| Eligibility |
Inclusion Criteria:
1. Age: 18-75 years (inclusive) (Whichever is on the day of signing the informed consent
form).
2. Gastric adenocarcinoma or adenocarcinoma of gastroesophageal junction confirmed by
histology or cytology.
3. Locally advanced or metastatic gastric adenocarcinoma or adenocarcinoma of
gastroesophageal junction that has progressed after receiving first-line systematic
treatment (defined as platinum/fluorouracil containing dual drug chemotherapy, with or
without immunotherapy).
4. Evidence of disease progression on imaging during or after the last systemic treatment
as confirmed by investigator.
5. At least one assessable lesion according to RECIST V1.1; the area should not have
received previous radiotherapy, or there should be evidence of definite progress of
the lesion after completion of radiotherapy.
6. Previous history with positive Her-2 expression requires anti-Her-2 medication;
unknown Her-2 expression should define Her-2 status before enrollment.
7. Adequate main organ function.
8. Eastern Cooperative Oncology Group (ECOG) score 0-1.
9. Expected lifetime= 3 months.
10. Female patients of childbearing age must have a negative serum pregnancy test within 7
days prior to randomization; patients must agree to take adequate contraception from
signing of ICF through 6 months after last dose, during which time women are not
breastfeeding; male patients must agree to contraception and refuse sperm donation.
11. Fully understand this clinical trial and willing to sign a written informed consent
form.
Exclusion Criteria:
1. Diagnosed as Krukenberg tumor, unless radical resection has been performed and there
is no visible tumor residue.
2. Medical history of other malignant tumors or other active malignant tumors within 5
years prior to randomization (cured local tumors, such as skin basal cell carcinoma,
skin squamous cell carcinoma, superficial bladder cancer, prostate carcinoma in situ,
cervical carcinoma in situ, breast carcinoma in situ, etc. can be included).
3. Uncontrolled serous cavity effusion requiring frequent drainage or medical
intervention within 14 days before randomization (Additional intervention is required
within 2 weeks after intervention, such as pleural effusion, abdominal effusion,
pericardial effusion, etc., excluding exfoliative cytology testing of exudate).
4. Patients with central nervous system metastasis.
5. Patients who have used paclitaxel/docetaxel in the past (except patients with disease
progression more than one year after neoadjuvant/adjuvant treatment with
paclitaxel/docetaxel).
6. Patients whose previous medical history shows dMMR/MSI-H (deficient Mismatch Repair or
High Microsatellite Instability) and who have not received immunotherapy in the past
are not suitable for enrollment, and those whose dMMR/MSI status is unknown need to
clarify the status before enrollment.
7. History of serious cardiovascular or cerebrovascular disease, including but not
limited to:
1) Serious cardiac rhythm or conduction abnormalities, such as ventricular arrhythmias
requiring clinical intervention, third degree atrioventricular block, etc; 2) Acute
coronary syndrome, congestive heart failure, stroke, or other level 3 or higher
cardiovascular events occurring within 6 months before randomization; 3) The New York Heart
Association (NYHA) heart function rating of = Grade ? or left ventricular ejection fraction
(LVEF) of<50%; 4) Long QTc syndrome or QTc interval>480 milliseconds, as well as the use of
any known concomitant medication that can prolong the QT interval; 5) Poor control of
hypertension (systolic blood pressure = 160 mmHg and/or diastolic blood pressure = 100 mmHg
during the screening period).
8. History of gastrointestinal perforation and/or fistula within 6 months before
randomization.
9. Patients with active hepatitis B(Hepatitis B surface antigen (HBsAg) or HBcAb positive,
and in the active phase of hepatitis B (HBV-DNA = 10^4 cps/mL or = 2000 IU/mL)), hepatitis
C(Hepatitis C antibody (Anti HCV) positive and tested positive for HCV RNA by PCR) or HIV.
10. Patients with severe chronic or active infections that require systemic antimicrobial,
antifungal, or antiviral therapy within 14 days before randomization. Note: Patients with
viral hepatitis are allowed to receive antiviral treatment.
11. Tuberculosis treatment history within 2 years before randomization. 12. Patients with
gastrointestinal obstruction and active inflammatory bowel disease within 28 days before
randomization.
13. Toxic reaction caused by any previous treatment has not recovered to level 1 or below
(CTCAE5.0) (excluding anemia, alopecia, fatigue, poor appetite, or other toxicities that
the investigator deems to have no safety risk to patients).
14. Received major organ surgery or invasive intervention treatment within 28 days before
randomization. Or planned to undergo systematic or local tumor resection surgery during the
study period.
15. Received intravenous chemotherapy or biopolymer therapy within 28 days before
randomization. Or received oral chemotherapy, immunotherapy (such as interleukin,
interferon, thymosin, etc.), hormone therapy, small molecule targeted therapy, or any
experimental intervention within 14 days or 5 half-lives (whichever is shorter) before the
first treatment. Received traditional Chinese medicine or traditional Chinese patent
medicines with anti-tumor indications within 14 days before randomization.
16. Have received powerful CYP3A4 inhibitor or inducer within 14 days before randomization.
17. Allergic to and/or contraindication to albumin or docetaxel. 18. Known allergy and/or
contraindication to glucocorticoids (including but not limited to active gastrointestinal
ulcers, severe hypertension, severe hypokalemia, glaucoma, etc).
19. Patients with psychiatric neurological disorders that may affect trial adherence, or
patients with a history of drug dependence/alcohol dependence.
20. Patients participated in another clinical study at the same time, unless it is an
observational (non-intervention) clinical study or is in the follow-up period of an
intervention study.
21. Other situations that the investigator thinks are not suitable for patients in this
study.
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