Status:

COMPLETED

Preoperative Twice Daily Chemoradiation in Addition to Chemotherapy Prior to Surgery in Stage III Non-Small Cell Lung Cancer (NSCLC)

Lead Sponsor:

Heidelberg University

Collaborating Sponsors:

University Hospital Muenster

Lung Clinic Hemer

Conditions:

Non-Small Cell Lung Cancer

Eligibility:

All Genders

18-69 years

Phase:

PHASE3

Brief Summary

Patients are randomized to (arm A) 3 cycles of cisplatin/etoposide, followed by hyperfractionated radiotherapy (hfRT)with concurrent carboplatin and vindesine then surgery and, if no or R1/2-resection...

Detailed Description

Patients are randomized to (arm A) 3 cycles of cisplatin 55 mg/m2 (d 1 + 4)/etoposide 100 mg/m2 (d 1-4), followed by hyperfractionated radiotherapy (hfRT; 45 Gy, 2x1.5 Gy/d) with concurrent carboplati...

Eligibility Criteria

Inclusion

  • non-small cell lung cancer proven by histology
  • stage IIIA / stage IIIB
  • mediastinoscopy
  • performance score ECOG 0,1
  • predicted postoperative FEV 1 \> 1.0 l

Exclusion

  • small cell lung cancer
  • cardiac disability (NYHA III/IV)
  • prior radio- or chemotherapy
  • pregnancy
  • other malignancy

Key Trial Info

Start Date :

October 1 1995

Trial Type :

INTERVENTIONAL

End Date :

September 1 2005

Estimated Enrollment :

500 Patients enrolled

Trial Details

Trial ID

NCT00176137

Start Date

October 1 1995

End Date

September 1 2005

Last Update

April 22 2008

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