| Eligibility |
Inclusion Criteria:
- Histologically confirmed gastric adenocarcinoma, which is diagnosed as unresectable
locally advanced, recurrent or metastatic gastric and gastroesophageal junction
adenocarcinoma (including signet-ring cell carcinoma, mucinous adenocarcinoma,
hepatoid adenocarcinoma).
- Pathological results showed that the expression of HER-2 was positive (IHC score 3+,
or IHC score 2+ and ISH score positive) or low (IHC score 1+, or IHC score 2+ and ISH
score negative) in gastric adenocarcinoma.
- Failed to receive first-line system medication of gastric carcinoma chemotherapy.
- Male or female, aged 18-75 years old.
- ECOG score 0-2.
- Life expectancy more than 12 weeks.
- There is at least one measurable or assessable focus (According to RECIST 1.1).
- Patients who received radical radiotherapy within 3 months before entering the study
are eligible to participate in this study if the radiation area of bone marrow is less
than 30%.
- The function of main organs and bone marrow function are normal, defined as follows:
- Blood test:
- White blood cell (WBC) = 4.5*103 / mm3;
- Absolute neutrophil count (ANC) = 1.5*103 / mm3;
- Blood platelet count = 100*103 / mm3;
- hemoglobin = 9.0g/dL (no transfusion or erythropoietin dependence within 7 days).
- Liver function:
- Serum total bilirubin (TBIL) = 1.5 times of upper limit of normal (ULN);
- Serum Aspartate Transaminase (AST) and serum Alanine Aminotransferase For
patients without liver metastasis, Transaminase (ALT) = 2.5 times of ULN;
- For patients with liver metastasis, ALT or AST = 5 times of ULN.
- Renal function:
- Serum creatinine (Cr) = 1.5 times of ULN or Cr clearance = 60 mL/min
(Cockcroft-Gault formula);
- Urinary protein (UPRO) < 2+ or Quantification of 24-hour urinary protein < 1g.
- Coagulation function:
- International normalized ratio (INR) = 1.5 times of ULN or prothrombin time (PT)
= 1.5 times of ULN; within 7 days before treatment.
- If the subject is receiving anticoagulant therapy, PT is within the range of
anticoagulant.
- Cardiac function:
- New York Heart Association (NYHA) grade < 3;
- Left ventricular ejection fraction = 50%;
- The baseline of ECG is no atrioventricular block or PR interval prolongation.
- Pulmonary function:
- Carbon Monoxide Diffusing Capacity (DLCO) = 70% predicted OR;
- DLCO < 70% and = 55%, the maximal oxygen consumption (VO2max) = 10 L/min/kg
(cardiopulmonary assessment) or 6-minutes walk test over 500 meters;
- Patients with DLCO under 55% are excluded from this study;
- Pulse oximetry at walking or rest is over 92%.
- The patient and her/his mate should agree to contracept for the time of the study
period and within six months after the study (see Section 4.3).
- Patients join the study voluntarily, sign the informed consent file, and be able to
comply with the visit and related procedures stipulated in the program.
Exclusion criteria:
- Signs of active bleeding in the focus.
- Previously received anti-PD-1 antibody, anti-PD-L1 antibody, anti-PD-L2 antibody,
anti-CD137 antibody, anti-CTLA-4 antibody, or other antibodies or drugs targeting T
cell costimulatory or checkpoint pathways.
- Be allergic to the active ingredients or excipients of Sintilimab or disitamab
vedotin;
- Participate in another interventional clinical study (except observational clinical
study or follow-up phase of an intervention study) at the same time;
- Received systemic treatment with anti-tumor indications of proprietary Chinese
medicine or immunomodulatory drugs (eg. thymosin/interferon/interleukin, except drugs
used locally to control pleural effusion or ascites) within 2 weeks before the first
dose.
- Received immunosuppressive drugs within 4 weeks before the first dose of the study,
excluding nasal, inhaled or other topical glucocorticoids or physiological doses of
systemic glucocorticoids (i.e., no more than 10mg/d prednisone or equivalent doses of
other glucocorticoids), or the use of hormones for the prevention of contrast medium
allergy.
- Live attenuated vaccine may be received within 4 weeks before the first dose of study
treatment or during the study period.
- Note: inactivated injection virus vaccine for seasonal influenza is allowed.
- Surgical procedures were performed within 4 weeks before the first dose of study
treatment, or major surgery was expected during the study treatment;
- Laparoscopic exploratory surgery was performed within 2 weeks before the first dose of
study treatment.
- There was toxicity (excluding alopecia, non-clinically significant, and asymptomatic
laboratory abnormalities) caused by previous antineoplastic therapy that did not
return to Grade 0 or 1 in the NCICTCAEv5.0 before the first dose.
- Patients with symptomatic central nervous system cancer metastasis or cancerous
meningitis. For previously treated patients with central nervous system cancer
metastasis, if their condition is stable (there is no evidence of imaging progress at
least 4 weeks before the first administration of the trial treatment, and repeated
imaging tests confirm that there is no evidence of new brain metastasis or enlargement
of the original brain metastasis), they can participate in the trial in the case they
do not need steroid therapy within 14 days before the first dose of the trial
treatment.
- Patients with ascites could be found by physical examination; Only imaging shows a
small amount of ascites but no symptoms can be selected.
- Patients with moderate amount of bilateral pleural effusion, or large amount of
pleural effusion on one side, or patients who have caused respiratory dysfunction and
need drainage.
- Patients with bone metastasis at risk of paraplegia.
- Patients with or suspected autoimmune diseases within 2 years (patients with vitiligo,
psoriasis, alopecia or Graves' disease who do not need systematic treatment in the
past 2 years, patients with hypothyroidism who only need thyroid hormone replacement
therapy and type I diabetes patients who only need insulin replacement therapy can be
enrolled in the group).
- History of primary immunodeficiency.
- Active pulmonary tuberculosis.
- History of allogeneic organ transplantation and allogeneic hematopoietic stem cell
transplantation.
- History of human immunodeficiency virus (HIV) infection (i.e. HIV antibody positive).
- Severe infection that is active or poorly controlled clinically.
- Symptomatic congestive heart failure (NYHA grade II-IV) or poorly controlled
arrhythmia.
- Arterial hypertension (systolic blood pressure = 160mmHg or diastolic blood pressure =
100mmHg) that is still uncontrolled even with standard treatment.
- Arterial thromboembolism occurred within 6 months, including myocardial infarction,
unstable angina pectoris, cerebrovascular accident or transient ischemic attack.
- There is a history of deep venous thrombosis, pulmonary embolism or any other severe
thromboembolism within 3 months (implantable venous infusion port or catheter-derived
thrombosis, or superficial venous thrombosis is not considered "severe"
thromboembolism).
- There are uncontrolled metabolic disorders, other non-malignant organs, systemic
diseases or secondary reactions to cancer, which can lead to higher medical risk or
uncertainty in survival assessment.
- Hepatic encephalopathy, hepatorenal syndrome, Child-Pugh B grade and higher grade
liver cirrhosis.
- History of tumor-related intestinal obstruction (within 3 months before the signing of
the informed consent) or the following diseases: inflammatory bowel disease or
extensive bowel resection (partial colectomy or extensive small bowel resection,
complicated with chronic diarrhea), Crohn's disease, ulcerative colitis.
- Patients with acute or chronic active hepatitis B virus (HBsAg positive and HBVDNA
viral load = 200IU/mL or = 103copies / mL) or acute or chronic active hepatitis C
virus (HCV antibody positive and HCV RNA positive).
- Active syphilis infections who need treatment.
- There was a history of gastrointestinal perforation or fistula within 6 months before
the study, except for surgical resection of the primary focus of gastric cancer.
- Suffering from interstitial lung disease that requires steroid treatment.
- History of other primary malignant tumors, except:
- Complete remission of malignant tumors for at least 2 years before the study and no
other treatment was required during the study period
- Non-melanoma skin cancer or malignant freckle-like nevus with adequate treatment and
no evidence of disease recurrence.
- Primary cancer with adequate treatment and no evidence of disease recurrence.
- Women who are pregnant or breastfeeding.
- Other acute or chronic diseases, mental disorders or laboratory tests that may lead to
drug-related risks or interfere with the interpretation of the results of the study,
and patients are classified as ineligible to participate in this study according to
the judgment of the researchers.
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