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GASC1 Inhibitor Caffeic Acid for Squamous Esophageal Cell Cancer (ESCC) (GiCAEC)

Primary Purpose

Esophagus Cancer, Stage III

Status
Unknown status
Phase
Phase 3
Locations
China
Study Type
Interventional
Intervention
Caffeic acid
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, Stage III focused on measuring esophageal cancer, caffeic acid

Eligibility Criteria

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

Inclusion Criteria:

  1. Chinese
  2. esophageal squamous cell cancer
  3. stage IV or recurrence disease
  4. chemotherapy, or radiotherapy, or palliative care is going on

Exclusion Criteria:

  1. PS (performance status): ≥ 3
  2. severe hepatic and renal dysfunction
  3. hypercoagulability
  4. thrombocytosis

Sites / Locations

  • Anyang Tumor HospitalRecruiting
  • The Clinical Medical College, The First Affiliated Hospital of Henan University of Science and TechnologyRecruiting
  • Nanyang Central HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Arm A

Arm B

Arm Description

In Arm A: 40 patients will receive coffeic acid treatment: 100-200mg, tid, po, 2 weeks treated then 1 week black interval (weight >50kg, 200mg per time, weight < or =50kg, 100mg per time)

In Arm B: 40 patients will receive the placebo tablets: 100-200mg, tid, po, 2 weeks treated then 1 week black interval.

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
November 24, 2020
Last Updated
December 1, 2020
Sponsor
The First Affiliated Hospital of Henan University of Science and Technology
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1. Study Identification

Unique Protocol Identification Number
NCT04648917
Brief Title
GASC1 Inhibitor Caffeic Acid for Squamous Esophageal Cell Cancer (ESCC)
Acronym
GiCAEC
Official Title
GASC1 Inhibitor Caffeic Acid for Advanced Squamous Esophageal Cell Cancer (ESCC): a Multicenter, Phase II Trial (GiCAEC)
Study Type
Interventional

2. Study Status

Record Verification Date
November 2020
Overall Recruitment Status
Unknown status
Study Start Date
May 1, 2019 (Actual)
Primary Completion Date
May 1, 2021 (Anticipated)
Study Completion Date
May 1, 2022 (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

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
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: 80 advanced ESCC patients who failed to the chemotherapy or chemoradiotherapy (1 or 2 line) will be randomized to two arms: arm A and arm B. In arm A, 40 patients will receive coffeic acid treatment: 100-200mg, tid, po, 2 weeks treated then 1 week black interval(weight >50kg, 200mg per time, weight < or =50kg, 100mg per time; in arm B, 40 patients will receive the placebo tablets. 1 years follow-up for all patients in this trial. 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, Stage III
Keywords
esophageal cancer, caffeic acid

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Model Description
1:1 Randomized grouping
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
80 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Arm A
Arm Type
Experimental
Arm Description
In Arm A: 40 patients will receive coffeic acid treatment: 100-200mg, tid, po, 2 weeks treated then 1 week black interval (weight >50kg, 200mg per time, weight < or =50kg, 100mg per time)
Arm Title
Arm B
Arm Type
Placebo Comparator
Arm Description
In Arm B: 40 patients will receive the placebo tablets: 100-200mg, tid, po, 2 weeks treated then 1 week black interval.
Intervention Type
Drug
Intervention Name(s)
Caffeic acid
Intervention Description
40 patients will receive coffeic acid treatment: 100-200mg, tid, po, 2 weeks treated then 1 week black interval(weight >50kg, 200mg per time, weight < or =50kg, 100mg per time)
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 recurrence disease chemotherapy, or radiotherapy, or palliative care is going on Exclusion Criteria: PS (performance status): ≥ 3 severe hepatic and renal dysfunction hypercoagulability thrombocytosis
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Shegan Gao, Ph.D
Phone
+86 18638859977
Email
gsg112258@163.com
First Name & Middle Initial & Last Name or Official Title & Degree
Ruinuo Jia, Ph.D
Phone
+86 18537950766
Email
jiaruinuo@163.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Shegan Gao, Ph.D
Organizational Affiliation
The Clinical Medical College, The First Affiliated Hospital of Henan Science and Technology
Official's Role
Study Chair
Facility Information:
Facility Name
Anyang Tumor Hospital
City
Anyang
State/Province
Henan
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Fuyou Zhou, MD,PhD
Phone
+86 13939998799
Email
jiaruinuo@163.com
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
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Shegan Gao, PhD
Phone
0379 64811906
Email
gsg112258@163.com
First Name & Middle Initial & Last Name & Degree
Ruinuo Jia, MD
Phone
0379 64815350
Email
jiaruinuo@163.com
First Name & Middle Initial & Last Name & Degree
Tanyou Shan, MD
First Name & Middle Initial & Last Name & Degree
Guoqiang Kong, MD
First Name & Middle Initial & Last Name & Degree
Xiaozhi Yuan, MD
First Name & Middle Initial & Last Name & Degree
Ruina Yang, MD
First Name & Middle Initial & Last Name & Degree
Jing Ren, MD
First Name & Middle Initial & Last Name & Degree
Wei Wang, MD
First Name & Middle Initial & Last Name & Degree
Ruinuo Jia, MD, Ph.D
Facility Name
Nanyang Central Hospital
City
Nanyang
State/Province
Henan
ZIP/Postal Code
473000
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Lixin Wan, MD

12. IPD Sharing Statement

Citations:
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Citation
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Citation
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PubMed Identifier
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Citation
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Citation
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Citation
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Citation
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GASC1 Inhibitor Caffeic Acid for Squamous Esophageal Cell Cancer (ESCC)

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