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      Bendamustine-based conditioning prior to autologous stem cell transplantation (ASCT): Results of a French multicenter study of 474 patients from LYmphoma Study Association (LYSA) centers

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          Autologous bone marrow transplantation as compared with salvage chemotherapy in relapses of chemotherapy-sensitive non-Hodgkin's lymphoma.

          High-dose chemotherapy followed by autologous bone marrow transplantation is a therapeutic option for patients with chemotherapy-sensitive non-Hodgkin's lymphoma who have relapses. In this report we describe a prospective randomized study of such treatment. A total of 215 patients with relapses of non-Hodgkin's lymphoma were treated between July 1987 and June 1994. All patients received two courses of conventional chemotherapy. The 109 patients who had a response to chemotherapy were randomly assigned to receive four courses of chemotherapy plus radiotherapy (54 patients) or radiotherapy plus intensive chemotherapy and autologous bone marrow transplantation (55 patients). The overall rate of response to conventional chemotherapy was 58 percent; among patients with relapses after chemotherapy, the response rate was 64 percent, and among those with relapses during chemotherapy, the response rate was 21 percent. There were three deaths from toxic effects among the patients in the transplantation group, and none among those in the group receiving chemotherapy without transplantation. The two groups did not differ in terms of prognostic factors. The median follow-up time was 63 months. The response rate was 84 percent after bone marrow transplantation and 44 percent after chemotherapy without transplantation. At five years, the rate of event-free survival was 46 percent in the transplantation group and 12 percent in the group receiving chemotherapy without transplantation (P = 0.001), and the rate of overall survival was 53 and 32 percent, respectively (P = 0.038). As compared with conventional chemotherapy, treatment with high-dose chemotherapy and autologous bone marrow transplantation increases event-free and overall survival in patients with chemotherapy-sensitive non-Hodgkin's lymphoma in relapse.
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            Hematopoietic SCT in Europe 2013: recent trends in the use of alternative donors showing more haploidentical donors but fewer cord blood transplants

            A record number of 39 209 HSCT in 34 809 patients (14 950 allogeneic (43%) and 19 859 autologous (57%)) were reported by 658 centers in 48 countries to the 2013 survey. Trends include: more growth in allogeneic than in autologous HSCT, increasing use of sibling and unrelated donors and a pronounced increase in haploidentical family donors when compared with cord blood donors for those patients without a matched related or unrelated donor. Main indications were leukemias, 11 190 (32% 96% allogeneic); lymphoid neoplasias, 19 958 (57% 11% allogeneic); solid tumors, 1543 (4% 4% allogeneic); and nonmalignant disorders, 1975 (6% 91% allogeneic). In patients without a matched sibling or unrelated donor, alternative donors are used. Since 2010 there has been a marked increase of 96% in the number of transplants performed from haploidentical relatives (802 in 2010 to 1571 in 2013), whereas the number of unrelated cord blood transplants has slightly decreased (789 in 2010 to 666 in 2013). The use of donor type varies greatly throughout Europe.
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              Impact of Conditioning Regimen on Outcomes for Patients with Lymphoma Undergoing High-Dose Therapy with Autologous Hematopoietic Cell Transplantation

              There are limited data to guide the choice of high-dose therapy (HDT) regimen before autologous hematopoietic cell transplantation (AHCT) for patients with Hodgkin (HL) and non-Hodgkin lymphoma (NHL). We studied 4917 patients (NHL, n = 3905; HL, n = 1012) who underwent AHCT from 1995 to 2008 using the most common HDT platforms: carmustine (BCNU), etoposide, cytarabine, and melphalan (BEAM) (n = 1730); cyclophosphamide, BCNU, and etoposide (CBV) (n = 1853); busulfan and cyclophosphamide (BuCy) (n = 789); and total body irradiation (TBI)-containing treatment (n = 545). CBV was divided into CBV(high) and CBV(low) based on BCNU dose. We analyzed the impact of regimen on development of idiopathic pulmonary syndrome (IPS), transplantation-related mortality (TRM), and progression-free and overall survival. The 1-year incidence of IPS was 3% to 6% and was highest in recipients of CBV(high) (hazard ratio [HR], 1.9) and TBI (HR, 2.0) compared with BEAM. One-year TRM was 4% to 8%, respectively, and was similar between regimens. Among patients with NHL, there was a significant interaction between histology, HDT regimen, and outcome. Compared with BEAM, CBV(low) (HR, .63) was associated with lower mortality in follicular lymphoma (P < .001), and CBV(high) (HR, 1.44) was associated with higher mortality in diffuse large B cell lymphoma (P = .001). For patients with HL, CBV(high) (HR, 1.54), CBV(low) (HR, 1.53), BuCy (HR, 1.77), and TBI (HR, 3.39) were associated with higher mortality compared with BEAM (P < .001). The impact of specific AHCT regimen on post-transplantation survival is different depending on histology; therefore, further studies are required to define the best regimen for specific diseases.
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                Author and article information

                Journal
                American Journal of Hematology
                Am J Hematol
                Wiley
                03618609
                June 2018
                June 2018
                March 14 2018
                : 93
                : 6
                : 729-735
                Affiliations
                [1 ]Institut d'Hématologie de Basse-Normandie, CHU; Caen France
                [2 ]Department of Hematology; Institut Paoli Calmettes; Marseille
                [3 ]Department of Clinical Hematology; University Hospital Montpellier; Montpellier France
                [4 ]Hematology Department; Centre Antoine Lacassagne; Nice France
                [5 ]Hematology, Toulouse University Hospital; Toulouse France
                [6 ]Clinical Research Department; Amiens University hospital; Amiens EA4666 France
                [7 ]Haematology, University Hospital; Strasbourg France
                [8 ]Hematology, University hospital; Rennes France
                [9 ]Department of Hematology; Nantes University Hospital; Nantes France
                [10 ]Department of Hematology; Curie Institute, Hôpital René Huguenin; Saint-Cloud France
                [11 ]Service d'hématologie clinique adulte et de thérapie cellulaire, CHU ESTAING, EA 7453 CHELTER, Université Clermont Auvergne CIC-501; Clermont-Ferrand France
                [12 ]Oncopole Hopital Sud; Amiens FRA
                [13 ]Makassed General Hospital; Beirut LBN
                [14 ]Institut d'Hématologie de Basse-Normandie, Centre François Baclesse; Caen France
                [15 ]Hematology and Cell Therapy; Etablissement Hospitalier Universitaire (EHU) 1st November; Oran Algeria
                [16 ]Hematology, University Hospital; Dijon France
                [17 ]Hematology, CHU Grenoble; Grenoble France
                [18 ]Oncologie hématologique et thérapie cellulaire, CHU Poitiers; Poitiers France
                [19 ]Hematology, Hôpital HURIEZ UAM allogreffe de CSH, CHRU; Lille France
                [20 ]Haematology, CHU de Bordeaux; Bordeaux France
                [21 ]Department of Hematology; Centre Hospitalier Universitaire; Reims Cedex FRA
                [22 ]Microenvironnement Cellulaire et Pathologies, Normandie Univ, Unicaen; MILPAT Caen 14000 France
                Article
                10.1002/ajh.25077
                29473209
                18dd6f87-c363-4757-838f-e12a7f904d6f
                © 2018

                http://doi.wiley.com/10.1002/tdm_license_1.1

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