Skip to main content
Clinical Trials/NCT01494558
NCT01494558
Completed
Phase 2

Phase 3 Study of Etoposide, Cisplatin, and Radiotherapy Versus Paclitaxel, Carboplatin and Radiotherapy in Patients With Unresectable Locally Advanced, Stage III Non-Small Cell Lung Cancer

Chinese Academy of Medical Sciences0 sites200 target enrollmentMay 2007

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Non-Small Cell Lung Cancer
Sponsor
Chinese Academy of Medical Sciences
Enrollment
200
Primary Endpoint
Overall Survival
Status
Completed
Last Updated
14 years ago

Overview

Brief Summary

Cisplatin-based combination chemotherapy given concurrently with radiotherapy is the standard of care for patients with inoperable stage III NSCLC. The most common chemotherapeutic agents used concurrently with radiotherapy have been vinorelbine, vinblastine, and etoposide in conjunction with cisplatin or weekly paclitaxel and carboplatin. No randomized phase III trials of concurrent chemoradiotherapy have shown the superiority of one chemotherapy regimen over another. The clinical trial is to compare radiotherapy concurrently with PE (etoposide and cisplatin) and PC (paclitaxel and carbplatin) for local advanced NSCLC (stage IIIA/IIIB). It is a randomized, multicenter, open labeled phase III clinical trial. All patients receive conformal radiotherapy or intensity modulated radiotherapy with conventional fraction. The chemotherapy regimens are PE (etoposide 50mg/m2 d1-5, 29-33 and cisplatin 50mg/m2 d1,8,29 and 36 29-33 ) and PC (paclitaxel 45mg/m2 weekly over 1hour and carbplatin AUC =2mg/mL/min over 30min weekly). The primary purpose is to evaluate objective response rate, complications, progression-free survival, overall survival. The second purpose is to evaluate quality of life and cost.

Registry
clinicaltrials.gov
Start Date
May 2007
End Date
August 2011
Last Updated
14 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Luhua Wang

Chairman of Thoracic Group, Clinical Professor, Radiation Oncology Department, Cancer Hospital&Institute

Chinese Academy of Medical Sciences

Eligibility Criteria

Inclusion Criteria

  • Inoperable stage IIIA/IIIB NSCLC proved by pathology or cytology
  • Age 18 to 75, ECOG ≤ 2, lose weight \<10% during 6 months
  • No serious diseases of important organs
  • Chest CT in recently 4 weeks
  • No other tumor disease except stage I cervical cancer or cutaneous basal cell carcinoma
  • Sign consent
  • Measurable lesion

Exclusion Criteria

  • Pretreatment radiotherapy or chemotherapy
  • Pregnant or lactation woman
  • Serious diseases (include uncontrolled diabetes and infection) of important organs
  • Join in other clinical trial

Outcomes

Primary Outcomes

Overall Survival

Time Frame: 2 years

Secondary Outcomes

  • Progression Free Survival(2 years)

Similar Trials