JPRN-UMIN000010721
Recruiting
Phase 2
Assessment of efficacy and safety of continouation maintenance therapy with gemcitabine after cisplatin-gemcitabine induction chemotherapy in advanced squamous cell lung cancer (KTORG1302) - Assessment of efficacy and safety of CDDP+GEM followed by GEM in advanced squamous cell lung cancer
Kyoto Thoracic Oncology Research Group (KTORG)0 sites60 target enrollmentMay 15, 2013
Conditionssquamous cell lung cancer
Overview
- Phase
- Phase 2
- Intervention
- Not specified
- Conditions
- squamous cell lung cancer
- Sponsor
- Kyoto Thoracic Oncology Research Group (KTORG)
- Enrollment
- 60
- Status
- Recruiting
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- Not provided
Exclusion Criteria
- •1\) Patients with histologically proven non\-squamous cell lung cancer 2\) Recognized ILD or pulmonary fibrosis on X\-rays 3\) Pleural effusion, peritoneal fluid and pericardial fluid that need treatment 4\) Superior vena cava syndrome 5\) Symptomatic brain metastasis 6\) Active concomitant malignancy 7\) Prior therapy with gemcitabine 8\) Diabetes and hypertension that cannot be controlled 9\) Liver cirrhosis 10\) Symptomatic or asymptomatic but treated heart disease 11\) Severe infectious disease 12\) Pregnant women, possibly pregnant women, wishing to become pregnant 13\) Serious drug hypersensitivity or a history of drug allergy 14\) Refusal of supportive care such as blood transfusion 15\) Bleeding tendency 16\) Other conditions not suitable for this study
Outcomes
Primary Outcomes
Not specified
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