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
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

892

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Auteurs

Andrei Colita (A)

Department of Hematology, Carol Davila University of Medicine and Pharmacy, Bucharest, Romania.
Department of Stem Cell Transplantation, Coltea Clinical Hospital, Bucharest, Romania.

Anca Colita (A)

Department of Pediatrics, Carol Davila University of Medicine and Pharmacy, Bucharest, Romania.
Department of Stem Cell Transplantation, Fundeni Clinical Institute, Bucharest, Romania.

Horia Bumbea (H)

Department of Hematology, Carol Davila University of Medicine and Pharmacy, Bucharest, Romania.
Department of Stem Cell Transplantation, University Hospital, Bucharest, Romania.

Adina Croitoru (A)

Department of Stem Cell Transplantation, Fundeni Clinical Institute, Bucharest, Romania.

Carmen Orban (C)

Department of Stem Cell Transplantation, Fundeni Clinical Institute, Bucharest, Romania.

Lavinia Eugenia Lipan (LE)

Department of Stem Cell Transplantation, Fundeni Clinical Institute, Bucharest, Romania.

Oana-Gabriela Craciun (OG)

Department of Stem Cell Transplantation, Fundeni Clinical Institute, Bucharest, Romania.

Dan Soare (D)

Department of Hematology, Carol Davila University of Medicine and Pharmacy, Bucharest, Romania.
Department of Stem Cell Transplantation, University Hospital, Bucharest, Romania.

Cecilia Ghimici (C)

Department of Hematology, Carol Davila University of Medicine and Pharmacy, Bucharest, Romania.
Department of Stem Cell Transplantation, Coltea Clinical Hospital, Bucharest, Romania.

Raluca Manolache (R)

Department of Hematology, Carol Davila University of Medicine and Pharmacy, Bucharest, Romania.
Department of Stem Cell Transplantation, Coltea Clinical Hospital, Bucharest, Romania.

Ionel Gelatu (I)

Department of Hematology, Carol Davila University of Medicine and Pharmacy, Bucharest, Romania.
Department of Stem Cell Transplantation, Coltea Clinical Hospital, Bucharest, Romania.

Ana-Maria Vladareanu (AM)

Department of Hematology, Carol Davila University of Medicine and Pharmacy, Bucharest, Romania.

Sergiu Pasca (S)

Department of Hematology, Research Center for Functional Genomics and Translational Medicine, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj Napoca, Romania.
Department of Hematology, Ion Chiricuta Clinical Cancer Center, Cluj Napoca, Romania.

Patric Teodorescu (P)

Department of Hematology, Ion Chiricuta Clinical Cancer Center, Cluj Napoca, Romania.
Department of Hematology, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj Napoca, Romania.

Delia Dima (D)

Department of Hematology, Ion Chiricuta Clinical Cancer Center, Cluj Napoca, Romania.

Anca Lupu (A)

Department of Hematology, Carol Davila University of Medicine and Pharmacy, Bucharest, Romania.
Department of Stem Cell Transplantation, Coltea Clinical Hospital, Bucharest, Romania.

Daniel Coriu (D)

Department of Hematology, Carol Davila University of Medicine and Pharmacy, Bucharest, Romania.
Department of Hematology, Fundeni Clinical Institute, Bucharest, Romania.

Ciprian Tomuleasa (C)

Department of Hematology, Research Center for Functional Genomics and Translational Medicine, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj Napoca, Romania.
Department of Hematology, Ion Chiricuta Clinical Cancer Center, Cluj Napoca, Romania.

Alina Tanase (A)

Department of Stem Cell Transplantation, Fundeni Clinical Institute, Bucharest, Romania.

Classifications MeSH