The Role of Autologous Stem Cell Transplantation in the Treatment of Diffuse Large B-Cell Lymphoma

Diffuse large B-cell non-Hodgkin’s lymphoma (DLBCL) accounting for approximately 30% of new lymphoma diagnoses in adult patients. Complete remissions (CRs) can be achieved in 45% to 55% of patients and cure in approximately 30–35% with anthracycline-containing combination chemotherapy. The ageadjust...

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Main Authors: Marco Gunnellini, Rita Emili, Stefano Coaccioli, Anna Marina Liberati
Format: Article
Language:English
Published: Hindawi Limited 2012-01-01
Series:Advances in Hematology
Online Access:http://dx.doi.org/10.1155/2012/195484
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spelling doaj-7ea684e7b63743e2b708b49a5d71d10d2021-07-02T09:53:53ZengHindawi LimitedAdvances in Hematology1687-91041687-91122012-01-01201210.1155/2012/195484195484The Role of Autologous Stem Cell Transplantation in the Treatment of Diffuse Large B-Cell LymphomaMarco Gunnellini0Rita Emili1Stefano Coaccioli2Anna Marina Liberati3Department of Transplant Oncohematology, Perugia University, S. Maria, Terni, ItalyDepartment of Transplant Oncohematology, Perugia University, S. Maria, Terni, ItalyFaculty of Medicine, Perugia University, S. Maria, Terni, ItalyDepartment of Transplant Oncohematology, Perugia University, S. Maria, Terni, ItalyDiffuse large B-cell non-Hodgkin’s lymphoma (DLBCL) accounting for approximately 30% of new lymphoma diagnoses in adult patients. Complete remissions (CRs) can be achieved in 45% to 55% of patients and cure in approximately 30–35% with anthracycline-containing combination chemotherapy. The ageadjusted IPI (aaIPI) has been widely employed, particularly to “tailor” more intensive therapy such as high-dose therapy (HDT) with autologous hemopoietic stem cell rescue (ASCT). IPI, however, has failed to reliably predict response to specific therapies. A subgroup of young patients with poor prognosis exists. To clarify the role of HDT/ASCT combined with rituximab in the front line therapy a longer follow-up and randomized studies are needed. The benefit of HDT/ASCT for refractory or relapsed DLBCL is restricted to patients with immunochemosensitive disease. Currently, clinical and biological research is focused to improve the curability of this setting of patients, mainly young.http://dx.doi.org/10.1155/2012/195484
collection DOAJ
language English
format Article
sources DOAJ
author Marco Gunnellini
Rita Emili
Stefano Coaccioli
Anna Marina Liberati
spellingShingle Marco Gunnellini
Rita Emili
Stefano Coaccioli
Anna Marina Liberati
The Role of Autologous Stem Cell Transplantation in the Treatment of Diffuse Large B-Cell Lymphoma
Advances in Hematology
author_facet Marco Gunnellini
Rita Emili
Stefano Coaccioli
Anna Marina Liberati
author_sort Marco Gunnellini
title The Role of Autologous Stem Cell Transplantation in the Treatment of Diffuse Large B-Cell Lymphoma
title_short The Role of Autologous Stem Cell Transplantation in the Treatment of Diffuse Large B-Cell Lymphoma
title_full The Role of Autologous Stem Cell Transplantation in the Treatment of Diffuse Large B-Cell Lymphoma
title_fullStr The Role of Autologous Stem Cell Transplantation in the Treatment of Diffuse Large B-Cell Lymphoma
title_full_unstemmed The Role of Autologous Stem Cell Transplantation in the Treatment of Diffuse Large B-Cell Lymphoma
title_sort role of autologous stem cell transplantation in the treatment of diffuse large b-cell lymphoma
publisher Hindawi Limited
series Advances in Hematology
issn 1687-9104
1687-9112
publishDate 2012-01-01
description Diffuse large B-cell non-Hodgkin’s lymphoma (DLBCL) accounting for approximately 30% of new lymphoma diagnoses in adult patients. Complete remissions (CRs) can be achieved in 45% to 55% of patients and cure in approximately 30–35% with anthracycline-containing combination chemotherapy. The ageadjusted IPI (aaIPI) has been widely employed, particularly to “tailor” more intensive therapy such as high-dose therapy (HDT) with autologous hemopoietic stem cell rescue (ASCT). IPI, however, has failed to reliably predict response to specific therapies. A subgroup of young patients with poor prognosis exists. To clarify the role of HDT/ASCT combined with rituximab in the front line therapy a longer follow-up and randomized studies are needed. The benefit of HDT/ASCT for refractory or relapsed DLBCL is restricted to patients with immunochemosensitive disease. Currently, clinical and biological research is focused to improve the curability of this setting of patients, mainly young.
url http://dx.doi.org/10.1155/2012/195484
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