Cargando…
Improving Outcomes After Allogeneic Hematopoietic Cell Transplantation for Hodgkin Lymphoma in the Brentuximab Vedotin Era
Allogeneic hematopoietic cell transplantation (allo HCT) remains a valuable alternative for relapsed/refractory (R/R) Hodgkin lymphoma (HL). Data on allo HCT outcomes in the era of new HL therapies are needed. We evaluated 72 R/R HL patients who received reduced intensity conditioning (RIC) allo HCT...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5415418/ https://www.ncbi.nlm.nih.gov/pubmed/28134921 http://dx.doi.org/10.1038/bmt.2016.357 |
_version_ | 1783233515339382784 |
---|---|
author | Hegerova, Livia Cao, Qing Lazaryan, Aleksander McClune, Brian L. Weisdorf, Daniel J. Brunstein, Claudio G. Bachanova, Veronika |
author_facet | Hegerova, Livia Cao, Qing Lazaryan, Aleksander McClune, Brian L. Weisdorf, Daniel J. Brunstein, Claudio G. Bachanova, Veronika |
author_sort | Hegerova, Livia |
collection | PubMed |
description | Allogeneic hematopoietic cell transplantation (allo HCT) remains a valuable alternative for relapsed/refractory (R/R) Hodgkin lymphoma (HL). Data on allo HCT outcomes in the era of new HL therapies are needed. We evaluated 72 R/R HL patients who received reduced intensity conditioning (RIC) allo HCT and compared the time periods 2009-2013 (n=20) to 2000-2008 (n=52). Grafts included HLA-matched sibling (35%), unrelated donor (8%) and umbilical cord blood (UCB, 56%). In recent period, patients more often received brentuximab vedotin (BV, 60% vs 2%), had fewer comorbidities (Sorror index 0: 60% vs 12%) and were in complete remission (50% vs 23%). Median follow-up was 4.4 years. Three-year progression-free survival (PFS) improved for patients treated between 2009-2013 (49%, 95% CI 26-68%) as compared to the earlier era (23%, 95% CI 13-35%, p=0.02). Overall survival (OS) at 3-years was 84% (95% CI 57-94%) vs 50% (95% CI 36-62%, p=0.01), reflecting lower non-relapse mortality and relapse rates. In multivariate analysis mortality was higher among those with chemoresistance (HR 3.83, 95% CI 1.38-10.57), while treatment during the recent era was associated with better OS (HR for period 2009-2013: 0.24, 95% CI 0.07-0.79) and PFS (HR 0.46, 95% CI 0.23-0.92). Allo HCT in patients with R/R HL is now a more effective treatment. |
format | Online Article Text |
id | pubmed-5415418 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
record_format | MEDLINE/PubMed |
spelling | pubmed-54154182017-07-30 Improving Outcomes After Allogeneic Hematopoietic Cell Transplantation for Hodgkin Lymphoma in the Brentuximab Vedotin Era Hegerova, Livia Cao, Qing Lazaryan, Aleksander McClune, Brian L. Weisdorf, Daniel J. Brunstein, Claudio G. Bachanova, Veronika Bone Marrow Transplant Article Allogeneic hematopoietic cell transplantation (allo HCT) remains a valuable alternative for relapsed/refractory (R/R) Hodgkin lymphoma (HL). Data on allo HCT outcomes in the era of new HL therapies are needed. We evaluated 72 R/R HL patients who received reduced intensity conditioning (RIC) allo HCT and compared the time periods 2009-2013 (n=20) to 2000-2008 (n=52). Grafts included HLA-matched sibling (35%), unrelated donor (8%) and umbilical cord blood (UCB, 56%). In recent period, patients more often received brentuximab vedotin (BV, 60% vs 2%), had fewer comorbidities (Sorror index 0: 60% vs 12%) and were in complete remission (50% vs 23%). Median follow-up was 4.4 years. Three-year progression-free survival (PFS) improved for patients treated between 2009-2013 (49%, 95% CI 26-68%) as compared to the earlier era (23%, 95% CI 13-35%, p=0.02). Overall survival (OS) at 3-years was 84% (95% CI 57-94%) vs 50% (95% CI 36-62%, p=0.01), reflecting lower non-relapse mortality and relapse rates. In multivariate analysis mortality was higher among those with chemoresistance (HR 3.83, 95% CI 1.38-10.57), while treatment during the recent era was associated with better OS (HR for period 2009-2013: 0.24, 95% CI 0.07-0.79) and PFS (HR 0.46, 95% CI 0.23-0.92). Allo HCT in patients with R/R HL is now a more effective treatment. 2017-01-30 2017-05 /pmc/articles/PMC5415418/ /pubmed/28134921 http://dx.doi.org/10.1038/bmt.2016.357 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Hegerova, Livia Cao, Qing Lazaryan, Aleksander McClune, Brian L. Weisdorf, Daniel J. Brunstein, Claudio G. Bachanova, Veronika Improving Outcomes After Allogeneic Hematopoietic Cell Transplantation for Hodgkin Lymphoma in the Brentuximab Vedotin Era |
title | Improving Outcomes After Allogeneic Hematopoietic Cell Transplantation for Hodgkin Lymphoma in the Brentuximab Vedotin Era |
title_full | Improving Outcomes After Allogeneic Hematopoietic Cell Transplantation for Hodgkin Lymphoma in the Brentuximab Vedotin Era |
title_fullStr | Improving Outcomes After Allogeneic Hematopoietic Cell Transplantation for Hodgkin Lymphoma in the Brentuximab Vedotin Era |
title_full_unstemmed | Improving Outcomes After Allogeneic Hematopoietic Cell Transplantation for Hodgkin Lymphoma in the Brentuximab Vedotin Era |
title_short | Improving Outcomes After Allogeneic Hematopoietic Cell Transplantation for Hodgkin Lymphoma in the Brentuximab Vedotin Era |
title_sort | improving outcomes after allogeneic hematopoietic cell transplantation for hodgkin lymphoma in the brentuximab vedotin era |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5415418/ https://www.ncbi.nlm.nih.gov/pubmed/28134921 http://dx.doi.org/10.1038/bmt.2016.357 |
work_keys_str_mv | AT hegerovalivia improvingoutcomesafterallogeneichematopoieticcelltransplantationforhodgkinlymphomainthebrentuximabvedotinera AT caoqing improvingoutcomesafterallogeneichematopoieticcelltransplantationforhodgkinlymphomainthebrentuximabvedotinera AT lazaryanaleksander improvingoutcomesafterallogeneichematopoieticcelltransplantationforhodgkinlymphomainthebrentuximabvedotinera AT mcclunebrianl improvingoutcomesafterallogeneichematopoieticcelltransplantationforhodgkinlymphomainthebrentuximabvedotinera AT weisdorfdanielj improvingoutcomesafterallogeneichematopoieticcelltransplantationforhodgkinlymphomainthebrentuximabvedotinera AT brunsteinclaudiog improvingoutcomesafterallogeneichematopoieticcelltransplantationforhodgkinlymphomainthebrentuximabvedotinera AT bachanovaveronika improvingoutcomesafterallogeneichematopoieticcelltransplantationforhodgkinlymphomainthebrentuximabvedotinera |