| Eligibility |
Inclusion Criteria:
1. Aged between 18 and 75 years;
2. Has histologically or cytologically diagnosed with unresectable locally advanced or
metastatic gastric adenocarcinoma (GC) including gastroesophageal junction
adenocarcinoma;
3. Human epidermal growth factor receptor 2 (HER2) negative: immunohistochemical (IHC) -
or +; IHC ++ and fluorescence in situ hybridization (FISH) -;
4. No previous systemic therapy (chemotherapy, targeted therapy, immunotherapy,
biological therapy, etc.) for GC/GEJ. Subjects with previous adjuvant/neo-adjuvant
therapy completed more than 6 months can be enrolled. Anti-tumor traditional Chinese
medicine is forbidden within 2 weeks before the first cycle chemotherapy. Patients are
allowed to receive palliative radiotherapy (primary tumor or metastasis), but lesions
in radiation field cannot be defined as target lesions for assessing objective
response, and radiotherapy-related adverse reactions must be restored to at least
grade 1;
5. Expected survival time = 3 months;
6. Eastern Cooperative Group (ECOG) performance status score 0 or 1;
7. Weight =40kg, or BMI>18;
8. 1 measurable lesions at least should be detected by CT/MRI examination in accordance
with the RECIST(Response Evaluation Criteria In Solid Tumors)1.1;
9. All acute toxic events (excluding hair loss, fatigue and hearing loss) caused by
previous anti-tumor treatments or surgery are alleviated to grade 0-1 (according to
NCI CTCAE version 5.0) or to the level specified by the inclusion/exclusion criteria
of this study;
10. The main organ function of cases should be normal, and meet the following criteria:
? Absolute neutrophil count (ANC)=1.5×109/L, platelet (PLT) =80×109/L;
? Total bilirubin (TBIL) <1.5 upper limit of normal (ULN), ALT (glutamic-pyruvic
transaminase)and AST(glutamic-oxalacetic transaminase)=2.5ULN. For subjects with liver
metastases, ALT and AST=5 ULN, serum Cr=1.5ULN or endogenous creatinine clearance
>50ml /min (Cockcroft-Gault formula);
? International normalized ratio (INR) <1.5, prothrombin time (PT) and activated
partial thromboplastin time (APTT) = 1.5 ULN;
? Urine protein<2+; if urine protein=2+, the 24-hour urine protein quantitative
detection value must be =1g;
11. Females of childbearing potential (FOCBP), who are not surgically sterile or
postmenopausal, must conduct pregnancy test (serum or urine) within 7 days before
enrollment, and the results are negative, and willing to use appropriate contraception
during the study period until at least 3 months after the last administration of the
test drugs. Non-sterilized males who are sexually active must agree to use adequate
contraception during the study period a until at least 3 months after the last
administration of the test drugs;
12. Fully understand the study and voluntarily sign the informed consent form (ICF);
willing and able to comply with planned visits, treatments, laboratory examinations
and other procedures.
Exclusion Criteria:
1. HER2 positive cancer: IHC+++, IHC++ and FISH+;
2. Pathological classification of tumor is squamous carcinoma or undifferentiated
carcinoma or other types;
3. The interval between disease progression and previous anti-tumor therapy for locally
advanced is less than six months;
4. Central nervous system(CNS)metastases with clinical symptoms for example cerebral
edema, spinal cord compression, cancerous meningitis, leptomeningeal disease, and/or
progressive growth. For subjects with CNS metastases that have been adequately
treated, and the neurological symptoms can return to baseline levels at least 2 weeks
before enrollment (except for residual signs or symptoms related to treatment), can be
enrolled. In addition, subjects must stop corticosteroids at least 2 weeks before
enrollment;
5. Gastrointestinal bleeding that could not be effectively controlled; gastrointestinal
perforation and/or gastrointestinal fistula occurred within 6 months before
enrollment; arterial/venous thrombosis occurred within 6 months before enrollment,
such as cerebrovascular accidents (including temporary ischemic attacks, cerebral
hemorrhage, cerebral infarction), deep vein thrombosis and pulmonary embolism;
6. Pleural fluid, ascites, or pericardial effusion that could not be controlled within 7
days before enrollment;
7. Weight loss is more than 20% within 2 months before enrollment;
8. Major surgery performed within 28 days before enrollment (tissue biopsy for diagnosis
and central venous catheter placement via peripheral vein are allowed). used
immunosuppressive drugs within 7 days before enrollment, excluding nasal spray and
inhaled corticosteroids or physiological doses of systemic steroid hormones (=10 mg/d
prednisone or equivalent other kinds of corticosteroids);
9. Other malignancy disease history within five years, with the exception of basal cell
carcinoma or squamous carcinoma of skin, superficial bladder carcinoma, and carcinoma
in situ (such as Intraductal carcinoma in situ of the breast, cervical cancer in situ,
etc.);
10. With history of check point inhibitor treatment, for instance PD-1/PD-L1/
PD-L2/CD137/CTLA-4 antibody agent, and other drug stimulatory or co-inhibitory T-cell
receptor;
11. Any active or suspected autoimmune diseases. Subjects who do not require systemic
immunosuppressive therapy can be enrolled, such as type I diabetes, hypothyroidism
that only requires hormone replacement therapy, and skin diseases that do not require
systemic therapy (such as white scar wind, silver Scourge etc.).
12. Preexisting peripheral neuropathy >Grade 1;
13. Inability to swallow, chronic diarrhea and intestinal obstruction, or other factors
that may affect the administration and absorption of the drug;
14. Has active infectious diseases, interstitial lung diseases, non-infectious pneumonia,
or other systemic diseases that can not be controlled (such as diabetes, hypertension,
pulmonary fibrosis, etc.);
15. Has a known history of HIV infection or AIDS. Has a known history of untreated or
active hepatitis (active hepatitis B, defined as HBV-DNA>500 IU/ml; active hepatitis
C, defined as HCV-RNA higher than the upper limit of the analytical method), or
co-infection of HBV and HCV;
16. Hypertension (systolic blood pressure>140 mmHg or diastolic blood pressure>90 mmHg)
that cannot be well controlled by antihypertensive drugs.
17. The following conditions occur within 6 months before enrollment: myocardial
infarction, severe/unstable angina, NYHA grade 2 or higher cardiac insufficiency,
clinically significant supraventricular or ventricular arrhythmia, and symptomatic
congestion heart failure;
18. The use of antibiotics> 7 days within 2 weeks before enrollment, or unexplained fever>
38.5°C within 1 week before the treatment of this study (fever caused by tumors can be
enrolled);
19. Has an allogenic tissue/solid organ transplant history;
20. Participated in any other clinical trials of drug within 4 weeks before enrollment, or
less than 5 half-lives after the last study drug administrated.
21. Be allergic to the study drug or excipients; or have a severe allergic history to
other monoclonal antibodies;
22. Has a known history of drug abuse;
23. Has a history or current evidence of any condition that might increase the risk of
patients in the present trial, confound the results of the study, interfere with the
cases' participation for the full duration of the study, or be not in the best
interest of the participant to participate, in the opinion of the investigators.
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