A Retrospective Study of Toxicity and Outcome of High Dose Chemotherapy With Autologous Stem Cell Transplant in Patients With Hodgkin Lymphoma (HL).

Sponsor
Royal Marsden NHS Foundation Trust (Other)
Overall Status
Completed
CT.gov ID
NCT00301314
Collaborator
(none)
1

Study Details

Study Description

Brief Summary

The majority of patients with Hodgkin Lymphoma (HL)are cured with radiation therapy and/or combination chemotherapy. However, patients who relapse after attaining a complete remission with chemotherapy and those with primary refractory disease have a poor outcome with conventional chemotherapy regimens. Treatment results with standard-dose second-line regimens produce low complete remission rates and minimal survival benefit. Single institution studies have shown better outcome after autologous stem cell transplant in this group of patients when compared to historical controls receiving conventional treatment. In this retrospective review, we aim to analyze outcome and determine independent prognostic factors which would correlate with the long-term outcome of patients with HL who received an autologous stem cell transplant in the past at the Royal Marsden Hospital Eligible patients (those on current-follow-up) identified from the transplant database will be eligible for the study.

Accrual of eligible patients currently under follow-up will be performed in clinic at the time of next appointment. All patients accrued will give informed consent to participate in the study for retrospective case note review, after discussion with a study investigator and after receiving a study information sheet. The results of the analysis will be published in a peer-reviewed medical journal.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Autologous stem cell transplant

Study Design

Study Type:
Observational
Time Perspective:
Retrospective

Outcome Measures

Primary Outcome Measures

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
      1. Age over 18 b) Patients with Hodgkin Lymphoma who have received an autologous stem cell transplant c) Informed written consent
    Exclusion Criteria:
      1. Medical or psychiatric conditions that compromise the patient's ability to give informed consent b) HIV positive or AIDS related lymphoma

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Royal Marsden NHS trust Sutton Surrey United Kingdom SM2 5PT

    Sponsors and Collaborators

    • Royal Marsden NHS Foundation Trust

    Investigators

    • Principal Investigator: David Cunningham, FRCP, Royal Marsden NHS Foundation Trust

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    , ,
    ClinicalTrials.gov Identifier:
    NCT00301314
    Other Study ID Numbers:
    • 2655
    First Posted:
    Mar 10, 2006
    Last Update Posted:
    Jan 12, 2010
    Last Verified:
    Jan 1, 2010
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jan 12, 2010