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The Efficacy and Safety of Caffeic Acid for Esophageal Cancer (CAEC)

Primary Purpose

Esophagus Cancer

Status
Unknown status
Phase
Phase 3
Locations
China
Study Type
Interventional
Intervention
CA
placebo group
Sponsored by
The First Affiliated Hospital of Henan University of Science and Technology
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Esophagus Cancer focused on measuring esophageal cancer, caffeic acid

Eligibility Criteria

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

Inclusion Criteria:

  • Chinese
  • esophageal squamous cell cancer
  • stage IV or disease recurrence
  • chemotherapy, or radiotherapy, or palliative care is going on

Exclusion Criteria:

  • PS (performance status): ≥ 3
  • severe hepatic and renal dysfunction
  • hypercoagulability
  • thrombocytosis

Sites / Locations

  • The Clinical Medical College, The First Affiliated Hospital of Henan University of Science and Technology

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

CA group

placebo group

Arm Description

caffeic acid (300mg, tid, po) continue given until progression of disease or death, or patients are unable to bear the side effects

the same shape placebo tablets continue given until progression of disease or death, or patients are unable to bear the side effects

Outcomes

Primary Outcome Measures

overall survival (OS)
The percentage of 1 year overall survival (OS) after random allocation. The follow-up will be done every 3 months through phone call, investigator visiting, and medical recording review.

Secondary Outcome Measures

progression-free survival (PFS)
The percentage of 3 months progression-free survival (PFS) after random allocation. PFS was defined as the time from randomisation to disease progression or death as assessed by the treating physicians in the study through CT scan, gastroscopy and biopsy pathology, X-ray barium meal.

Full Information

First Posted
February 28, 2017
Last Updated
November 24, 2020
Sponsor
The First Affiliated Hospital of Henan University of Science and Technology
Collaborators
Anyang Tumor Hospital, 150th Hospital of PLA
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1. Study Identification

Unique Protocol Identification Number
NCT03070262
Brief Title
The Efficacy and Safety of Caffeic Acid for Esophageal Cancer
Acronym
CAEC
Official Title
Caffeic Acid for Advanced Esophageal Squamous Cell Cancer: A Randomized, Double-blind, and Multicenter Trial in Chinese Patients
Study Type
Interventional

2. Study Status

Record Verification Date
April 2020
Overall Recruitment Status
Unknown status
Study Start Date
January 2017 (undefined)
Primary Completion Date
December 2020 (Anticipated)
Study Completion Date
December 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
The First Affiliated Hospital of Henan University of Science and Technology
Collaborators
Anyang Tumor Hospital, 150th Hospital of PLA

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Caffeic acid can target inhibit GASC1 (gene amplified in squamous cell carcinoma 1, also known as KDM4C and JMJD2C) expression and GASC1 is confirmed to be a new oncogene in several cancers including esophageal cancer. This study aims to investigate the efficiency and safety of coffeic acid in chinese advanced esophageal squamous cell cancer (ESCC).
Detailed Description
Background: More than half of global esophageal cancer cases came from China.80 percentage patients were diagnosed with advanced disease and suffered from the poor outcome.With the development of target therapy among cancers,the overall survival and life quality of patients has been continuous improved recently.However,there had little reports focusing on target therapy in esophageal cancer . Caffeic acid as an ordinary drug is used for thrombocytopenia when patient received chemotherapy. Newly studies shown caffeic acid can target inhibit GASC1 expression, and GASC1 is confirmed to be a new oncogene in esophageal cancer. Aim: to investigate the efficiency and safety of caffeic acid in chinese advanced esophageal squamous cell cancer. Methods: 240 advanced ESCC patients will be randomized to two arms: Arm A (receiving coffeic acid treatment) or Arm B (placebo group). In Arm A, patients will receive coffeic acid treatment: 300mg, tid, po, continue to progress disease (PD) or die or the intolerant adverse events; in Arm B, the same shape placebo tablets will be deliveried to patients. 1 years follow-up for both groups patients.Patients in both arms can receive any other ways of anti cancer therapy in the same time. Primary endpoints: OS Second endpoints: PFS

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Esophagus Cancer
Keywords
esophageal cancer, caffeic acid

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
300 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
CA group
Arm Type
Experimental
Arm Description
caffeic acid (300mg, tid, po) continue given until progression of disease or death, or patients are unable to bear the side effects
Arm Title
placebo group
Arm Type
Placebo Comparator
Arm Description
the same shape placebo tablets continue given until progression of disease or death, or patients are unable to bear the side effects
Intervention Type
Drug
Intervention Name(s)
CA
Intervention Description
caffeic acid, 300mg, tid, po
Intervention Type
Drug
Intervention Name(s)
placebo group
Intervention Description
placebo tablet, 3 tablets, tid, po
Primary Outcome Measure Information:
Title
overall survival (OS)
Description
The percentage of 1 year overall survival (OS) after random allocation. The follow-up will be done every 3 months through phone call, investigator visiting, and medical recording review.
Time Frame
1 year
Secondary Outcome Measure Information:
Title
progression-free survival (PFS)
Description
The percentage of 3 months progression-free survival (PFS) after random allocation. PFS was defined as the time from randomisation to disease progression or death as assessed by the treating physicians in the study through CT scan, gastroscopy and biopsy pathology, X-ray barium meal.
Time Frame
1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Chinese esophageal squamous cell cancer stage IV or disease recurrence chemotherapy, or radiotherapy, or palliative care is going on Exclusion Criteria: PS (performance status): ≥ 3 severe hepatic and renal dysfunction hypercoagulability thrombocytosis
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Shegan Gao, PhD
Organizational Affiliation
The Clinical Medical College, The First Affiliated Hospital of Henan Science and Technology
Official's Role
Study Chair
Facility Information:
Facility Name
The Clinical Medical College, The First Affiliated Hospital of Henan University of Science and Technology
City
Luoyang
State/Province
Henan
ZIP/Postal Code
471003
Country
China

12. IPD Sharing Statement

Plan to Share IPD
Undecided
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The Efficacy and Safety of Caffeic Acid for Esophageal Cancer

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