allowed to meet the enrollment criteria: i. Absolute neutrophil count (ANC) = 1.5 ×
10^9 / L; ii.Platelet count= 75 × 10^9 / L; iii.Hemoglobin=9g/dL or 90g / L or
5.6mmol/l; b. Serum total bilirubin =1.5 times the upper limit of normal value(ULN);
c. Aspartate aminotransferase (AST) and alanine aminotransferase(ALT) =2.5 times ULN,
or ALT and/or AST =5 times ULN in patients with liver metastasis; d. Serum creatinine
= 1.5 times the upper limit of normal value(ULN); e. Partial prothrombin time (APTT)
or prothrombin time (PT) =1.5 times ULN; f. Albumin =30g / L;
Exclusion Criteria:
- Any previous histological or hematological ctDNA test showed mismatch repair gene
deletion (dMMR), microsatellite instability (MSI-H), BRAF mutant patients;
- Previous immunotherapy, including anti-PD-1, anti-PD-L1, anti-CTLA-4 or any cellular
immunotherapy;
- There is active leptomeningeal disease or brain metastasis that is not well
controlled;
- History of active autoimmune diseases or autoimmune diseases that may recur. Note:
Patients with the following diseases are not excluded and can be further screened:
1. Well controlled type I diabetes mellitus
2. Hypothyroidism (controlled by hormone replacement therapy only)
3. Well controlled celiac disease
4. Skin diseases that do not require systematic treatment (e.g. vitiligo, psoriasis,
hair loss)
5. Any other disease that is not expected to recur without external triggers
- Any active malignant tumor = 5 years before the first administration of the study
drug, except the specific cancer studied in this trial and any locally recurrent
cancer that has received radical treatment (such as excised basal cell or squamous
cell skin cancer, cervical or breast cancer in situ);
- Any case requiring systemic treatment with corticosteroids (prednisone or equivalent >
10 mg / day) or other immunosuppressive drugs = 14 days before the first
administration of the study drug. Note: patients who have currently or previously used
any of the following steroid regimens are not excluded:
1. Adrenal replacement steroids (prednisone or equivalent = 10 mg / day)
2. Inhaled corticosteroids with very low local, eye, intra-articular, intranasal or
systemic absorption
3. Short term (= 7 days) prophylactic use of corticosteroids (e.g. for the treatment
of contrast medium allergy) or for the treatment of non autoimmune diseases (e.g.
delayed type hypersensitivity caused by contact allergens)
- There was uncontrolled diabetes, or over 3 grade hypoalbuminemia or >1 grade
potassium, sodium or calcium abnormalities within 14 days before the first drug
administration,
- History of interstitial lung disease, non infectious pneumonia or uncontrolled
diseases, including pulmonary fibrosis, acute lung disease, etc;
- Urine routine examination showed that urinary protein was = + +, and 24-hour urinary
protein was > 1.0 g;
- Severe chronic or active infections (including tuberculosis infection) requiring
systemic antibacterial, antifungal or antiviral treatment within 14 days before the
first administration of the study drug note: Patients with viral hepatitis are allowed
to receive antiviral treatment;
- Active mental system diseases (schizophrenia, severe depressive disorder, bipolar
disorder, etc.). Depression being treated with antidepressants is not an exclusion
criterion;
- Known history of human immunodeficiency virus (HIV) infection;
- Untreated chronic hepatitis B or chronic hepatitis B virus (HBV) carriers (HBV DNA >
500 IU / ml) or active HCV carriers with detectable HCV RNA. Note: carriers of
inactive hepatitis B surface antigen (HBsAg) and patients with stable hepatitis B (HBV
DNA < 500 IU / ml) can be included in the group;
- Any major surgery requiring general anesthesia = 28 days before the first
administration of the study drug;
- Previous heterologous stem cell transplantation or organ transplantation;
- Any of the following cardiovascular criteria
1. Cardiogenic chest pain = 28 days before the first administration of the study
drug was defined as moderate pain limiting the movement of daily living
instruments
2. Symptomatic pulmonary embolism = 28 days before the first administration of the
study drug
3. There was any history of acute myocardial infarction = 6 months before the first
administration of the study drug
4. There was any history of heart failure with NYHA grade III or IV (6) = 6 months
before the first administration of the study drug
5. There were any ventricular arrhythmia events with severity = 2 = 6 months before
the first administration of the study drug
6. There was any history of cerebrovascular accident = 6 months before the first
administration of the study drug
7. Left ventricular ejection fraction (LVEF) = lower normal limit (LLN) assessed by
multi gated acquisition (MUGA) scan or echocardiography (echo). Follow up
assessments must be performed in the same way as the baseline assessment
8. Any syncope or seizure occurring = 28 days before the first administration of the
study drug
- Hypertension with poor control after multiple drug treatment (defined as systolic
blood pressure > 140 mmHg and / or diastolic blood pressure > 90 mmHg);
- Hypersensitivity to any component of the study drug or control drug or to any
component of the container;
- Bleeding, thrombotic disease or use of anticoagulants (such as warfarin) or similar
drugs requiring therapeutic INR monitoring within 6 months before the first
administration of the study drug;
- Chemotherapy, targeted therapy, immunotherapy (e.g. interleukin, interferon, thymosin,
etc.), hormone therapy or any study therapy were performed within 14 days of the first
administration of the study drug or within 5 half lives, whichever is shorter;
- Any Chinese herbal medicine or proprietary Chinese medicine with anticancer activity
approved by China National Drug Administration within 14 days before the first
administration of the study drug (regardless of cancer type);
- Toxicity from previous anticancer treatments did not improve to baseline or stable,
except for AEs that were not considered as safety risks (e.g., hair loss, neuropathy
and specific laboratory abnormalities);
- Live vaccine was administered = 28 days before the first administration of the study
drug.
- Potential disease conditions (including laboratory abnormalities), alcohol or drug
abuse or dependence, which are not conducive to the administration of the study drug
or affect the interpretation of the toxicity and AE of the study drug, or lead to
insufficient or reduced compliance with the study;
- Participate in another clinical study at the same time, unless it is an observational
(non intervention) clinical study or is in the follow-up period of intervention study;
- Inability to swallow capsules or diseases that significantly affect gastrointestinal
function, such as malabsorption syndrome, total gastrectomy or small bowel resection,
weight loss surgery, inflammatory bowel disease or incomplete or complete intestinal
obstruction;
- Uncontrollable pleural effusion, pericardial effusion or peritoneal effusion requiring
frequent drainage or medical intervention within 7 days of the first administration of
the study drug (clinically significant recurrence, additional intervention is required
within 2 weeks after the intervention, excluding exfoliative cytology of the exudate);
- Pregnant or lactating women.
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