Camrelizumab Combined With Albumin-bound Paclitaxel and S-1 in the Treatment of Advanced Gastric Cancer

  • STATUS
    Recruiting
  • End date
    Dec 31, 2023
  • participants needed
    46
  • sponsor
    Henan Cancer Hospital
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Updated on 29 April 2022
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Summary

The purpose of this study is to investigate the safety and efficacy of Camrelizumab combined with paclitaxel (albumin binding type) and S-1 for first-line treatment of advanced gastric cancer, and to further explore the curative effect of PD - L1 expression in tumor tissue, EBV virus content, microsatellite instability (MSI), DNA mismatch repair (MMR), tumor mutation load (TMB), lymphocyte subgroup and cytokines.

Description

Gastric cancer is a common malignant tumor of digestive tract.The incidence of gastric cancer in China accounts for about half of the world's total, the incidence rate ranks second, and the mortality rate ranks second.Moreover, the proportion of early gastric cancer in China is very low, only about 20%. Most of them are in advanced stage at the time of discovery. The overall 5-year survival rate is less than 15%, which seriously threatens the health and life of Chinese people.For nearly 90% of HER2 negative patients with advanced gastric and gastroesophageal junction adenocarcinoma (g / GEJ), the current first-line treatment option is chemotherapy, and the efficacy of available drugs is very limited.The ORR of the first-line chemotherapy is about 40%, and the OS is about 10 months. New therapeutic drugs are urgently needed to improve the efficacy of advanced G/GEJ.The purpose of this study was to investigate the safety and efficacy of Camrelizumab combined with paclitaxel (albumin binding type) and S-1 for first-line treatment of advanced gastric cancer.

Details
Condition Advanced Gastric Adenocarcinoma
Treatment Camrelizumab, Albumin-bound paclitaxel, S-1
Clinical Study IdentifierNCT04675866
SponsorHenan Cancer Hospital
Last Modified on29 April 2022

Eligibility

 Yes No Not Sure

Inclusion Criteria

Age 18-75 years old, no gender limit
ECOG 0-1; estimated survival time ≥12 weeks
Histopathologically confirmed unresectable locally advanced or metastatic HER-2 negative gastric adenocarcinoma
At least one measurable lesion (RECIST1.1 standard)
Have not received systemic treatment for inoperable or metastatic gastric adenocarcinoma, past (new) adjuvant chemotherapy and adjuvant radiotherapy treatment ended to enrollment> 6 months
For local lesions (non-target lesions) palliative treatment (mainly local radiotherapy) end time to random entry time> 2 weeks
The main organs and bone marrow function are basically normal
Routine blood: neutrophils ≥1.5×109/L, platelets ≥100×109/L, hemoglobin ≥80g/L
Liver function: TBiL≤1.5×ULN; ALT/AST≤2.5×ULN (for patients with liver metastases, ≤5ULN)
Renal function: serum creatinine≤1.5×ULN and creatinine clearance rate>60mL/min
INR≤1.5×ULN and activated partial thromboplastin time ≤1.5×ULN
Voluntary participation in the clinical study; fully understands and is informed of
the study and has signed the Informed Consent Form (ICF); willing to comply
with and able to complete all trial procedures
Female subjects of childbearing age or male subjects whose sexual partners are females of childbearing age shall take effective contraceptive measures throughout the treatment period and 6 months after the treatment period

Exclusion Criteria

Patients with symptomatic central nervous system disease or meningeal metastasis; for patients with brain metastases who have received previous treatment, if the clinical condition is stable and imaging evidence does not show disease progression within 4 weeks before the first treatment, they can be considered for inclusion
Patients who have previously been treated with albumin-bound paclitaxel or paclitaxel
Received major surgery (craniotomy, thoracotomy or laparotomy), open biopsy or major traumatic injury within 28 days before enrollment, or expected major surgery during the study treatment period
Suffered from other malignant tumors in the past 5 years (except for cured skin basal cell or squamous cell carcinoma, or carcinoma in situ such as cervix and breast)
The investigator believes that it will affect the subjects' ability to receive the treatment of the study protocol and are not controlled for serious medical diseases, such as combined serious medical diseases, including severe heart disease, cerebrovascular disease, uncontrolled diabetes, uncontrolled high blood pressure, Active peptic ulcer, severe infection, etc
Symptomatic congestive heart failure or cardiac color Doppler ultrasound examination shows LVEF (left ventricular ejection fraction <50%)
Any arterial thromboembolic events, including unstable angina pectoris and cerebrovascular accidents, occurred within 6 months before being selected for treatment
A history of deep vein thrombosis, pulmonary embolism or any other serious thromboembolism within 3 months before enrollment
Participate in other clinical trials 28 days before enrollment, unless participating in observational (non-interventional) clinical research or in the follow-up phase of interventional research
Patients with a history of interstitial lung disease, non-infectious pneumonia, or active tuberculosis
Patients with congenital or acquired immune deficiency, active hepatitis B or C
The patient is using immunosuppressive agents or systemic hormone therapy to achieve immunosuppressive purposes. Those who are still using it within 2 weeks before enrollment
Patients with difficult-to-control effusion, accompanied by severe pleural effusion, abdominal effusion and other clinical symptoms
Patients with grade ≥ 2 sensory or motor neuropathy; patients with peripheral neuropathy NCT-CTCAE ≥ 2
People with a history of psychotropic drug abuse and unable to quit or patients with mental disorders
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