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Endostar Continued Pumping Into Vein Combining With Gemcitabine-Carboplatin to Treat Non-Small Cell Lung Cancer (NSCLC)

Phase 2
Conditions
Non-small Cell Lung Cancer
Interventions
Drug: Gemcitabine,Carboplatin,Endostar
Drug: 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
Inclusion Criteria
  1. Histologically or cytologically diagnosed NSCLC;

  2. primary treatment,inoperable stage III/IV NSCLC;

  3. Age of 18-70years; Gender Not Required;

  4. 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;

  5. ECOG PS 0-2,Life expectancy ≥ 3 months; endure more than two cycle chemotherapy;

  6. 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);

  7. No history of serious drug allergy;

  8. Informed consent should be obtained before treatment.

Exclusion Criteria
  1. Symptomatic brain metastases with cognitive disorder,bone metastases with complications;
  2. Major organ dysfunction and Serious Heart Disease( congestive heart-failure,incontrollable high-risk arrhythmia,unstable angina, valvular disease, myocardial infarct and Resistant hypertension,);
  3. Serious complications and investigator consider it is unsuited enrolling;
  4. Pregnant or lactating women;
  5. Allergic to research drug;
  6. participating in other experimental trials and receive the treatment in four weeks;
  7. The position that is for observing curative effect have a radiotherapy.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Endostar -Continued Pumping into+GCGemcitabine,Carboplatin,EndostarEndostar that is Continued Pumping into vein Combining With Gemcitabine -Carboplatin
Endostar -injecting into +GCGemcitabine(G) Carboplatin(C) EndostarEndostar that is injecting into vein with Gemcitabine -Carboplatin
GCGemcitabine(G) Carboplatin(C)Gemcitabine -Carboplatin
Primary Outcome Measures
NameTimeMethod
Progression free survival (PFS)two years
Secondary Outcome Measures
NameTimeMethod
The level change of CECs,VEGF,TSP-1,VEGFR,P1GF,MVD in blood.two years
adverse reactiontwo 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

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