Overview

Phase II Study of Docetaxel Plus CDDP for NSCLC Stage III

Status:
Completed
Trial end date:
2010-03-01
Target enrollment:
0
Participant gender:
All
Summary
To assess the overall response rate to docetaxel plus CDDP as neoadjuvant chemotherapy prior to surgery, followed by adjuvant docetaxel plus CDDP in chemonaive patients NSCLC Stage IIIa and IIIb.
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
National Taiwan University Hospital
Treatments:
Cisplatin
Docetaxel
Criteria
Inclusion Criteria:

- Histologically or cytologically confirmed NSCLC, respectable NSCLC stage IIIa T1-2 N2
or or unresectable stage IIIb 2.KPS>70%
3.Hb>10g/dl,ANC>2.0x109/L,Plt.>100x109/L4.T-bil.<1xULN,creatinine<1xULN,creatinine
clearance >60 ml/min,GPT/GOT<2.5xULN,ALP<5xULN

Exclusion Criteria:

- 1.Brain meta.2..Prior surgery,R/T, C/t or immunotherapy for NSCLC