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A Retrospective Study of Toxicity and Outcome of High Dose Chemotherapy With Autologous Stem Cell Transplant in Patients With Non-Hodgkin Lymphoma (NHL).
This study is currently recruiting participants.
Verified by Royal Marsden NHS Foundation Trust, March 2006
First Received: March 9, 2006   Last Updated: October 12, 2006   History of Changes
Sponsored by: Royal Marsden NHS Foundation Trust
Information provided by: Royal Marsden NHS Foundation Trust
ClinicalTrials.gov Identifier: NCT00301288
  Purpose

Patients with aggressive Non−Hodgkin−lymphoma treated at first diagnosis with chemotherapy alone or combined chemoradiotherapy can achieve high response rates. However, patients with relapsed lymphoma still have a poor prognosis. Highdose chemotherapy (HDCT) followed by autologous stem cell transplantation (ASCT) is the treatment of choice for these patients. An ASCT allows patients to recieve much higher doses of chemotherapy than usual, to improve the chances of curing the disease. The high−dose of chemotherapy destroys the cells in the patients bone marow and then the patients own cells from either the bone marrow or peripheral blood are used to rescue the patient from intensive treatment. High−dose chemotherapy with autologous stem cell (either bone marrow or peripheral blood) transplantation is used in the treatment of Intermediate/High grade NHL with poor risk disease and in second remission at the Royal Marsden Hospital.

The purpose of the present analysis is to determine independent prognostic factors correlated with the long−term outcome of patients with NHL who received an ASCT between January 1991 and June 2005. 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. This will include patients treated at the royal Marsden Hospital only.


Condition Intervention
Non-Hodgkins Lymphoma
Procedure: Autologous stem cell transplant

MedlinePlus related topics: 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 Non-Hodgkin’s Lymphoma who have received an autologous stem cell transplant in the past.

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: NCT00301288

Contacts
Contact: Bhawna Sirohi, MBBS, MD 0044 208 661 3115 bhawna.sirohi@rmh.nhs.uk
Contact: Jacqui Oates 0044 2086613279 jacqui.oates@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    
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

No publications provided

Study ID Numbers: 2657
Study First Received: March 9, 2006
Last Updated: October 12, 2006
ClinicalTrials.gov Identifier: NCT00301288     History of Changes
Health Authority: United Kingdom: National Health Service

Study placed in the following topic categories:
Lymphoma, Small Cleaved-cell, Diffuse
Lymphatic Diseases
Immunoproliferative Disorders
Lymphoproliferative Disorders
Lymphoma, Non-Hodgkin
Lymphoma

Additional relevant MeSH terms:
Lymphatic Diseases
Neoplasms
Immunoproliferative Disorders
Neoplasms by Histologic Type
Immune System Diseases
Lymphoproliferative Disorders
Lymphoma, Non-Hodgkin
Lymphoma

ClinicalTrials.gov processed this record on May 07, 2009