9
views
0
recommends
+1 Recommend
2 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Hematopoietic cell transplantation and cellular therapies in Europe 2021. The second year of the SARS-CoV-2 pandemic. A Report from the EBMT Activity Survey

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          In 2021, 47,412 HCT (19,806 (42%) allogeneic and 27,606 (58%) autologous) in 43,109 patients were reported by 694 European centers. 3494 patients received advanced cellular therapies, 2524 of which were CAR-T treatments, an additional 3245 received DLI. Changes compared to the previous year were CAR-T treatment (+35%), allogeneic HCT +5.4%, autologous HCT +3.9%, more pronounced in non-malignant disorders. Main indications for allogeneic HCT were myeloid malignancies 10,745 (58%), lymphoid malignancies 5127 (28%) and non-malignant disorders 2501 (13%). Main indications for autologous HCT were lymphoid malignancies 22,129 (90%) and solid tumors 1635 (7%). In allogeneic HCT, use of haploidentical donors decreased by −0.9% while use of unrelated and sibling donors increased by +4.3% and +9%. Cord blood HCT decreased by −5.8%. Pediatric HCT increased overall by +5.6% (+6.9% allogeneic and +1.6% autologous). Increase in the use of CAR-T was mainly restricted to high-income countries. The drop in HCT activity reported in 2020 partially recovered in 2021, the second year of the SARS-CoV-2 pandemic. The transplant community confronted with the pandemic challenge, continued in providing patients access to treatment. This annual EBMT report reflects current activities useful for health care resource planning.

          Related collections

          Most cited references35

          • Record: found
          • Abstract: found
          • Article: not found

          Tisagenlecleucel in Adult Relapsed or Refractory Diffuse Large B-Cell Lymphoma

          Patients with diffuse large B-cell lymphoma that is refractory to primary and second-line therapies or that has relapsed after stem-cell transplantation have a poor prognosis. The chimeric antigen receptor (CAR) T-cell therapy tisagenlecleucel targets and eliminates CD19-expressing B cells and showed efficacy against B-cell lymphomas in a single-center, phase 2a study.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Chimeric antigen receptor T cells for sustained remissions in leukemia.

            Relapsed acute lymphoblastic leukemia (ALL) is difficult to treat despite the availability of aggressive therapies. Chimeric antigen receptor-modified T cells targeting CD19 may overcome many limitations of conventional therapies and induce remission in patients with refractory disease. We infused autologous T cells transduced with a CD19-directed chimeric antigen receptor (CTL019) lentiviral vector in patients with relapsed or refractory ALL at doses of 0.76×10(6) to 20.6×10(6) CTL019 cells per kilogram of body weight. Patients were monitored for a response, toxic effects, and the expansion and persistence of circulating CTL019 T cells. A total of 30 children and adults received CTL019. Complete remission was achieved in 27 patients (90%), including 2 patients with blinatumomab-refractory disease and 15 who had undergone stem-cell transplantation. CTL019 cells proliferated in vivo and were detectable in the blood, bone marrow, and cerebrospinal fluid of patients who had a response. Sustained remission was achieved with a 6-month event-free survival rate of 67% (95% confidence interval [CI], 51 to 88) and an overall survival rate of 78% (95% CI, 65 to 95). At 6 months, the probability that a patient would have persistence of CTL019 was 68% (95% CI, 50 to 92) and the probability that a patient would have relapse-free B-cell aplasia was 73% (95% CI, 57 to 94). All the patients had the cytokine-release syndrome. Severe cytokine-release syndrome, which developed in 27% of the patients, was associated with a higher disease burden before infusion and was effectively treated with the anti-interleukin-6 receptor antibody tocilizumab. Chimeric antigen receptor-modified T-cell therapy against CD19 was effective in treating relapsed and refractory ALL. CTL019 was associated with a high remission rate, even among patients for whom stem-cell transplantation had failed, and durable remissions up to 24 months were observed. (Funded by Novartis and others; CART19 ClinicalTrials.gov numbers, NCT01626495 and NCT01029366.).
              Bookmark
              • Record: found
              • Abstract: not found
              • Article: not found

              Chimeric Antigen Receptor Therapy.

                Bookmark

                Author and article information

                Contributors
                jakob.passweg@usb.ch
                Journal
                Bone Marrow Transplant
                Bone Marrow Transplant
                Bone Marrow Transplantation
                Nature Publishing Group UK (London )
                0268-3369
                1476-5365
                6 March 2023
                6 March 2023
                : 1-12
                Affiliations
                [1 ]GRID grid.410567.1, EBMT Activity Survey Office, Hematology Division, , University Hospital, ; Basel, Switzerland
                [2 ]GRID grid.15496.3f, ISNI 0000 0001 0439 0892, Unit of Hematology and Bone Marrow Transplantation, IRCCS San Raffaele Scientific Institute, , Vita-Salute San Raffaele University, ; Milan, Italy
                [3 ]GRID grid.7727.5, ISNI 0000 0001 2190 5763, Department of Pediatric Hematology, Oncology and Stem Cell Transplantation, , University of Regensburg, ; Regensburg, Germany
                [4 ]GRID grid.411251.2, ISNI 0000 0004 1767 647X, Hematology Department, , Hospital Universitario de la Princesa, ; Madrid, Spain
                [5 ]GRID grid.10417.33, ISNI 0000 0004 0444 9382, Laboratory of Hematology, Department of Laboratory Medicine, , Radboud University Medical Center, ; Nijmegen, The Netherlands
                [6 ]GRID grid.491869.b, ISNI 0000 0000 8778 9382, Klinik für Hämatologie und Stammzelltransplantation, , HELIOS Klinikum Berlin-Buch, ; Berlin, Germany
                [7 ]GRID grid.52996.31, ISNI 0000 0000 8937 2257, Department of Haematology, , University College London Hospitals NHS Foundation Trust, ; London, UK
                [8 ]GRID grid.50550.35, ISNI 0000 0001 2175 4109, Pediatric Immune-hematology Unit, Necker Children Hospital, , Assistance Publique Hôpitaux de Paris, ; Paris, France
                [9 ]BMT Unit, Department of Hematology, Hospital St. Louis, Paris, France
                [10 ]GRID grid.412688.1, ISNI 0000 0004 0397 9648, School of Medicine, University of Zagreb, , University Hospital Center Zagreb, ; Zagreb, Croatia
                [11 ]GRID grid.31410.37, ISNI 0000 0000 9422 8284, Department of Haematology, , Sheffield Teaching Hospitals NHS Foundation Trust, ; Sheffield, UK
                [12 ]GRID grid.5841.8, ISNI 0000 0004 1937 0247, Clinical Hematology Department, Institut Català d’Oncologia-Hospitalet, Institut d’Investigació Biomèdica de Bellvitge (IDIBELL), , University of Barcelona, ; Barcelona, Spain
                Author information
                http://orcid.org/0000-0002-6554-483X
                http://orcid.org/0000-0002-8189-5779
                http://orcid.org/0000-0002-6117-5328
                http://orcid.org/0000-0003-1224-091X
                http://orcid.org/0000-0001-9458-8025
                http://orcid.org/0000-0001-6819-3476
                Article
                1943
                10.1038/s41409-023-01943-3
                9987384
                36879108
                72efd5fc-505d-43a4-8abf-08a53b9dbb0b
                © The Author(s) 2023

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 26 January 2023
                : 6 February 2023
                : 16 February 2023
                Categories
                Article

                Transplantation
                haematological cancer,leukaemia
                Transplantation
                haematological cancer, leukaemia

                Comments

                Comment on this article