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Camrelizumab Combined With Apatinib Mesylate Tablets, Nab-paclitaxel and S-1 in the Treatment of Locally Advanced Gastric Cancer

Primary Purpose

Advanced Gastric Cancer

Status
Active
Phase
Phase 2
Locations
China
Study Type
Interventional
Intervention
Camrelizumab
Apatinib Mesylate
nab-paclitaxel
S1
Sponsored by
Fujian Medical University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Advanced Gastric Cancer

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age: 18-70 years of age
  • Gastric adenocarcinoma was confirmed by pathology( including histology or cytology)。
  • CT/MRI,PET-CT or laparoscopic exploration were used to confirm the diagnosis of gastric cancer staging as cT2-4a and/or N+ and M0 before operation.
  • measurable lesions at least should be detected by CT/MRI examination in accordance with the RECIST1.1.(CT scan of tumor lesion length≥10mm,CT scan short diameter≥15mm,scan slice thicknes 5mm)
  • ECOG(Eastern Cooperative Oncology Group)PS(Performance Status):0-1 scores;
  • the expected survival time is more than 12 weeks
  • the main organ function is normal, which should meet the following criteria:

    (1) blood routine examination standards should be met(no blood transfusion within 14 days)

    a.HB≥ 100g/L b. WBC≥3×109/L c. ANC≥1.5×109/L d. PLT≥100×109/L (2)biochemical examination shall comply with the following criteria:

    1. BIL<1.5 normal upper limit ULN
    2. ALT and AST<2.5 ULN,GPT≤1.5×ULN
    3. Cr≤1 ULN,CCR(creatinine clearance rate)>60ml/min(Cockcroft-Gault formula)
  • women of childbearing age must have a pregnancy test in 7 days before entering the group (in serum), and the results were negative, and willing to use appropriate contraception during the study period and the last 8 weeks after giving drug test; men should have the surgical sterilization, or adopt the appropriate contraceptive methods during the test and the last 8 weeks after giving drug test。
  • No other clinical studies were conducted before and during the treatment
  • participants is willing to participate in this study, sign the informed consent, have good compliance, cooperate with follow-up.

Exclusion Criteria:

  • Previous history of chemotherapy, radiotherapy, targeted drug therapy or immunotherapy
  • Patients with contraindications for surgical treatment and chemotherapy or whose physical condition and organ function do not allow for larger abdominal surgery
  • patients with metastasis
  • Having any active autoimmune diseases or a history of autoimmune diseases (such as interstitial pneumonia, uveitis, enteritis, hepatitis, pituitary inflammation, vasculitis, myocarditis, nephritis, hyperthyroidism, hypothyroidism, including but not limited to these diseases or syndromes); Patients with vitiligo or cured childhood asthma/allergies who did not need any intervention in adulthood were excluded; Autoimmune hypothyroidism treated with a stable dose of thyroid replacement hormone; Type 1 diabetes with stable doses of insulin
  • A history of immunodeficiency, including HIV testing positive, or other acquired or congenital immunodeficiency disorders, or a history of organ transplantation and allogeneic bone marrow transplantation
  • Accompanied by serious heart, lung, liver, kidney disease; Have nerve, mental disease; Jaundice or obstruction of the digestive tract with severe infection
  • pregnant or lactating women
  • The blood pressure of patients with hypertension cannot be reduced to the normal range by the antihypertensive drugs (systolic pressure >140 mmHg, diastolic pressure >90 mmHg)
  • With Ⅰ magnitude of coronary heart disease, arrhythmia (including QTc protracted between male > 450 ms, women > 470 ms) and cardiac insufficiency
  • Patients have a clear tendency with gastrointestinal bleeding, including the following situation: local active ulcerative lesions, and fecal occult blood (+ +); with melena and hematemesis history in 2 months; and patients with fecal occult blood (+) and unresected gastric primary tumor; patients with the risk of bleeding should take the gastroscopy test, if it is the gastric cancer, and researchers believe that may results in massive digestive tract hemorrhage;coagulation dysfunction (INR(international normalized ratio)>1.5, APTT(activated partial thromboplastin time)>1.5 ULN), with bleeding tendency;
  • Subjects have failed to control good cardiovascular clinical symptoms or disease, including but not limited to: such as: (1) the NYHA class II heart failure (2) above unstable angina pectoris (3) occurred within 1 year (4) have clinical significance of myocardial infarction (mi) room sex or ventricular arrhythmias without clinical intervention on or after clinical intervention is still poorly controlled
  • History of interstitial lung disease (except radiation pneumonia without hormone therapy), and history of non-infectious pneumonia
  • Patients are positive of urine protein (urine protein detection 2+ or above, or 24 hours urine protein quantitative >1.0g);
  • A person who has previously been allergic to any component of camrilizumab or to any component of the drug under study
  • The researchers consider those who were not suitable for inclusion.

Sites / Locations

  • Fujian Medical University Union Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Camrelizumab + Apatinib + nab-paclitaxel +S-1

nab-paclitaxel +S-1

Arm Description

Camrelizumab combined with Apatinib mesylate tablets, nab-paclitaxel and S-1 in the treatment of locally advanced gastric cancer

nab-paclitaxel and S-1 in the treatment of locally advanced gastric cancer

Outcomes

Primary Outcome Measures

major pathological response
major pathological response(MPR)

Secondary Outcome Measures

pathological complete response
pathological complete response (pCR)
Objective response rate
Objective response rate (ORR) according to Response Evaluation Criteria in Solid Tumours (RECIST) version. 1.1, and immune-related (ir) RECIST
R0 resection rate
The surgical procedure was total or subtotal gastrectomy with 3 weeks after total neoadjuvant therapy.

Full Information

First Posted
December 10, 2019
Last Updated
September 3, 2023
Sponsor
Fujian Medical University
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1. Study Identification

Unique Protocol Identification Number
NCT04195828
Brief Title
Camrelizumab Combined With Apatinib Mesylate Tablets, Nab-paclitaxel and S-1 in the Treatment of Locally Advanced Gastric Cancer
Official Title
Camrelizumab Combined With Apatinib Mesylate Tablets, Nab-paclitaxel and S-1 in the Treatment of Locally Advanced Gastric Cancer: an Multicenter, Open, Randomized, Controlled Clinical Study
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
June 18, 2020 (Actual)
Primary Completion Date
July 22, 2022 (Actual)
Study Completion Date
March 31, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Fujian Medical University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
To evaluate the clinical efficacy and safety of camrelizumab combined with apatinib mesylate, nab-paclitaxel and S-1

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Advanced Gastric Cancer

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
53 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Camrelizumab + Apatinib + nab-paclitaxel +S-1
Arm Type
Experimental
Arm Description
Camrelizumab combined with Apatinib mesylate tablets, nab-paclitaxel and S-1 in the treatment of locally advanced gastric cancer
Arm Title
nab-paclitaxel +S-1
Arm Type
Active Comparator
Arm Description
nab-paclitaxel and S-1 in the treatment of locally advanced gastric cancer
Intervention Type
Drug
Intervention Name(s)
Camrelizumab
Intervention Description
Camrelizumab One course will last 21 days.Given once every 3 weeks at a dose of 200 mg.
Intervention Type
Drug
Intervention Name(s)
Apatinib Mesylate
Intervention Description
Apatinib One course will last 21 days.Oral administration at a dose of 250 mg everyday。
Intervention Type
Drug
Intervention Name(s)
nab-paclitaxel
Intervention Description
nab-paclitaxel One course will last 21 days。Given twice every 3 weeks at a dose of 125 mg/m2.
Intervention Type
Drug
Intervention Name(s)
S1
Intervention Description
S-1 was calculated according to body surface area , P.O., bid, d1-d14。And the dosage according body surface area:<1.25m2, 40mg every time;1.25-1.5m2,50mg every time; >1.5m2, 60mg every time
Primary Outcome Measure Information:
Title
major pathological response
Description
major pathological response(MPR)
Time Frame
4 months
Secondary Outcome Measure Information:
Title
pathological complete response
Description
pathological complete response (pCR)
Time Frame
4 months
Title
Objective response rate
Description
Objective response rate (ORR) according to Response Evaluation Criteria in Solid Tumours (RECIST) version. 1.1, and immune-related (ir) RECIST
Time Frame
4 months
Title
R0 resection rate
Description
The surgical procedure was total or subtotal gastrectomy with 3 weeks after total neoadjuvant therapy.
Time Frame
4 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age: 18-75 years of age Gastric adenocarcinoma was confirmed by pathology( including histology or cytology)。 CT/MRI,PET-CT or laparoscopic exploration were used to confirm the diagnosis of gastric cancer staging as cT2-4a and/or N+ and M0 before operation. measurable lesions at least should be detected by CT/MRI examination in accordance with the RECIST1.1.(CT scan of tumor lesion length≥10mm,CT scan short diameter≥15mm,scan slice thicknes 5mm) ECOG(Eastern Cooperative Oncology Group)PS(Performance Status):0-1 scores; the expected survival time is more than 12 weeks the main organ function is normal, which should meet the following criteria: (1) blood routine examination standards should be met(no blood transfusion within 14 days) a.HB≥ 100g/L b. WBC≥3×109/L c. ANC≥1.5×109/L d. PLT≥100×109/L (2)biochemical examination shall comply with the following criteria: BIL<1.5 normal upper limit ULN ALT and AST<2.5 ULN,GPT≤1.5×ULN Cr≤1 ULN,CCR(creatinine clearance rate)>60ml/min(Cockcroft-Gault formula) women of childbearing age must have a pregnancy test in 7 days before entering the group (in serum), and the results were negative, and willing to use appropriate contraception during the study period and the last 8 weeks after giving drug test; men should have the surgical sterilization, or adopt the appropriate contraceptive methods during the test and the last 8 weeks after giving drug test。 No other clinical studies were conducted before and during the treatment participants is willing to participate in this study, sign the informed consent, have good compliance, cooperate with follow-up. Exclusion Criteria: Previous history of chemotherapy, radiotherapy, targeted drug therapy or immunotherapy Patients with contraindications for surgical treatment and chemotherapy or whose physical condition and organ function do not allow for larger abdominal surgery patients with metastasis Having any active autoimmune diseases or a history of autoimmune diseases (such as interstitial pneumonia, uveitis, enteritis, hepatitis, pituitary inflammation, vasculitis, myocarditis, nephritis, hyperthyroidism, hypothyroidism, including but not limited to these diseases or syndromes); Patients with vitiligo or cured childhood asthma/allergies who did not need any intervention in adulthood were excluded; Autoimmune hypothyroidism treated with a stable dose of thyroid replacement hormone; Type 1 diabetes with stable doses of insulin A history of immunodeficiency, including HIV testing positive, or other acquired or congenital immunodeficiency disorders, or a history of organ transplantation and allogeneic bone marrow transplantation Accompanied by serious heart, lung, liver, kidney disease; Have nerve, mental disease; Jaundice or obstruction of the digestive tract with severe infection pregnant or lactating women The blood pressure of patients with hypertension cannot be reduced to the normal range by the antihypertensive drugs (systolic pressure >140 mmHg, diastolic pressure >90 mmHg) With Ⅰ magnitude of coronary heart disease, arrhythmia (including QTc protracted between male > 450 ms, women > 470 ms) and cardiac insufficiency Patients have a clear tendency with gastrointestinal bleeding, including the following situation: local active ulcerative lesions, and fecal occult blood (+ +); with melena and hematemesis history in 2 months; and patients with fecal occult blood (+) and unresected gastric primary tumor; patients with the risk of bleeding should take the gastroscopy test, if it is the gastric cancer, and researchers believe that may results in massive digestive tract hemorrhage;coagulation dysfunction (INR(international normalized ratio)>1.5, APTT(activated partial thromboplastin time)>1.5 ULN), with bleeding tendency; Subjects have failed to control good cardiovascular clinical symptoms or disease, including but not limited to: such as: (1) the NYHA class II heart failure (2) above unstable angina pectoris (3) occurred within 1 year (4) have clinical significance of myocardial infarction (mi) room sex or ventricular arrhythmias without clinical intervention on or after clinical intervention is still poorly controlled History of interstitial lung disease (except radiation pneumonia without hormone therapy), and history of non-infectious pneumonia Patients are positive of urine protein (urine protein detection 2+ or above, or 24 hours urine protein quantitative >1.0g); A person who has previously been allergic to any component of camrilizumab or to any component of the drug under study The researchers consider those who were not suitable for inclusion.
Facility Information:
Facility Name
Fujian Medical University Union Hospital
City
Fuzhou
State/Province
Fujian
ZIP/Postal Code
350000
Country
China

12. IPD Sharing Statement

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Camrelizumab Combined With Apatinib Mesylate Tablets, Nab-paclitaxel and S-1 in the Treatment of Locally Advanced Gastric Cancer

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