Endostar Continued Pumping Into Vein Combining With Gemcitabine-Carboplatin to Treat Non-Small Cell Lung Cancer (NSCLC)
- Conditions
- Non-small Cell Lung Cancer
- Interventions
- Drug: Gemcitabine,Carboplatin,EndostarDrug: Gemcitabine(G) Carboplatin(C)
- Registration Number
- NCT01549093
- Lead Sponsor
- Hunan Province Tumor Hospital
- Brief Summary
The purpose of this study is to determine whether Endostar with Gemcitabine-Carboplatin are more effective than Gemcitabine-Carboplatin alone in the treatment of Non-Small Cell Lung Cancer (NSCLC),and about Endostar ,Compared with intravenous, Continued vein-pumping maby is a more effective way.
- Detailed Description
Endostar have anti-tumor activity by against vascular endothelial growth factor for initial treatment. This study was designed to evaluate the safety and efficacy of Endostar Continued vein-pumping Combining with Gemcitabine-Carboplatin (GC)chemotherapy in patients with NSCLC,and seeking for more effective injection.
Methods:
In this randomized, open label, 90 patients are planned to be enrolled at random into 3 arms(1:1:1): Experimental: Endostar -Continued Pumping into+Gemcitabine-Carboplatin(GC),Active Comparator: Endostar -injecting into +Gemcitabine-Carboplatin(GC),Active Comparator: Gemcitabine-Carboplatin(GC),
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 90
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Histologically or cytologically diagnosed NSCLC;
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primary treatment,inoperable stage III/IV NSCLC;
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Age of 18-70years; Gender Not Required;
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Adequate hematologic, renal, and hepatic function ,Specific index as follows:
liver function: S-Bilirubin ≤1.5 ULN ; Transaminase≤2 ULN. renal function: S-Creatinine ≤1.2 ULN; blood urea nitrogen ≤1.2 ULN . ULN: upper normal limit. Marrow Hemopoietic Function: WBC≥4.0×10^9/l, ANC≥2.0×10^9/l platelet count ≥100×10^9/l, Hb≥100 g/l;
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ECOG PS 0-2,Life expectancy ≥ 3 months; endure more than two cycle chemotherapy;
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The patients have explicit lung tumor lesions and the lesions were measurable; (According to the standard of RECIST1.1, they should have at least one of accurately measurable lesions with the largest diameter ≥ 10mm by spiral CT, MRI);
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No history of serious drug allergy;
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Informed consent should be obtained before treatment.
- Symptomatic brain metastases with cognitive disorder,bone metastases with complications;
- Major organ dysfunction and Serious Heart Disease( congestive heart-failure,incontrollable high-risk arrhythmia,unstable angina, valvular disease, myocardial infarct and Resistant hypertension,);
- Serious complications and investigator consider it is unsuited enrolling;
- Pregnant or lactating women;
- Allergic to research drug;
- participating in other experimental trials and receive the treatment in four weeks;
- The position that is for observing curative effect have a radiotherapy.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Endostar -Continued Pumping into+GC Gemcitabine,Carboplatin,Endostar Endostar that is Continued Pumping into vein Combining With Gemcitabine -Carboplatin Endostar -injecting into +GC Gemcitabine(G) Carboplatin(C) Endostar Endostar that is injecting into vein with Gemcitabine -Carboplatin GC Gemcitabine(G) Carboplatin(C) Gemcitabine -Carboplatin
- Primary Outcome Measures
Name Time Method Progression free survival (PFS) two years
- Secondary Outcome Measures
Name Time Method The level change of CECs,VEGF,TSP-1,VEGFR,P1GF,MVD in blood. two years adverse reaction two years Overall survival (OS) two years Time to progression(TTP) two years Clinical benefit rate (CBR) two years
Trial Locations
- Locations (1)
HuNan province tumor hospital
🇨🇳Changsha, Hunan, China