Radioimmunotherapy-augmented BEAM chemotherapy vs BEAM alone as the high-dose regimen for autologous stem cell transplantation (ASCT) in relapsed follicular lymphoma (FL): a retrospective study of the EBMT Lymphoma Working Party
Language English Country Great Britain, England Media print-electronic
Document type Comparative Study, Journal Article
PubMed
28530668
DOI
10.1038/bmt.2017.88
PII: bmt201788
Knihovny.cz E-resources
- MeSH
- Survival Analysis MeSH
- Transplantation, Autologous MeSH
- Cytarabine therapeutic use MeSH
- Adult MeSH
- Etoposide therapeutic use MeSH
- Lymphoma, Follicular mortality therapy MeSH
- Carmustine therapeutic use MeSH
- Combined Modality Therapy methods MeSH
- Middle Aged MeSH
- Humans MeSH
- Melphalan therapeutic use MeSH
- Young Adult MeSH
- Antineoplastic Combined Chemotherapy Protocols therapeutic use MeSH
- Radioimmunotherapy methods MeSH
- Retrospective Studies MeSH
- Rituximab therapeutic use MeSH
- Aged MeSH
- Case-Control Studies MeSH
- Hematopoietic Stem Cell Transplantation methods mortality MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Young Adult MeSH
- Male MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Comparative Study MeSH
- Names of Substances
- Cytarabine MeSH
- Etoposide MeSH
- Carmustine MeSH
- Melphalan MeSH
- Rituximab MeSH
Relapse remains the most common cause of treatment failure in patients receiving autologous stem cell transplantation (ASCT) for follicular lymphoma (FL). The aim of this study was to evaluate the effect of adding radioimmunotherapy or rituximab (R) to BEAM (carmustine, etoposide, ara-c, melphalan) high-dose therapy for ASCT in patients with relapsed FL. Using the European Society for Blood and Marrow Transplantation registry, we conducted a cohort comparison of BEAM (n=1973), Zevalin-BEAM (Z-BEAM) (n=207) and R-BEAM (n=179) and also a matched-cohort analysis of BEAM vs Z-BEAM including 282 and 154 patients, respectively. BEAM, Z-BEAM and R-BEAM groups were well balanced for age, time from diagnosis to ASCT and disease status at ASCT. The cumulative incidences of relapse (IR) at 2 years were 34, 34 and 32% for Z-BEAM, R-BEAM and BEAM, respectively. By multivariate analysis, there were no significant differences with Z-BEAM or R-BEAM compared with BEAM for IR, non-relapse mortality, event-free survival or overall survival. With the caveat that the limitations of registry analyses have to be taken into account, this study does not support adding radioimmunotherapy or R to BEAM in ASCT for relapsed FL. However, we cannot rule out the existence a particular subset of patients who could benefit from Z-BEAM conditioning that cannot be identified in our series, and this should be tested in a randomized trial.
Addenbrookes Hospital Cambridge UK
Azienda Ospedaliera Papa Giovanni XXIII Bergamo Italy
Bologna University S Orsola Malpighi Hospital Bologna Italy
Centre for Clinical Haematology Birmingham UK
Centre Henri Becquerel Rouen France
Centre Hospitalier Saint Louis Paris France
Centre Leon Berard Lyon France
Charles University Hospital Prague Czech Republic
CHU Lapeyronie Montpellier France
Cliniques Universitaires St Luc Brussels Belgium
Department of Haemato Oncology St Bartholomew's Hospital Barts Health NHS Trust London UK
Department of Medicine 5 University of Heidelberg Heidelberg Germany
Gartnaval General Hospital Glasgow UK
Hôpital Bretonneau Tours France
Hôpital Purpan Toulouse France
Hospices Civils de Lyon Pierre Benite France
Institut Paoli Calmettes Marseille France
Klinikum Chemnitz gGmbH Chemnitz Germany
Nottingham City Hospital Nottingham UK
Son Espases University Hospital Palma de Mallorca Spain
Southampton General Hospital Southampton UK
See more in PubMed
J Clin Oncol. 2009 Apr 1;27(10 ):1653-9 PubMed
J Clin Oncol. 2010 Aug 10;28(23):3709-16 PubMed
Ann Oncol. 2014 Nov;25(11):2224-9 PubMed
J Clin Oncol. 2013 May 1;31(13):1624-30 PubMed
J Clin Oncol. 2008 Nov 10;26(32):5175-82 PubMed
J Clin Oncol. 2013 May 1;31(13):1662-8 PubMed
J Clin Oncol. 2008 Jan 1;26(1):90-5 PubMed
J Clin Oncol. 2007 Sep 20;25(27):4285-92 PubMed
Leukemia. 2007 Nov;21(11):2324-31 PubMed
Ann Hematol. 2007 Feb;86(2):81-7 PubMed
J Clin Oncol. 2007 Jun 20;25(18):2554-9 PubMed
Blood. 2003 Oct 1;102(7):2351-7 PubMed
Ann Oncol. 2016 Sep;27(suppl 5):v83-v90 PubMed
Ann Oncol. 2013 Mar;24(3):561-76 PubMed
Oncologist. 2009;14 Suppl 2:41-51 PubMed
Blood. 2005 Oct 15;106(8):2896-902 PubMed
Haematologica. 2013 Jul;98(7):1014-21 PubMed
Cancer. 2012 Oct 1;118(19):4706-14 PubMed
Leuk Lymphoma. 2011 Jul;52(7):1188-99 PubMed
Exp Hematol. 2007 Apr;35(4):534-40 PubMed
Blood. 2005 Jun 15;105(12 ):4576-82 PubMed
Lancet. 2011 Jan 1;377(9759):42-51 PubMed
Clin Lymphoma Myeloma Leuk. 2011 Apr;11(2):212-8 PubMed