| Eligibility |
Inclusion Criteria:
1. Patients voluntarily participated in the study and signed informed consent;
2. Age between 18 and 75;
3. Agreed to detect the expression status of PD-L1 biomarker;
4. ECOG score is 0 or 1, and the expected survival time is not less than 3 months;
5. Histologically confirmed recurrent or metastatic squamous cell carcinoma,
adenocarcinoma, and adenosquamous carcinoma with documented disease progression. Note
that histological confirmation of the original primary tumor is required by
pathological reports;
6. Patients with recurrent or metastatic cervical cancer who had received at least once
platinum-based systemic chemotherapy were included;
7. The patient is not suitable for local treatment (surgery or radiotherapy cannot be
performed);
8. Patients with measurable lesions as defined in RECIST1.1 criteria;
9. The main organs function is well, and the laboratory test indexes meet the following
requirements:(1) Routine blood test (no blood transfusion or hematopoietic stimulating
factor was used within 7 days before screening) :? Hemoglobin (HB) = 90g/L;? Absolute
neutrophil count (ANC) =1.5×109/L;? Platelet (PLT) = 80×109/L;(2) Blood biochemical
test (no blood transfusion or albumin within 7 days before screening) :? ALT and AST
=2.5 × ULN (liver/bone metastasis =5 × ULN;Bone metastases =5 ULN);? Serum total
bilirubin (TBIL) =1.5 × ULN;? Serum Cr=1.5×ULN or creatinine clearance =60 mL /min;(3)
Coagulation function test:? Activated partial thrombin time (APTT), international
standardized ratio (INR), prothrombin time (PT) = 1.5×ULN;? Doppler ultrasound
assessment: left ventricular ejection fraction (LVE F)= 50%;
10. Any toxic side effects of previous chemotherapy have been recovered to =CTCAE1 or
baseline level;
11. The patient has the ability to take medication orally;
12. Women of reproductive age must agree to use a highly effective method of contraception
during the study period and for 6 months after the last administration of the study
drug;Negative serum or urine pregnancy test within 7 days prior to study enrollment
and must be non-lactating subjects;
Exclusion Criteria:
1. Patients with a history or signs of brain metastases;
2. Prior use of bevacizumab, antiangiogenic drugs and other antiangiogenic drugs;
3. Received anti-tumor monoclonal antibody treatment within 4 weeks before enrollment;
Had previously received other PD-1/PD-L1 antibodies and anti-CTLA-4 (cytotoxic
T-lymphocyte associated antigen-4) therapy.
4. Patients were receiving immunosuppressant or systemic hormone therapy for
immunosuppression (dose > 10mg/ day of prednisone or other equivalent hormone) and
were still using 2 weeks prior to enrollment
5. Participate in other clinical trials or complete other clinical trials within 4 weeks;
6. Abnormal coagulation function (INR > 2.0, PT > 16s), bleeding tendency or receiving
thrombolytic or anticoagulant therapy;
7. Failed to recover from adverse events (except hair loss) after prior medication use;
8. The patient has any active autoimmune disease or a history of autoimmune disease;
9. Clinical symptoms or diseases of the heart that are not well controlled;
10. Congenital or acquired immune deficiency;
11. Received chemotherapy, targeted and radiotherapy within 2 weeks before enrollment;
12. Concomitant diseases/History:(1) Clinically significant hemoptysis occurred within 3
months before enrollment (hemoptysis > 50ml per day);Or bleeding symptoms of
significant clinical significance or a clear bleeding tendency, such as
gastrointestinal bleeding, hemorrhagic gastric ulcer, baseline fecal occultation and
above, or suffering from vasculitis, etc.;(2) Arteriovenous thrombosis events occurred
within 6 months before enrollment, such as cerebrovascular accident (including
temporary ischemic attack), deep venous thrombosis (except those who had been cured
after intravenous catheterization due to chemotherapy) and pulmonary embolism,
etc.;(3) hypertension, which cannot be well controlled by antihypertensive drug
therapy (systolic blood pressure >140 mmHg or diastolic blood pressure >90
mmHg);During the first 6 months of randomization, myocardial infarction,
severe/unstable angina, NYHA grade 2 or higher cardiac dysfunction, clinically
significant ventricular arrhythmias or ventricular arrhythmias, and symptomatic
congestive heart failure;(4) Interstitial lung disease, non-infectious pneumonia or
uncontrollable systemic diseases (e.g., diabetes, pulmonary fibrosis and acute
pneumonia);(5) Renal insufficiency: urine protein = ++ indicated by routine urine
examination, or confirmed 24-hour urine protein level =1.0g; (6) History of live
attenuated vaccine vaccination within 28 days prior to initial study administration or
expected live attenuated vaccine vaccination during study period;(7) human
immunodeficiency virus (HIV) infection or known acquired immunodeficiency syndrome
(AIDS);Active hepatitis (hepatitis B, defined as HBV-DNA = 500 IU/ mL;Hepatitis C,
defined as hcV-RNA higher than the lower limit of assay) or co-infection with
hepatitis B and c;(8) Severe infection, including but not limited to bacteremia and
severe pneumonia requiring hospitalization, occurred within 4 weeks before the first
administration;Active infection with CTCAE grade =2 requiring systemic antibiotic
treatment within 2 weeks prior to initial administration, or fever of unknown origin
>38.5°C during screening/prior to initial administration (as determined by the
investigator, fever due to tumor can be included);Evidence of active tuberculosis
infection within 1 year before administration;(9) Have been diagnosed with any other
malignant tumor within 3 years prior to entry into the study;(10) Major surgery
performed within 28 days before enrollment (tissue biopsy and peripheral venipuncture
placement of central venous catheter [PICC] required for diagnosis are permitted);
13. Subjects who have received or are planning to receive allogeneic bone marrow
transplantation or solid organ transplantation;
14. Peripheral neuropathy = grade 2;Patients with active brain metastases, cancerous
meningitis, spinal cord compression, or diseases of the brain or pia meningeal found
by imaging CT or MRI examination at the time of screening (patients with brain
metastases who had completed treatment 14 days before enrollment and had stable
symptoms could be enrolled, but were confirmed to have no symptoms of cerebral
hemorrhage by craniocerebral MRI, CT or venography evaluation);
15. There are significant factors affecting oral drug absorption, such as inability to
swallow, chronic diarrhea, and presence of clinically significant intestinal
obstruction.
16. Corrected QT interval > 470 msec;If a patient has a prolonged QT interval, but the
investigator assessed the cause of the prolonged QT interval as pacemaker (and no
other cardiac abnormalities), discussion with other study physicians will be required
to determine whether the patient is eligible for inclusion.
17. Known allergic to pharmaceutical ingredients;
18. Female subjects who are pregnant, breast-feeding, or planning to become pregnant
during the study period.
19. Patients with other serious physical or mental disorders or abnormal laboratory tests
that may increase the risk of study participation or interfere with study results, and
who are considered unsuitable for study participation by the investigator.
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