A Retrospective Chart Review to Describe the Rate of Neutropenic Sepsis in Patients With Non-Small Cell Lung Cancer Treated With Single-Agent Docetaxel and Associated Resource Use in the UK
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Non-Small Cell Lung Cancer
- Sponsor
- Hoffmann-La Roche
- Enrollment
- 120
- Locations
- 7
- Primary Endpoint
- Percentage of Participants Receiving Single-Agent Docetaxel Chemotherapy for Treatment of Relapsed Non-Small Cell Lung Cancer (NSCLC) with an Episode of Neutropenic Sepsis (NS) with an Absolute Neutrophil Count of Less Than 1.0 x 10^9/L
- Status
- Completed
- Last Updated
- 8 years ago
Overview
Brief Summary
This is a multi-center retrospective observational research study collecting data for participants initiated on docetaxel for the treatment of relapsed non-small cell lung cancer (NSCLC) up to 6 years before start of data collection and who have completed/stopped docetaxel treatment at least 30 days prior to data collection. The primary goal of this study is to describe the percentage of participants with at least one neutropenic sepsis (NS) episode following initiation of treatment with single-agent docetaxel. Data will be collected until end of docetaxel treatment plus an additional 30 days to allow for presentation with toxicity.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Diagnosed with locally advanced or metastatic (stage Ill or IV) non-small cell lung cancer (NSCLC)
- •Relapsed disease following, or unable to tolerate, at least one line of prior chemotherapy
- •Initiated on single-agent docetaxel up to a maximum of 6 years prior to date of collection
- •Aged 18 years at date of first docetaxel dose
- •Completed or stopped treatment with docetaxel at least 30 days prior to date of data collection
Exclusion Criteria
- •Receiving docetaxel in an interventional clinical trial
- •For whom no details of absolute neutrophil count are recorded
Outcomes
Primary Outcomes
Percentage of Participants Receiving Single-Agent Docetaxel Chemotherapy for Treatment of Relapsed Non-Small Cell Lung Cancer (NSCLC) with an Episode of Neutropenic Sepsis (NS) with an Absolute Neutrophil Count of Less Than 1.0 x 10^9/L
Time Frame: Up to 6 years
Secondary Outcomes
- Frequency with which Participants Attend Hospital for Management of Specified Hematological Docetaxel-Related Toxicities, Including Anemia, Thrombocytopenia, Neutropenia, Neutropenic Infection and Pancytopenia(Up to 6 years)
- Number of Episodes of Neutropenic Sepsis (NS) with an Absolute Neutrophil Count of Less Than 1.0 x 10^9/L(Up to 6 years)
- Percentage of Participants with Docetaxel-Related Hematological Toxicities, Including Anemia, Thrombocytopenia, Neutropenia, Neutropenic Infection and Pancytopenia(Up to 6 years)
- Number of Episodes of NS Associated with Death Attributable to NS(Up to 6 years)
- Percentage of Participants Receiving Single-Agent Docetaxel Chemotherapy for Treatment of Relapsed Non-Small Cell Lung Cancer (NSCLC) with an Episode of Neutropenic Sepsis (NS) with an Absolute Neutrophil Count of Less Than 0.5 x 10^9/L(Up to 6 years)
- Percentage of Deaths Associated with the Occurrence of an NS Event(Up to 6 years)
- Number of Episodes of NS with an Absolute Neutrophil Count of Less Than 0.5 x 10^9/L(Up to 6 years)