| Eligibility |
Inclusion Criteria:
1. The patient volunteered to participate in the study and signed an informed consent
form;
2. =18 years old; male or female
3. confirmed incurable gastric and gastroesophageal junction adenocarcinoma(unresectable
or metastatic) by pathological examination,at least have a measurable lesion without
local treatment.(According to the RECIST V1.1,the long diameter of the lesion can be
measured by spiral CT =10mm or the short diameter of the enlarged lymph nodes=15mm;
4. Adequate standard treatment was used in the past; At least two cycles of anti-PD-1 /
PD-L1 / CTLA-4 antibody therapy and platinum based chemotherapy were used in the past;
Imaging confirmed disease progression occurred during or within 12 weeks after the
treatment with anti-PD-1 / PD-L1 / CTLA-4 antibody;
5. It can provide the detection report of human epidermal growth factor receptor 2
(HER2); HER2 negative patients could be included in the study; HER2 positive patients
who had failed to receive trastuzumab treatment in the past could be included in the
study (HER2 positive was defined as = 10% of tumor cells HER2 IHC 3 + or fish
positive);
6. Swallowing pills normally;
7. ECOG score: 0~1 points;
8. Expected survival period = 12 weeks; A histological specimen can be provided for
secondary testing;
9. The main organ function meets the following criteria( It is not allowed to use any
blood components or cell growth factor drugs within 14 days before the first
medication):
The absolute value of neutrophils (ANC) = 1.5 × 109 / L; Platelet (PLT) > 100 × 109 /
L ;Albumin(ALB)= 90g / L;Total bilirubin (TBIL) = 1.5 times the upper limit of normal
(ULN); Alanine aminotransferase (ALT) Aspartate aminotransferase (AST) =3 * ULN; serum
creatinine (Cr) = 1.5 * ULN ; Thyroid stimulating hormone (TSH) = 1 × ULN (if
abnormal, FT3 and FT4 levels should be examined at the same time; if FT3 and FT4
levels are normal, they can be included in the group);Alkaline phosphatase(AKP)= 2.5
times the upper limit of normal (ULN).
10. Women of childbearing age should agree to use contraceptives (such as intrauterine
devices, contraceptives or condoms) during the study period and within 3 months after
the end of the study; negative serum or urine pregnancy test within 72 hours prior to
study enrollment and must be non-lactating patients; men should agree to patients who
must use contraception during the study period and within 3 months after the end of
the study period.
Exclusion Criteria:
1. Any active autoimmune disease or history of autoimmune disease (such as but not
limited to: autoimmune hepatitis, interstitial pneumonia, uveitis, enteritis,
hypophysitis, vasculitis, nephritis, hyperthyroidism; Patients with vitiligo or asthma
in childhood had complete remission and did not need any intervention in adulthood
were included; Asthma requiring medical intervention with bronchodilators could not be
included;
2. Those who are using immunosuppressant or systemic hormone therapy to achieve the
purpose of immunosuppression (dose > 10mg / day prednisone or other therapeutic
hormones) and continue to use them within 2 weeks before entering the group;
3. Severe allergic reaction to other monoclonal antibodies;
4. Patients who end treatment due to related toxicity during anti-PD-1 / PD-L1 / CTLA-4
antibody treatment;
5. Patients with known central nervous system metastasis (except patients with stable
disease control and asymptomatic after four weeks of radiotherapy or surgery) or
evidence of cancerous meningitis;
6. Squamous or undifferentiated carcinoma of the stomach or gastroesophageal junction;
7. The patients with ascites or pleural effusion with clinical symptoms who need puncture
drainage or who have received pleural or ascites drainage within 2 weeks before
randomization, except those who only showed a small amount of ascites or pleural
effusion without clinical symptoms;
8. Other malignant tumors in the past 3 years or at the same time (except for cured basal
cell carcinoma of skin and carcinoma in situ of cervix);
9. Patients with hypertension and cannot be well controlled after antihypertensive drug
treatment (systolic pressure = 140 mmHg or diastolic pressure = 90 mmHg);
10. There are clinical symptoms or diseases that can not be well controlled, such as: (1)
heart failure of NYHA grade 2 or above (2) unstable angina pectoris (3) myocardial
infarction within one year (4) clinically significant supraventricular or ventricular
arrhythmias need treatment or intervention (5) QTc > 450ms (male); QTc > 470ms
(female);
11. Low dose aspirin and low molecular weight heparin are allowed for prophylactic use in
patients undergoing thrombolytic or anticoagulant therapy;
12. In the first 3 months of randomization, there were significant clinical bleeding
symptoms or clear bleeding tendency, such as gastrointestinal bleeding, esophageal and
gastric varices with bleeding risk, hemorrhagic gastric ulcer or vasculitis; If the
fecal occult blood is still positive at baseline (except for weak positive and no
clinical significance judged by the researcher), gastroscopy should be performed (the
researcher can judge whether gastroscopy should be performed for those who have
undergone total gastrectomy before). If the gastroscopy results indicate severe
gastric ulcer or the risk of bleeding judged by the researcher, they can not be
enrolled; Gastrointestinal perforation or fistula occurred within 3 months before
randomization;
13. The events of arteriovenous thrombosis occurred within 6 months before entering the
group, such as cerebrovascular accidents (including transient ischemic attack,
cerebral hemorrhage, cerebral infarction), deep vein thrombosis and pulmonary
embolism, etc;
14. Known hereditary or acquired bleeding and thrombotic tendency (such as hemophilia,
coagulation dysfunction, etc.)
15. Urine routine examination showed that urine protein was = +, and 24-hour urine
protein> 1.0 g;
16. Those who had received radiotherapy, chemotherapy, surgery (except diagnostic surgery)
or trastuzumab for less than 4 weeks before randomization (palliative radiotherapy or
local treatment can be extended to 2 weeks before randomization); Or the adverse
reactions caused by previous treatment (except hair loss) did not return to = CTCAE
5.0 1level ;
17. Patients with bone metastases received palliative radiotherapy in more than 5% bone
marrow area within 2 weeks before the study;
18. Active infection, fever of unknown origin = 38.5 ? within 7 days before medication, or
white blood cell count > 15 at baseline × 109/L;
19. Congenital or acquired immune deficiency (such as HIV infection);
20. Active hepatitis (hepatitis B reference: HBsAg positive and HBV DNA > 500 IU/ml); HCV
reference: HCV antibody positive and HCV copy number > upper limit of normal value);
21. Previous treatment with camrelizumab or apatinib;
22. Live vaccine may be vaccinated less than 4 weeks before or during the study;
23. According to the judgment of the researchers, the patients may have other factors that
may affect the research results or lead to the termination of the study, such as
alcoholism, drug abuse, other serious diseases (including mental illness) requiring
combined treatment, serious laboratory abnormalities, family or social factors, which
will affect the safety of the patients.
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