Neutropenic Sepsis in Patients With Non-Small Cell Lung Cancer Treated With Single-Agent Docetaxel and Associated Resource Use in the UK

  • Cancer
  • Lung Cancer
  • Non-Small Cell Lung Cancer (NSCLC)
Please note that the recruitment status of the trial at your site may differ from the overall study status because some study sites may recruit earlier than others.
Trial Status:

Completed

This trial runs in
Cities
  • Bristol
  • Cardiff
  • London
  • Maidstone
  • Oxford
  • Truro
  • Wakefield
Trial Identifier:

NCT02658747 ML30033

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      The source of the below information is public registry websites such as ClinicalTrials.gov, EuClinicalTrials.eu, ISRCTN.com, etc.. It has been summarised and edited into simpler language. For more information about this clinical trial see the For Expert tab on the specific ForPatients page or follow these links to https://clinicaltrials.gov and/or https://euclinicaltrials.eu and/or https://www.isrctn.com.

      The below information is taken directly from public registry websites such as ClinicalTrials.gov, EuClinicalTrials.eu, ISRCTN.com, etc., and has not been edited.

      Results Disclaimer

      Trial 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.

      Hoffmann-La Roche Sponsor
      N/A Phase
      NCT02658747, ML30033 Trial Identifier
      No intervention Treatments
      Non-Small Cell Lung Cancer Condition
      Official Title

      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

      Eligibility Criteria

      All Gender
      ≥ 18 Years Age
      No Healthy Volunteers
      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

      For the latest version of this information please go to www.forpatients.roche.com

       

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