Apatinib Combined With Chemotherapy for Esophageal Squamous Cell Cancer After the Failure of Standard Treatment

Esophageal Squamous Cell Carcinoma Clinical Trial

Official title:

Apatinib Combined With Chemotherapy for Esophageal Squamous Cell Cancer After the Failure of Standard Treatment

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT03224221
• Other study ID #: AHAT-103
• Status: Recruiting
• Phase: Phase 2
• First received: July 19, 2017
• Last updated: July 19, 2017
• Start date: March 23, 2017
• Est. completion date: June 23, 2019

Study information

• Verified date: June 2017
• Source: The First Affiliated Hospital of Anhui Medical University
• Contact: Guoping Sun, Ph.D.
• Phone: 0551-62922249
• Email: gpsun_ahmu[@]126.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

We conduct the clinical trial to further explore the efficacy and safety of Apatinib combined with chemotherapy in treating recurrent or metastatic esophageal squamous cell carcinoma after the failure of conventional treatments.

Description:

Esophageal cancer is one of the most common malignant tumor and esophageal squamous cell carcinoma is the main pathological type of esophageal carcinoma in China. Treatment of recurrent or metastatic esophageal squamous cell carcinoma is usually poor. New treatments were needed. Apatinib, which was approved by CFDA (China Food and Drug Administration) for the treatment of advanced gastric cancer, is a small molecule tyrosine kinase inhibitor. It competes with intracellular VEGFR-2's ATP binding sites highly and selectively, thereby blocking downstream signaling to achieve the goal of inhibiting neovascularization in tumor tissue. We have observed in clinical practice that some patients with esophageal squamous cell carcinoma have benefited from the treatment of apatinib. So we conduct a phase II clinical trial to explore the efficacy and safety of Apatinib combined with chemotherapy (platinum and fluorouracil) in treating recurrent or metastatic esophageal squamous cell carcinoma after the failure of conventional treatments.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 189
• Est. completion date: June 23, 2019
• Est. primary completion date: January 23, 2019
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• 1.Male or female patients, age:=18 years old.

• 2.Confirmed by histology of recurrent or metastatic esophageal squamous cell carcinoma.

• 3.Patients who undergo local or recurrent metastases after surgery and / or radiotherapy and chemotherapy,at least one measurable lesion(tumor lesions CT scan length = 10 mm,lymph node lesions CT scan short diameter = 15 mm,scan layer thickness is not greater than 6 mm).

• 4.The ECOG physical status score: 0 to 2.

• 5.Expected survival = 3 months.

• 6.Subjects received other treatment damage have been restored, which received nitroso or mitomycin interval = 6 weeks; to accept other cytotoxic drugs, radiotherapy or surgery = 4 weeks, and the wound has been completely healed;

• 7.The main organs function properly:

1. blood routine examination standards to be met (14 days without blood transfusion and blood products):

1. HB=90g/L;

2. ANC=1.5×109/L;

3. PLT=80×109/L;

2. biochemical tests to meet the following criteria:

1. TBIL<1.5×ULN;

2. ALT and AST<2.5×ULN, and <5×ULN for patients with liver metastases

3. Serum Cr=1.5×ULN or endogenous creatinine clearance> 45ml/min (Cockcroft-Gault formula);

• 8.The women of childbearing age must have taken reliable contraceptive measures or have a pregnancy test (serum or urine) within 7 days prior to enrollment and have a negative result and are willing to use the appropriate method at 8 weeks after the trial and the last given test contraception.For the man, consent should be given to appropriate contraception or surgical sterilization 8 weeks after the trial and at the last time the test drug was given;

• 9.Patients should be voluntary to the trial and provide with signed informed consent

Exclusion Criteria:

• 1.Pregnant or lactating women;

• 2.Patients with high blood pressure and who can not be reduced to normal range by antihypertensive therapy (systolic blood pressure> 140 mmHg, diastolic blood pressure> 90 mmHg) with myocardial infarction or myocardial infarction, arrhythmia and grade II heart Incomplete function;

• 3.Have a significant impact on oral drug absorption factors, such as unable to swallow, chronic diarrhea and intestinal obstruction;

• 4.Coagulation dysfunction(INR>1.5 or prothrombin time (PT)>ULN + 4 seconds or APTT>1.5×ULN),with bleeding tendency or are receiving thrombolytic or anticoagulant therapy;

• 5.with a clear gastrointestinal bleeding concerns (such as local active ulcer lesions, fecal occult blood + + above), 6 months of history of gastrointestinal bleeding;

• 6.Central nervous system metastasis with symptoms;

• 7.The investigator judged other circumstances that will affect the conduct of the study and the outcome of the study

Related Conditions & MeSH terms

• Carcinoma, Squamous Cell
• Esophageal Neoplasms
• Esophageal Squamous Cell Carcinoma
• Neoplasms, Squamous Cell

Intervention

Drug:
• Apatinib
Patients will receive Apatinib at 500mg/times,oral one times daily for 28 days
• fluorouracil and platinum
the dosage of the fluorouracil and platinum need to be determined by the doctors according to the actual condition of the patients

Locations

Country	Name	City	State
China	First Affiliated Hospital of Anhui Medical University	Hefei	Anhui

Sponsors (1)

Lead Sponsor	Collaborator
The First Affiliated Hospital of Anhui Medical University

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	One-year survival rate	The probability of survival in one year	12 months
Secondary	Progress free survival(PFS)		From date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 100 months
Secondary	Overall survival		From date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 100 months
Secondary	Incidence of Treatment-Emergent Adverse Events	Safety evaluation according to the CTCAE4.0 standard, once every 1 cycle assessment	Each follow up visit, assessed up to 12 months
Secondary	Quality of life using EORTC QLQ C30 - scale	Life quality evaluation using EORTC QLQ C30 - scale,once every 1 cycle assessment	From date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 12 months