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A Retrospective Study of Toxicity and Outcome of High Dose Chemotherapy With Autologous Stem Cell Transplant in Patients With Hodgkin Lymphoma (HL).
This study is currently recruiting participants.
Verified by Royal Marsden NHS Foundation Trust, March 2006
Sponsored by: Royal Marsden NHS Foundation Trust
Information provided by: Royal Marsden NHS Foundation Trust
ClinicalTrials.gov Identifier: NCT00301314
  Purpose

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 retrospectve review, we aim to analyse outcome and determine independent prognostic factors which would correlate with the long−term outcome of patiensts 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 Intervention
Hodgkin Lymphoma
Procedure: Autologous stem cell transplant

MedlinePlus related topics: Hodgkin's Disease Lymphoma
U.S. FDA Resources
Study Type: Observational
Study Design: Longitudinal, Defined Population, Retrospective Study
  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Criteria

Inclusion Criteria:

  • a) Age over 18 b) Patients with Hodgkin Lymphoma who have received an autologous stem cell transplant c) Informed written consent

Exclusion Criteria:

  • a) Medical or psychiatric conditions that compromise the patient’s ability to give informed consent b) HIV positive or AIDS related lymphoma
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00301314

Contacts
Contact: Bhawna Sirohi, MBBS, MD 0044 208 661 3115 bhawna.sirohi@rmh.nhs.uk

Locations
United Kingdom, Surrey
Royal Marsden NHS trust Recruiting
Sutton, Surrey, United Kingdom, SM2 5PT
Contact: Bhawna Sirohi, MBBS, MD     0044 208 661 3115     bhawna.sirohi@rmh.nhs.uk    
Contact: Jacqui Oates     00442086613279     jacqui.oates@rmh.nhs.uk    
Sub-Investigator: Bhawna Sirohi, MBBs, MD            
Sponsors and Collaborators
Royal Marsden NHS Foundation Trust
Investigators
Principal Investigator: David Cunningham, FRCP Royal Marsden NHS Foundation Trust
  More Information

Study ID Numbers: 2655
Study First Received: March 9, 2006
Last Updated: October 12, 2006
ClinicalTrials.gov Identifier: NCT00301314  
Health Authority: United Kingdom: National Health Service

Study placed in the following topic categories:
Lymphatic Diseases
Hodgkin's disease
Immunoproliferative Disorders
Hodgkin lymphoma, adult
Lymphoproliferative Disorders
Hodgkin Disease
Lymphoma

Additional relevant MeSH terms:
Neoplasms
Neoplasms by Histologic Type
Immune System Diseases

ClinicalTrials.gov processed this record on January 15, 2009