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Prospective, random and control clinical trial of Apatinib associates with sequential chemoradiotherapy compared with simple sequential chemoradiotherapy in middle and advanced squamous cells esophageal cancer.

Prospective, random and control clinical trial of Apatinib associates with sequential chemoradiotherapy compared with simple sequential chemoradiotherapy in middle and advanced squamous cells esophageal cancer.

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IIR-17011865
Enrollment
Unknown
Registered
2017-07-04
Start date
2017-07-01
Completion date
Unknown
Last updated
2017-07-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

middle and advanced squamous cells esophageal cancer

Interventions

Experimental group:Apatinib and sequential chemoradiotherapy
control group:sequential chemoradiotherapy

Sponsors

Nanchong Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Aged between 18-70 years; 2. Making a definite diagnosis of squamous cells esophageal cancer in pathology; 3. The stages between II/III stage; 4. At the beginning of treatment; 5. The size of tumour to be able to measured; 7. ECOG=2 scores. 8. Except survival time at least 6 months; 9. WBC=4×10^9/L, ANC=2×10^9/L, HGB =90 g/L, PLT=90×10^9/L; 10. Liver and kidney function ALT, AST, STBS, CR50%, DLCO measured value/predicted value>80%.

Exclusion criteria

Exclusion criteria: 1. Having remote cancer transfer; 2. Having already received surgeryradiotherapychemotherapyor target treat; 3. Be diagnosed in other cancer in 5 years (except cervical carcinoma in situbasal cell carcinoma in skinUrothelial carcinomaearly stage prostatic carcinoma); 4. Be received other medicinal trials in 1 mouth; 5. Pregnant or?breast-feedor refuse to receive birth control duration of Therapy women; 6. Having serious?allergy history; 7. Having Serious Lung or heart disease; 8. Refusing or can not sign informed consent; 9. Misusing of drugs or alcohol.

Design outcomes

Primary

MeasureTime frame
ORR;PFS;

Countries

China

Contacts

Public ContactHu Xingsheng

Nanchong Central Hospital

137666745@qq.com+86 18080343730

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026