advanced squamous non-small-cell lung cancer
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) pathologically or cytologically diagnosed as squamous NSCLC 2) clinical stage IIIB, IV or relapse 3) ECOG PS of 0-1 4) expectation of at least 3 months of survival after study therapy 5) existence of measurable lesion 6) capability of oral intake 7) adequate organ function 8) written informed consent given
Exclusion criteria
Exclusion criteria: 1) history of pyrimidine-based chemotherapy 2) symptomatic brain metastasis (asymptomatic cases after treatments are allowed) 3) fluid retention that needs to be controlled 4) watery diarrhea 5) severe comorbidities 6) active cancers in other organs 7) existence and/or willing to pregnancy 8) psychological disorder incapable of entry for the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| PFS measured from start of the maintenance therapy | — |
Secondary
| Measure | Time frame |
|---|---|
| OS, PFS measured from the enrollment, response rate, disease control rate in the induction therapy, safety | — |
Countries
Japan
Contacts
Hamamatsu Univ. School of Medicine Department of clinical oncology