| Eligibility |
Inclusion Criteria:
1. Age =18 years;
2. The ECOG PS score of the eastern United States cancer cooperation group was 0 or 1;
3. Ras wild-type colorectal cancer diagnosed by histology and / or cytology has
metastasis or recurrence that cannot be cured by surgery;
4. Have received at least second-line systemic anti-tumor treatment for MCRC and failed,
in which chemotherapy drugs can include fluorouracil, oxaliplatin and irinotecan, such
as XELOX, FOLFOX, FOLFIRI, folfoxiri and xeliri; targeted drugs can be combined or
not, such as cetuximab and bevacizumab;
5. At least one measurable lesion defined according to RECIST version 1.1;
6. Patients with fertility must be willing to take efficient contraceptive measures
during the study period and = 120 days after the last administration of tirelizumab;
female patients have negative urine or serum pregnancy test results = 7 days before
the first administration of the study drug;
7. Fully understand this study and voluntarily sign the informed consent form.
Exclusion Criteria:
1. The following laboratory indicators belong to the exclusion criteria:
1. Absolute neutrophil count (ANC) < 1.5 × 109 / L, or platelet count < 100 × 109 /
L, or hemoglobin < 9g / dL or 90g / L or 5.6mmol/l; Blood transfusion or growth
factor support within 2 weeks before enrollment are not allowed to meet the
enrollment criteria;
2. Serum total bilirubin > 1.5 times the upper limit of normal value (ULN); Patients
with liver metastasis > 2.5 times ULN;
3. Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) > 2.5 times
ULN, or ALT and / or ast > 5 times ULN in patients with liver metastasis;
4. Serum creatinine > 1.5 times the upper limit of normal value (ULN), or creatinine
clearance < 60ml / min (calculated according to Cockcroft Gault formula);
5. Partial prothrombin time (APTT) or prothrombin time (PT) > 1.5 times ULN (subject
to the normal value of clinical trial and Research Center);
6. Albumin < 30g / L;
7. Clinically significant electrolyte abnormalities;
2. Any previous histological or hematological ctDNA test showed mismatch repair gene
deletion (dmmr), microsatellite instability (MSI-H) and BRAF mutant patients;
3. Previous immunotherapy, including anti-PD-1, anti-PD-L1, anti-CTLA-4 or any cellular
immunotherapy;
4. Have a history of active autoimmune disease or autoimmune disease that may recur;
5. Patients with any disease requiring systemic treatment with corticosteroids (the dose
of prednisone or equivalent drug > 10 mg / day) or other immunosuppressive drugs
within = 14 days before the administration of the first study drug need not be
excluded if they have used any of the following steroid treatment schemes at present
or in the past:
1. Adrenal replacement steroids (dose of prednisone or equivalent = 10 mg / day);
2. Local, ocular, intra-articular, intranasal or inhaled corticosteroids with very
low 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);
6. there are a history of interstitial lung disease, non infectious pneumonia, pulmonary
fibrosis, acute lung disease, or poorly controlled systemic diseases (including but
not limited to diabetes, hypertension, etc.).
7. Clinically uncontrollable diarrhea;
8. chronic or active infections require systemic antibacterial, antifungal or antiviral
treatment, including tuberculosis infection. Patients with a history of active
tuberculosis infection = 1 year before screening should also be excluded, unless proof
can be provided that appropriate treatment has been completed;
9. Brain metastasis or leptomeningeal metastasis;
10. Clinically significant pleural effusion, pericardial effusion or ascites need to be
drained for many times within 2 weeks before the first administration of the study
drug;
11. There is a clinically detectable second primary malignant tumor at the time of
enrollment, or there have been other malignant tumors in the past 5 years (except
fully treated skin basal cell carcinoma or cervical carcinoma in situ);
12. despite the use of standard care, patients with poor control of diabetes or poor
electrolyte control are still in control.
13. Known history of human immunodeficiency virus infection;
14. Untreated patients with chronic hepatitis B or chronic hepatitis B virus (HBV)
carriers with HBV DNA higher than 500 IU / ml and patients with positive hepatitis C
virus (HCV) RNA should be excluded. Inactive hepatitis B surface antigen (HBsAg)
carriers, treated and stable hepatitis B (HBV DNA < 500 IU / ml), and cured hepatitis
C patients were all selected;
15. Any major surgical operation = 28 days before the administration of the first study
drug;
16. Previous allogeneic stem cell transplantation or organ transplantation;
17. Uncontrollable hypertension, i.e. systolic blood pressure > 140mmHg or diastolic blood
pressure > 90mmHg after single drug treatment;
18. At present, there are gastrointestinal diseases such as duodenal ulcer, ulcerative
colitis and intestinal obstruction, or other conditions that may cause
gastrointestinal bleeding or perforation determined by the researchers; Or those who
have a history of intestinal perforation and intestinal fistula and are not cured
after surgical treatment;
19. Patients with a history of arterial thrombosis or deep venous thrombosis within 6
months before enrollment, or with evidence or history of bleeding tendency within 2
months before enrollment, regardless of severity;
20. Stroke or transient ischemic attack occurred within 12 months before enrollment;
21. Skin wound, operation site, wound site, severe mucosal ulcer or fracture are not fully
healed;
22. Acute myocardial infarction, severe / unstable angina pectoris or coronary artery
bypass grafting within 6 months before enrollment; Or patients with cardiac
insufficiency of NYHA grade 2 or above;
23. Severe hypersensitivity to other monoclonal antibodies, irinotecan and its excipients;
24. Have received any systemic chemotherapy within 28 days before the first study drug, or
received immunotherapy (such as interleukin, interferon, thymosin), hormone therapy,
targeted therapy, or any research therapy within 14 days or 5 half lives before the
first study drug, whichever is shorter;
25. Received any Chinese herbal medicine or proprietary Chinese medicine for cancer
control within 14 days before the first study drug;
26. Patients whose toxic and side effects (due to previous anticancer treatment) have not
returned to baseline or stable levels, unless it is not considered that such AE may
pose safety risks (such as hair loss, neuropathy and specific laboratory
abnormalities);
27. Have received live vaccine within 4 weeks (including) before the first administration
of the study drug; Seasonal influenza vaccines are usually inactivated, so they are
allowed to be used; Intranasal vaccine belongs to live vaccine, so it is not allowed
to be used;
28. The investigator considers that the subject has any clinical or laboratory
abnormalities or compliance problems and is not suitable to participate in this
clinical study;
29. Serious psychological or mental abnormalities;
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