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Efficacy and Safety of Apatinib for Recurrent or Metastatic Esophageal Squamous Cell Carcinoma

Primary Purpose

Esophageal Neoplasms

Status
Completed
Phase
Phase 2
Locations
China
Study Type
Interventional
Intervention
Apatinib
Sponsored by
Fudan University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Esophageal Neoplasms

Eligibility Criteria

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

Inclusion Criteria:

  1. Patient age: ≥18 years old
  2. An ECOG score of 0-2
  3. Pathologically diagnosed with Esophageal Squamous Cell Carcinoma.
  4. At least second-line treatment failure regimens without targeted therapy.
  5. Measurable lesion.
  6. An expected survival of ≥ 3 months.
  7. Major organ function had to meet the following criteria:

1)For regular test results: HB(hemoglobin) ≥ 90g / L (14 days without blood transfusion); ANC(absolute neutrophil count) ≥ 1.5 × 109 / L; PLT(platelet) ≥ 80 × 109 / L 2)Biochemical tests results: Bilirubin <1.5 times the upper limit of normal (ULN) ALT(Alanine aminotransferase) and AST≤2.5 × ULN; liver metastases, if any, the ALT and AST≤5 × ULN; Endogenous creatinine clearance≥50ml/min (Cockcroft-Gault formula) 8. Informing consent.

Exclusion Criteria:

  1. Previously or presently suffering from other malignancies, except for the cured and stable carcinoma;
  2. Pregnant or lactating women;
  3. Participation in clinical trials with other drugs in the preceding four weeks.
  4. Factors that could have an effect on oral medication (such as inability to swallow, chronic diarrhea and intestinal obstruction).
  5. Serious bleeding events within 4weeks (≥3 degree)-CTCAE(Common Terminology Criteria for Adverse Events) 4.0
  6. Central nervous system metastasis or a history of central nervous system metastasis.
  7. Hypertension and antihypertensive drug treatment that does not normalize blood pressures (systolic blood pressure> 140 mmHg and diastolic blood pressure > 90 mm Hg); With unstable angina pectoris; Arrhythmia; Coronary heart disease greater than Class II; Angina pectoris diagnosed with 3 months or myocardial infarction event occurs within 6 months before recruiting.
  8. With the open wounds or fractura.
  9. A history of organ transplant.
  10. Coagulation dysfunction (PT(prothrombin time)>16 s, APTT(activated partial thromboplastin time)>43 s, TT(thrombin time)>21 s, Fbg(Fibrinogen)<2g/L), a tendency to bleed or receiving thrombolytic or anticoagulant therapy.
  11. A history of abuse of psychotropic drugs or mental disorders.
  12. Central nervous system disorders.
  13. A history of immunodeficiency.
  14. Arterial/venous thrombosis events within 12 months before recruiting.
  15. Use of CFDA(China Food and Drug Administration) approved anti-gastric modern traditional Chinese medicine preparations and immunomodulatory agents.

Sites / Locations

  • Shanghai Yangpu District East Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Apatinib Treatment

Arm Description

Apatinib for Recurrent or Metastatic Esophageal Squamous Cell Carcinoma

Outcomes

Primary Outcome Measures

Progression Free Survival
the time with no progression from the treatment

Secondary Outcome Measures

Overall Survival
the time from the treatment to death
Overall Response Rate
partial response and complete response

Full Information

First Posted
August 20, 2017
Last Updated
January 24, 2021
Sponsor
Fudan University
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1. Study Identification

Unique Protocol Identification Number
NCT03274011
Brief Title
Efficacy and Safety of Apatinib for Recurrent or Metastatic Esophageal Squamous Cell Carcinoma
Official Title
Efficacy and Safety of Apatinib for Recurrent or Metastatic Esophageal Squamous Cell Carcinoma: A Phase II, Prospective, Single-arm, Multicenter Trial
Study Type
Interventional

2. Study Status

Record Verification Date
February 2019
Overall Recruitment Status
Completed
Study Start Date
July 1, 2017 (Actual)
Primary Completion Date
March 15, 2019 (Actual)
Study Completion Date
June 26, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Fudan 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
There is no standard treatment strategy for recurrent or metastatic esophageal squamous cell carcinoma patients now, especially after the second-line treatment. Most of the patients have the bad ECOG (Eastern Cooperative Oncology Group) score and prognosis. Chemotherapy, radiotherapy, surgery are usually unacceptable for them. Previous data showed that apatinib treatment significantly improved OS(overall survival) and PFS(progression-free survival) with an acceptable safety profile in patients with advanced gastric cancer refractory to two or more lines of prior chemotherapy. The study will observe the efficacy and safety of Apatinib for recurrent or metastatic esophageal squamous cell carcinoma: A phase II, prospective, single-arm, multicenter trial.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Esophageal Neoplasms

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
40 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Apatinib Treatment
Arm Type
Experimental
Arm Description
Apatinib for Recurrent or Metastatic Esophageal Squamous Cell Carcinoma
Intervention Type
Drug
Intervention Name(s)
Apatinib
Intervention Description
Apatinib is a small-molecule tyrosine kinase inhibitor (TKI) that highly selectively binds to and strongly inhibits vascular en-dothelial growth factor receptor 2 (VEGFR-2), with a decrease in VEGF-mediated endothelial cell migration, proliferation, and tumor microvascular density. Previous data showed that apatinib treatment significantly improved OS and PFS with an acceptable safety profile in patients with advanced gastric cancer refractory to two or more lines of prior chemotherapy. Our study will observe the efficacy and safety of Apatinib for recurrent or metastatic esophageal squamous cell carcinoma: A phase II, prospective, single-arm, multicenter trial.
Primary Outcome Measure Information:
Title
Progression Free Survival
Description
the time with no progression from the treatment
Time Frame
12 weeks
Secondary Outcome Measure Information:
Title
Overall Survival
Description
the time from the treatment to death
Time Frame
24 weeks
Title
Overall Response Rate
Description
partial response and complete response
Time Frame
4 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patient age: ≥18 years old An ECOG score of 0-2 Pathologically diagnosed with Esophageal Squamous Cell Carcinoma. At least second-line treatment failure regimens without targeted therapy. Measurable lesion. An expected survival of ≥ 3 months. Major organ function had to meet the following criteria: 1)For regular test results: HB(hemoglobin) ≥ 90g / L (14 days without blood transfusion); ANC(absolute neutrophil count) ≥ 1.5 × 109 / L; PLT(platelet) ≥ 80 × 109 / L 2)Biochemical tests results: Bilirubin <1.5 times the upper limit of normal (ULN) ALT(Alanine aminotransferase) and AST≤2.5 × ULN; liver metastases, if any, the ALT and AST≤5 × ULN; Endogenous creatinine clearance≥50ml/min (Cockcroft-Gault formula) 8. Informing consent. Exclusion Criteria: Previously or presently suffering from other malignancies, except for the cured and stable carcinoma; Pregnant or lactating women; Participation in clinical trials with other drugs in the preceding four weeks. Factors that could have an effect on oral medication (such as inability to swallow, chronic diarrhea and intestinal obstruction). Serious bleeding events within 4weeks (≥3 degree)-CTCAE(Common Terminology Criteria for Adverse Events) 4.0 Central nervous system metastasis or a history of central nervous system metastasis. Hypertension and antihypertensive drug treatment that does not normalize blood pressures (systolic blood pressure> 140 mmHg and diastolic blood pressure > 90 mm Hg); With unstable angina pectoris; Arrhythmia; Coronary heart disease greater than Class II; Angina pectoris diagnosed with 3 months or myocardial infarction event occurs within 6 months before recruiting. With the open wounds or fractura. A history of organ transplant. Coagulation dysfunction (PT(prothrombin time)>16 s, APTT(activated partial thromboplastin time)>43 s, TT(thrombin time)>21 s, Fbg(Fibrinogen)<2g/L), a tendency to bleed or receiving thrombolytic or anticoagulant therapy. A history of abuse of psychotropic drugs or mental disorders. Central nervous system disorders. A history of immunodeficiency. Arterial/venous thrombosis events within 12 months before recruiting. Use of CFDA(China Food and Drug Administration) approved anti-gastric modern traditional Chinese medicine preparations and immunomodulatory agents.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
kuaile zhao, doctor
Organizational Affiliation
Radiation Oncology Department, Fudan University Cancer Center, Shanghai, P.R. China.
Official's Role
Principal Investigator
Facility Information:
Facility Name
Shanghai Yangpu District East Hospital
City
Shanghai
State/Province
Shanghai
ZIP/Postal Code
200433
Country
China

12. IPD Sharing Statement

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Efficacy and Safety of Apatinib for Recurrent or Metastatic Esophageal Squamous Cell Carcinoma

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