Literature DB >> 22544699

Prospective study of rabbit antithymocyte globulin and cyclosporine for aplastic anemia from the EBMT Severe Aplastic Anaemia Working Party.

Judith C Marsh1, Andrea Bacigalupo, Hubert Schrezenmeier, Andre Tichelli, Antonio M Risitano, Jakob R Passweg, Sally B Killick, Alan J Warren, Theodora Foukaneli, Mahmoud Aljurf, H A Al-Zahrani, Britta Höchsmann, Philip Schafhausen, Alexander Roth, Anke Franzke, Tim H Brummendorf, Carlo Dufour, Rosi Oneto, Philip Sedgwick, Alain Barrois, Shahram Kordasti, Modupe O Elebute, Ghulam J Mufti, Gerard Socie.   

Abstract

Rabbit antithymocyte globulin (rATG; thymoglobulin, Genzyme) in combination with cyclosporine, as first-line immunosuppressive therapy, was evaluated prospectively in a multicenter, European, phase 2 pilot study, in 35 patients with aplastic anemia. Results were compared with 105 age- and disease severity-matched patients from the European Blood and Marrow Transplant registry, treated with horse ATG (hATG; lymphoglobulin) and cyclosporine. The primary end point was response at 6 months. At 3 months, no patients had achieved a complete response to rATG. Partial response occurred in 11 (34%). At 6 months, complete response rate was 3% and partial response rate 37%. There were 10 deaths after rATG (28.5%) and 1 after subsequent HSCT. Infections were the main cause of death in 9 of 10 patients. The best response rate was 60% for rATG and 67% for hATG. For rATG, overall survival at 2 years was 68%, compared with 86% for hATG (P = .009). Transplant-free survival was 52% for rATG and 76% for hATG (P = .002). On multivariate analysis, rATG (hazard ratio = 3.9, P = .003) and age more than 37 years (hazard ratio = 4.7, P = .0008) were independent adverse risk factors for survival. This study was registered at www.clinicaltrials.gov as NCT00471848.

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Year:  2012        PMID: 22544699     DOI: 10.1182/blood-2012-02-407684

Source DB:  PubMed          Journal:  Blood        ISSN: 0006-4971            Impact factor:   22.113


  52 in total

1.  Effectiveness and safety of rabbit anti-thymocyte globulin in Japanese patients with aplastic anemia.

Authors:  Tatsuhiro Sakamoto; Naoshi Obara; Naoki Kurita; Mamiko Sakata-Yanagimoto; Hidekazu Nishikii; Yasuhisa Yokoyama; Kazumi Suzukawa; Yuichi Hasegawa; Shigeru Chiba
Journal:  Int J Hematol       Date:  2013-08-21       Impact factor: 2.490

2.  Optimizing conditioning regimen with low-dose irradiation or busulfan enables the outcome of transplantation from a 6-7/8 HLA-matched donor comparable to that from an 8/8 HLA-matched unrelated donor in severe aplastic anemia patients under 40 years.

Authors:  Xia Qin; Yi-Ping Zhu; Cheng-Juan Luo; Ming Zhou; Ke Huang; Chun Chen; Wei-Ping Zhang; Yuan Sun; Rong-Mu Luo; Xiang-Feng Tang; Ting Yang; Xian-Min Song; Shao-Yan Hu; Zi-Min Sun; Jiong Hu; Shun-Qing Wang; Jing Chen
Journal:  Ann Hematol       Date:  2021-05-14       Impact factor: 3.673

3.  Repeat course of rabbit antithymocyte globulin as salvage following initial therapy with rabbit antithymocyte globulin in acquired aplastic anemia.

Authors:  Diego V Clé; Elias H Atta; Danielle S P Dias; Carlos B L Lima; Mariana Bonduel; Gabriela Sciuccati; Larissa A Medeiros; Michel M de Oliveira; Marco A Salvino; Marlene Garanito; Sara T Ollala Saad; Rodrigo T Calado; Phillip Scheinberg
Journal:  Haematologica       Date:  2015-04-10       Impact factor: 9.941

4.  Clinical and morphological predictors of outcome in older aplastic anemia patients treated with eltrombopag.

Authors:  Bruno Fattizzo; Austin G Kulasekararaj; Anita Hill; Nana Benson-Quarm; Morag Griffin; Talha Munir; Louise Arnold; Kathryn Riley; Robin Ireland; Hugues De Lavallade; Victoria Potter; Dario Consonni; Peter Hillmen; Ghulam J Mufti; Wilma Barcellini; Judith C W Marsh
Journal:  Haematologica       Date:  2019-03-19       Impact factor: 9.941

Review 5.  Activity of eltrombopag in severe aplastic anemia.

Authors:  Phillip Scheinberg
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2018-11-30

Review 6.  Activity of eltrombopag in severe aplastic anemia.

Authors:  Phillip Scheinberg
Journal:  Blood Adv       Date:  2018-11-13

7.  Immunosuppressive therapy versus alternative donor hematopoietic stem cell transplantation for children with severe aplastic anemia who lack an HLA-matched familial donor.

Authors:  Y B Choi; E S Yi; J W Lee; K W Sung; H H Koo; K H Yoo
Journal:  Bone Marrow Transplant       Date:  2016-09-26       Impact factor: 5.483

8.  Treg sensitivity to FasL and relative IL-2 deprivation drive idiopathic aplastic anemia immune dysfunction.

Authors:  Shok Ping Lim; Benedetta Costantini; Syed A Mian; Pilar Perez Abellan; Shreyans Gandhi; Marc Martinez Llordella; Juan Jose Lozano; Rita Antunes Dos Reis; Giovanni A M Povoleri; Thanos P Mourikis; Ander Abarrategi; Linda Ariza-McNaughton; Susanne Heck; Jonathan M Irish; Giovanna Lombardi; Judith C W Marsh; Dominique Bonnet; Shahram Kordasti; Ghulam J Mufti
Journal:  Blood       Date:  2020-08-13       Impact factor: 22.113

9.  Long-term outcome after immunosuppressive therapy with horse or rabbit antithymocyte globulin and cyclosporine for severe aplastic anemia in children.

Authors:  Dae Chul Jeong; Nack Gyun Chung; Bin Cho; Yao Zou; Min Ruan; Yoshiyuki Takahashi; Hideki Muramatsu; Akira Ohara; Yoshiyuki Kosaka; Wenyu Yang; Hack Ki Kim; Xiaofan Zhu; Seiji Kojima
Journal:  Haematologica       Date:  2013-11-08       Impact factor: 9.941

10.  Clinical outcomes in adult patients with aplastic anemia: A single institution experience.

Authors:  Prajwal Boddu; Guillermo Garcia-Manero; Farhad Ravandi; Gautam Borthakur; Elias Jabbour; Courtney DiNardo; Nitin Jain; Naval Daver; Naveen Pemmaraju; Paolo Anderlini; Simrit Parmar; Devendra Kc; Mary Akosile; Sherry A Pierce; Richard Champlin; Jorge Cortes; Hagop Kantarjian; Tapan Kadia
Journal:  Am J Hematol       Date:  2017-09-25       Impact factor: 10.047

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