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Phase II trial of paclitaxel (T) vs Irinotecan(I) in patients with extensive disease (ED) small cell lung cancer (SCLC) as 2nd line chemotherapy

Not Applicable
Recruiting
Conditions
Neoplasms
Registration Number
KCT0003330
Lead Sponsor
Chung-Ang Univerisity Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
136
Inclusion Criteria

1) Histologically or cytologically diagnosed dilated stage small cell lung cancer patient
2) Patients who were treated with etoposide / platinum combination therapy as a first-line treatment and who had more than partial response (PR) and sustained more than 90 days. However, it is a rule to keep it for more than 90 days, but it is also possible to register patients who are kept for more than 60 days.
3) In the presence of brain metastases with neurological symptoms, previous radiation therapy or surgical treatment for brain metastases was neurologically stable (no progressive neurological symptoms, and steroid therapy was discontinued). Radiation therapy The researcher has determined that the toxicity of
4) When radiation therapy is applied to areas other than the brain, it can be selected when the scope of irradiation does not include target lesions
5) Appropriate bone marrow, liver, new function
Serum creatinine ? Normal upper limit of each organ (UNL)
Serum transaminase = UNL x 2.0 (if there is liver damage ? UNL x 5
Serum bilirubin ? UNL x 1.5
neutrophil count ? 1,500 / uL, platelets ? 100,000 / uL
6) If there is more than one measurable lesion based on RECIST criteria
7) 20 years old or older
8) Eastern Cooperative Oncology Group (ECOG) Activity 0-2
9) Have obtained written consent based on the guidelines of each institutional clinical trial committee

Exclusion Criteria

1) Patients with brain metastases whose symptoms are not adequately controlled
2) Patients with significant infectious disease to which parenteral antibiotics should be administered
3) diarrhea patients whose symptoms are not adequately controlled
4) Chronic inflammatory bowel disease whose symptoms are not adequately controlled
5) Patients with bowel obstruction, bowel obstruction
6) Patients with interstitial pneumonia or pulmonary fibrosis
7) Patients with dialysis
8) Pregnant or potentially pregnant women and lactating women
9) Patients receiving Atazanavir Sulfate
10) Patients who have a history of hypersensitivity reactions to xylitol or its components. Patients with a history of severe hypersensitivity to other drugs containing Cremophor® EL (polyoxyethylated castor oil)
11) Large amount of ascites, pleural effusion
12) Patients receiving St. John's Wort

Study & Design

Study Type
Interventional Study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Response rates between two group
Secondary Outcome Measures
NameTimeMethod
Overall survival between two group;Progression free survival between two group;Toxicity between two group
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