LEAM vs. BEAM vs. CLV Conditioning Regimen for Autologous Stem Cell Transplantation in Malignant Lymphomas. Retrospective Comparison of Toxicity and Efficacy on 222 Patients in the First 100 Days After Transplant, On Behalf of the Romanian Society for Bone Marrow Transplantation.
autologous stem cell transplantation
conditioning chemotherapy
real-life data
relapsed/refractory lymphoma
retrospective analysis
Journal
Frontiers in oncology
ISSN: 2234-943X
Titre abrégé: Front Oncol
Pays: Switzerland
ID NLM: 101568867
Informations de publication
Date de publication:
2019
2019
Historique:
received:
26
05
2019
accepted:
27
08
2019
entrez:
26
9
2019
pubmed:
26
9
2019
medline:
26
9
2019
Statut:
epublish
Résumé
High-dose chemotherapy (HDT) followed by autologous hematopoietic stem cell transplantation (ASCT) is widely used in patients with malignant lymphomas. In Europe over 8,000 ASCTs for lymphoma were performed out of a total of 40,000 transplants according to the European Bone Marrow Transplant (EBMT) activity survey in 2017. ASCT is considered the standard treatment for eligible patients failing to achieve remission after first line chemotherapy or patients with relapsed or refractory lymphomas, including classical Hodkin's lymphoma, diffuse large B-cell lymphoma, mantle cell lymphoma, and follicular lymphoma, as well as consolidation therapy in first remission in mantle cell lymphoma. BEAM (BCNU/carmustine, etoposide, cytarabine, and melphalan) is the most commonly used conditioning regimen for ASCT in patients with relapsed/refractory (R/R) lymphomas in Europe, whereas the CBV (cyclophosphamide, BCNU, and etoposide) regimen is also widely used in North America. Recently, concerns regarding BCNU toxicity as well as restricted availability of BCNU and melphalan has determined an increasing number of transplant centers to use alternative conditioning regimens. Currently, only a few comparative studies, most of them retrospective, between different conditioning protocols regarding efficacy and toxicity have been published. Thus, in the current manuscript, we report the experience of 2 transplant centers in ASCT in R/R lymphomas with three types of conditioning: BEAM, CLV (cyclophosphamide, lomustine, etoposide) and LEAM (lomustine, etoposide, cytarabine, and melphalan), with the aim to evaluate the results of alternative conditioning regimens using lomustine (LEAM and CLV) and compare them with the standard BEAM regarding early toxicity, engraftment, and transplant related mortality (TRM). All patients developed grade IV neutropenia, anemia with/without transfusion necessity. Severe thrombocytopenia with transfusion requirements is reported in most cases. Median time to platelet engraftment and neutrophil engraftment was 13 days (range) and 10 days (range), respectively. Gastrointestinal toxicity was the most common non-hematologic toxicity after all three conditioning regimens. Oral mucositis in various grades from I to IV was diagnosed in most cases. Other side effects include vomiting, diarrhea, colitis, and skin rash but with low severity grades. For the LEAM arm, one patient died after transplant, before engrafting, one patient didn't achieve platelet engraftment in day 100, one patient developed grade 3 upper gastrointestinal bleeding, one patient died (grade 5 toxicity) with acute renal failure, one patient developed hypoxic events up to grade 4 acute respiratory failure and one patient developed grade 3 itchy skin rash. For the CLV arm, one patient died after transplant, before engrafting, one patient developed grade 3 colitis, one patient with grade 3 hepatic cytolysis, one patient with cardiac toxicity followed by death (grade 5) caused by an acute myocardial infarction with ST elevation and one patient with pulmonary toxicity clinically manifested with grade 3 pleurisy. For the BEAM arm, one patient developed grade 3 cardiac toxicity with sinus bradycardia and afterwards grade 4 with acute pulmonary edema, three patients presented a grade 3 pruritic skin rash and two patients developed grade 3 seizures. In the present study we presented the differences that were observed between BEAM, LEAM, and CLV conditioning regimens offering clinical arguments for an SCT practitioner choice in the ideal situation, but also of choice for alternative regimens in the case that one regimen cannot be used.
Identifiants
pubmed: 31552193
doi: 10.3389/fonc.2019.00892
pmc: PMC6746965
doi:
Types de publication
Journal Article
Langues
eng
Pagination
892Références
Blood. 2001 Feb 1;97(3):616-23
pubmed: 11157476
Biol Blood Marrow Transplant. 2001;7(10):552-60
pubmed: 11760087
N Engl J Med. 2002 Jan 24;346(4):235-42
pubmed: 11807147
J Clin Oncol. 2003 Jun 15;21(12):2320-5
pubmed: 12805333
Bone Marrow Transplant. 2004 Oct;34(7):581-7
pubmed: 15273714
Haematologica. 1991 Mar;76 Suppl 1:66-71
pubmed: 1713875
Haematologica. 2007 Jan;92(1):35-41
pubmed: 17229633
J Clin Oncol. 1991 Oct;9(10):1871-9
pubmed: 1919637
Hematol Oncol. 2011 Jun;29(2):75-80
pubmed: 20635327
Blood. 2010 Dec 2;116(23):4934-7
pubmed: 20733154
Exp Clin Transplant. 2012 Apr;10(2):163-7
pubmed: 22432762
Rom J Morphol Embryol. 2012;53(2):343-50
pubmed: 22732804
Cochrane Database Syst Rev. 2013 Jun 20;(6):CD009411
pubmed: 23784872
Leuk Lymphoma. 2014 Jul;55(7):1657-60
pubmed: 24024474
Crit Rev Oncol Hematol. 2014 Oct;92(1):1-10
pubmed: 24855908
Bone Marrow Transplant. 2014 Sep;49(9):1239-40
pubmed: 24887380
Springerplus. 2013 Sep 26;2:489
pubmed: 25674395
Biol Blood Marrow Transplant. 2015 Jun;21(6):1046-1053
pubmed: 25687795
Biol Blood Marrow Transplant. 2016 Mar;22(3):493-8
pubmed: 26497906
Int J Hematol. 2016 Mar;103(3):292-8
pubmed: 26729297
Bone Marrow Transplant. 2016 Jun;51(6):786-92
pubmed: 26901709
Acta Haematol. 2016;135(4):211-6
pubmed: 26914538
Curr Treat Options Oncol. 2016 May;17(5):24
pubmed: 27032646
Bone Marrow Transplant. 2016 Oct;51(10):1397-1399
pubmed: 27214072
Cancer. 2016 Nov 15;122(21):3316-3326
pubmed: 27404668
Semin Hematol. 2016 Jul;53(3):180-5
pubmed: 27496309
Rom J Intern Med. 2016 Sep 1;54(3):194-200
pubmed: 27658169
Cancer Med. 2016 Nov;5(11):3059-3067
pubmed: 27699999
Oncotarget. 2017 Dec 15;9(1):1483-1491
pubmed: 29416707
Front Immunol. 2018 Feb 19;9:239
pubmed: 29515572
Crit Rev Clin Lab Sci. 2018 Aug;55(5):329-345
pubmed: 29801428
Bone Marrow Transplant. 2019 Apr;54(4):625-628
pubmed: 30283147
CA Cancer J Clin. 2019 Jan;69(1):7-34
pubmed: 30620402
J Clin Med. 2019 Jun 20;8(6):null
pubmed: 31226876
J Clin Med. 2019 Aug 06;8(8):null
pubmed: 31390838
Cancer. 1983 May 15;51(10):1814-8
pubmed: 6572542
Cancer. 1995 Mar 15;75(6):1354-9
pubmed: 7882286
Bone Marrow Transplant. 1997 Sep;20(6):451-8
pubmed: 9313877