Journal of Clinical Oncology, Vol 17, Issue 10
(October), 1999: 3101-3109
© 1999 American Society for Clinical Oncology
High-Dose Therapy and Autologous Stem-Cell Transplantation for Adult Patients With Hodgkin's Disease Who Do Not Enter Remission After Induction Chemotherapy: Results in 175 Patients Reported to the European Group for Blood and Marrow Transplantation
John W. Sweetenham,
Angelo M. Carella,
Golnaz Taghipour,
David Cunningham,
Robert Marcus,
Aldo Della Volpe,
David C. Linch,
Norbert Schmitz,
Anthony H. Goldstone,
on Behalf of the Lymphoma Working Party of the European Group for Blood and Marrow Transplantation
From the CRC Wessex Medical Oncology Unit, University of Southampton, Southampton; Department of Clinical Haematology, University College Hospital, and Royal Marsden Hospital, London; Department of Haematology, Addenbrooke's Hospital, Cambridge, United Kingdom; Ematologia Ed Autotrapianto di Midollo, Ospedale S Martino, Genova, and Centro Trapianti di Midollo, Ospedale Maggiore di Milano, Milan, Italy; and Second Department of Internal Medicine, Christian Albrechts University, Kiel, Germany.
Address reprint requests to John Sweetenham, MD, CRC Wessex Medical Oncology Unit, University of Southampton, Southampton General Hospital, Tremona Road Southampton SO16 6YD, United Kingdom; email jws{at}soton.ac.uk
PURPOSE: To investigate the results of high-dose therapy and autologous stem-cell transplantation (ASCT) in adults with Hodgkin's disease who do not enter remission after induction therapy, to determine overall survival (OS) and progression free survival (PFS), and to identify prognostic factors.
PATIENTS AND METHODS: A retrospective analysis of 175 patients reported to the European Group for Blood and Marrow Transplantation between November 1979 and October 1995. One hundred were male and 75 were female, with a median age of 26.5 years. Responses to first-line therapy were defined as progressive disease (PD) in 88 and stable/minimally responsive disease (SD/MR) in 87. Seventy-five patients received ASCT after failure of one induction regimen. Second-line therapy was given to the remaining 100 patients. Response to second-line therapy was PD in 34 and SD/MR in 66. OS and PFS rates were determined, and prognostic factors were investigated using univariate and multivariate analyses.
RESULTS: Responses to high-dose therapy and ASCT were complete response (30%), partial response (28%), no response (14%), PD (14%), and toxic death (14%). Actuarial 5-year OS and PFS rates were 36% and 32%, respectively. In univariate analysis for PFS and OS, adverse factors were use of a second-line chemotherapy regimen and interval of more than 18 months between diagnosis and ASCT. In multivariate analysis, the interval between diagnosis and ASCT maintained prognostic significance for OS. Response to the chemotherapy regimen given immediately before ASCT had no predictive value.
CONCLUSION: High-dose therapy and ASCT is an effective treatment strategy for patients with Hodgkin's disease for whom induction chemotherapy fails. Outcome was equivalent for those with obvious PD or SD/MR in response to the regimen given immediately before high-dose therapy. Prospective randomized studies are required to compare this approach with conventional-dose salvage therapy.

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