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Clinical Trials/NCT05225844
NCT05225844
Unknown
Phase 2

Camrelizumab Plus Apatinib Mesylate for Advanced Gastrointestinal Cancer With Previous Standard Treatment Failure :an Exploratory, Single-arm, Open-label, Phase II Trial

Harbin Medical University1 site in 1 country150 target enrollmentJanuary 1, 2019

Overview

Phase
Phase 2
Intervention
Camrelizumab
Conditions
Gastrointestinal Cancer
Sponsor
Harbin Medical University
Enrollment
150
Locations
1
Primary Endpoint
Objective response rate (ORR)
Last Updated
4 years ago

Overview

Brief Summary

At present, surgery, radiotherapy and chemotherapy are the main treatment methods for patients with advanced gastrointestinal cancer. Although targeted therapy has significantly improved the prognosis of patients, the mortality of patients has not been significantly reduced, so new treatment methods are urgently needed. In recent years, immunotherapy has become a new hotspot in tumor therapy. Compared with traditional treatment, immune checkpoint inhibitors (ICIS) have shown long-term good efficacy and tolerance in clinical trials. However, single drug ICIS has reached a bottleneck for advanced gastrointestinal cancer, with low response rate and poor PFS and OS. With the results of REGONIVO showing good efficacy, the treatment mode of immune combined with small molecule anti angiogenesis drugs has sprung up. The purpose of this study was to analyze the efficacy and safety of in Camrelizumab combination with Apatinib mesylate in advanced gastrointestinal cancer.

Registry
clinicaltrials.gov
Start Date
January 1, 2019
End Date
October 1, 2022
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Harbin Medical University
Responsible Party
Principal Investigator
Principal Investigator

Yu Han

Chief physician

Harbin Medical University

Eligibility Criteria

Inclusion Criteria

  • Diagnosed as gastric or colorectal adenocarcinoma by histopathology and/or cytology.
  • Patients could not receive surgical resection.
  • Previous standard treatment failure .
  • According to the RECIST v1.1 guide, at least 1 lesions (never received radiotherapy),accurately measured by computed tomography (CT) or magnetic resonance imaging (MRI) (intravenous contrast agent as the first choice),the longest diameter was more than 10mm (except for the lymph nodes, the short axis of the lymph nodes must be more than 15mm), repeated measurement.
  • 5.Eastern Cooperative Oncology Group Performance Status(ECOG PS):0-1 score 6.The main organs function is normal, which meets the following requirements. (1) Blood routine examination,(no blood transfusion within 14 days).
  • Hemoglobin(HB)≥90g/L;
  • Absolute neutrophil count (ANC) ≥1.5×10\^9/L;
  • Blood platelet (PLT)≥80×10\^9/L; (2) Biochemical examination should comply with the following criteria:
  • Bilirubin(BIL) \<1.5 times of the upper limit of normal value (ULN)
  • Alanine aminotransferase (ALT) and aspartate aminotransferase(AST)\<2.5\*ULN (liver metastasis ALT and AST\<5\*ULN).

Exclusion Criteria

  • There is a case of heart disease in any of the following situations. (1)Recent publications have the following heart disease (within 6 months)
  • Acute coronary artery syndrome
  • Acute heart failure (grade III or IV of NYHA classification)
  • Significant ventricular arrhythmia(sustained ventricular tachycardia, ventricular fibrillation and sudden death after resuscitation).
  • (2)The New York Heart Association(NYHA) grade of grade III or IV (3)The patients with severe conduction block, and permanent pacemaker is invalid (two degree and three degree atrioventricular block, sinus arrest) (4)Unexplained syncope occurred within 3 months.
  • (5)The researchers identified as uncontrol of severe hypertension, or symptomatic hypertension.
  • There are many factors that affect the absorption of oral drugs (such as unable to swallow, nausea and vomiting, chronic diarrhea and intestinal obstruction).
  • ECOG score≥2
  • Abnormal coagulation function (INR\>1.5\*ULN, Activated Partial Thromboplastin Time (APTT)\>1.5\*ULN), with bleeding tendency.
  • There is any history of allergy or hypersensitivity in this research's drug or adjuvant.

Arms & Interventions

Camrelizumab Plus Apatinib mesylate

for advanced gastric cancer with previous standard treatment failure

Intervention: Camrelizumab

Camrelizumab Plus Apatinib mesylate

for advanced gastric cancer with previous standard treatment failure

Intervention: Apatinib Mesylate

Camrelizumab and Apatinib mesylate

for advanced colorectal cancer with previous standard treatment failure

Intervention: Camrelizumab

Camrelizumab and Apatinib mesylate

for advanced colorectal cancer with previous standard treatment failure

Intervention: Apatinib Mesylate

Outcomes

Primary Outcomes

Objective response rate (ORR)

Time Frame: 24 months

The proportion of patients whose tumor is reduced to a certain amount and maintain a certain period of time.

progression-free survival(PFS)

Time Frame: 24 months

the first dose until firstly confirmed and recorded disease progression or death (whichever occurs earlier)

Secondary Outcomes

  • Adverse Events(24 months)
  • Disease control rate(DCR)(24 months)
  • Overall Survival(OS)(24 months)

Study Sites (1)

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