The purpose of this study was to evaluate the safety and efficacy of neoadjuvant concurrent chemoradiation with weekly docetaxel/cisplatin in patients with resectable IIIA-N2 NSCLC.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
50
weekly docetaxel/cisplatin combined with radiation
chemoradiation
Peking university people's hospital
Beijing, Beijing Municipality, China
RECRUITINGdownstage rate of mediastinal lymph nodes
Time frame: 8 weeks
overall survival
Time frame: 5y
Disease-free survival
Time frame: 5y
resection rate
Time frame: 12 weeks
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.