临床治疗新探索:全反式维甲酸联合小剂量CD20单克隆抗体治疗成人免疫性血小板减少症

张晓辉. 临床治疗新探索:全反式维甲酸联合小剂量CD20单克隆抗体治疗成人免疫性血小板减少症[J]. 临床血液学杂志, 2024, 37(1): 6-9. doi: 10.13201/j.issn.1004-2806.2024.01.002
引用本文: 张晓辉. 临床治疗新探索:全反式维甲酸联合小剂量CD20单克隆抗体治疗成人免疫性血小板减少症[J]. 临床血液学杂志, 2024, 37(1): 6-9. doi: 10.13201/j.issn.1004-2806.2024.01.002
ZHANG Xiaohui. New exploration in clinical treatment: All-trans retinoic acid plus low-dose rituximab in the treatment of adult immune thrombocytopenia[J]. J Clin Hematol, 2024, 37(1): 6-9. doi: 10.13201/j.issn.1004-2806.2024.01.002
Citation: ZHANG Xiaohui. New exploration in clinical treatment: All-trans retinoic acid plus low-dose rituximab in the treatment of adult immune thrombocytopenia[J]. J Clin Hematol, 2024, 37(1): 6-9. doi: 10.13201/j.issn.1004-2806.2024.01.002

临床治疗新探索:全反式维甲酸联合小剂量CD20单克隆抗体治疗成人免疫性血小板减少症

详细信息
    作者简介:

    专家简介:张晓辉,主任医师,二级教授,博士/后导师。现任北京大学人民医院血液科、北京大学血液病研究所副所长,国家血液系统疾病临床医学研究中心副主任兼办公室主任,中华医学会血液学分会委员会副主任委员、造血干细胞应用学组组长,中国免疫学会血液免疫分会委员会副主任委员,北京癌症防治学会血液工作委员会主任委员兼理事长。作为课题负责人主持国家科技重大专项、国家自然科学基金重点项目、首都卫生发展科研重点项目等;牵头/执笔中国专家指南/共识28部,主编血液领域专著5部,国家发明专利申请/授权14项,以第一/通讯作者发表SCI论文122篇,包括Nat ImmunolJ Hematol OncolLancet HaematolBloodNat CommunAm J HematolLeukemia等。荣获“国之名医·卓越建树”称号;以第一完成人荣获华夏医学科技奖一等奖、中华医学科技奖二等奖;以共同完成人荣获国家科技进步二等奖(2项)

    通讯作者: 张晓辉,E-mail:zhangxh100@sina.com
  • 中图分类号: R558.2

New exploration in clinical treatment: All-trans retinoic acid plus low-dose rituximab in the treatment of adult immune thrombocytopenia

More Information
  • 免疫性血小板减少症是一种孤立的血小板减少症,其特点是免疫失耐受介导的血小板破坏增多和血小板生成减少。其治疗包括皮质类固醇、静脉注射免疫球蛋白、利妥昔单抗、血小板生成素受体激动剂、免疫抑制剂和脾切除术。尽管目前的疗法对2/3以上的患者有效,但仍有一些患者无法获得长期疗效。本文介绍了全反式维甲酸联合小剂量CD20单克隆抗体治疗成人免疫性血小板减少症的疗效、安全性以及应用前景。
  • 加载中
  • [1]

    Cooper N, Ghanima W. Immune Thrombocytopenia[J]. N Engl J Med, 2019, 381(10): 945-955. doi: 10.1056/NEJMcp1810479

    [2]

    McMillan R, Wang L, Tomer A, et al. Suppression of in vitro megakaryocyte production by antiplatelet autoantibodies from adult patients with chronic ITP[J]. Blood, 2004, 103(4): 1364-1369. doi: 10.1182/blood-2003-08-2672

    [3]

    Olsson B, Andersson PO, Jernas M, et al. T-cell-mediated cytotoxicity toward platelets in chronic idiopathic thrombocytopenic purpura[J]. Nat Med, 2003, 9(9): 1123-1124. doi: 10.1038/nm921

    [4]

    Berchtold P, Wenger M. Autoantibodies against platelet glycoproteins in autoimmune thrombocytopenic purpura: their clinical significance and response to treatment[J]. Blood, 1993, 81(5): 1246-1250. doi: 10.1182/blood.V81.5.1246.1246

    [5]

    Terrell DR, Beebe LA, Vesely SK, et al. The incidence of immune thrombocytopenic purpura in children and adults: A critical review of published reports[J]. Am J Hematol, 2010, 85(3): 174-180. doi: 10.1002/ajh.21616

    [6]

    Moulis G, Palmaro A, Montastruc JL, et al. Epidemiology of incident immune thrombocytopenia: a nationwide population-based study in France[J]. Blood, 2014, 124(22): 3308-3315. doi: 10.1182/blood-2014-05-578336

    [7]

    Neunert C, Terrell DR, Arnold DM, et al. American Society of Hematology 2019 guidelines for immune thrombocytopenia[J]. Blood Adv, 2019, 3(23): 3829-3866. doi: 10.1182/bloodadvances.2019000966

    [8]

    Provan D, Arnold DM, Bussel JB, et al. Updated international consensus report on the investigation and management of primary immune thrombocytopenia[J]. Blood Adv, 2019, 3(22): 3780-3817. doi: 10.1182/bloodadvances.2019000812

    [9]

    Depré F, Aboud N, Mayer B, et al. Efficacy and tolerability of old and new drugs used in the treatment of immune thrombocytopenia: Results from a long-term observation in clinical practice[J]. PLoS One, 2018, 13(6): e0198184. doi: 10.1371/journal.pone.0198184

    [10]

    Imbach P, Barandun S, d'Apuzzo V, et al. High-dose intravenous gammaglobulin for idiopathic thrombocytopenic purpura in childhood[J]. Lancet, 1981, 317(8232): 1228-1231. doi: 10.1016/S0140-6736(81)92400-4

    [11]

    Schwab I, Nimmerjahn F. Intravenous immunoglobulin therapy: how does IgG modulate the immune system?[J]. Nat Rev Immunol, 2013, 13(3): 176-189. doi: 10.1038/nri3401

    [12]

    Cines DB, Blanchette VS. Immune Thrombocytopenic Purpura[J]. N Engl J Med, 2002, 346(13): 995-1008. doi: 10.1056/NEJMra010501

    [13]

    Huang ME, Ye YC, Chen SR, et al. Use of all-trans retinoic acid in the treatment of acute promyelocytic leukemia[J]. Blood, 1988, 72(2): 567-572. doi: 10.1182/blood.V72.2.567.567

    [14]

    Breitman TR, Collins SJ, Keene BR. Terminal differentiation of human promyelocytic leukemic cells in primary culture in response to retinoic acid[J]. Blood, 1981, 57(6): 1000-1004. doi: 10.1182/blood.V57.6.1000.1000

    [15]

    Feng Q, Xu M, Yu YY, et al. High-dose dexamethasone or all-trans-retinoic acid restores the balance of macrophages towards M2 in immune thrombocytopenia[J]. J Thromb Haemostasis, 2017, 15(9): 1845-1858. doi: 10.1111/jth.13767

    [16]

    Zhu X, Wang Y, Jiang Q, et al. All-trans retinoic acid protects mesenchymal stem cells from immune thrombocytopenia by regulating the complement-interleukin-1β loop[J]. Haematologica, 2019, 104(8): 1661-1675. doi: 10.3324/haematol.2018.204446

    [17]

    Dai L, Zhang R, Wang Z, et al. Efficacy of immunomodulatory therapy with all-trans retinoid acid in adult patients with chronic immune thrombocytopenia[J]. Thromb Res, 2016, 140: 73-80. doi: 10.1016/j.thromres.2016.02.013

    [18]

    Feng FE, Feng R, Wang M, et al. Oral all-trans retinoic acid plus danazol versus danazol as second-line treatment in adults with primary immune thrombocytopenia: a multicentre, randomised, open-label, phase 2 trial[J]. Lancet Haematol, 2017, 4(10): e487-e496. doi: 10.1016/S2352-3026(17)30170-9

    [19]

    Huang QS, Liu Y, Wang JB, et al. All-trans retinoic acid plus high-dose dexamethasone as first-line treatment for patients with newly diagnosed immune thrombocytopenia: a multicentre, open-label, randomised, controlled, phase 2 trial[J]. Lancet Haematol, 2021, 8(10): e688-e699. doi: 10.1016/S2352-3026(21)00240-4

    [20]

    Stasi R, Cooper N, Del Poeta G, et al. Analysis of regulatory T-cell changes in patients with idiopathic thrombocytopenic purpura receiving B cell-depleting therapy with rituximab[J]. Blood, 2008, 112(4): 1147-1150. doi: 10.1182/blood-2007-12-129262

    [21]

    Stasi R, Del Poeta G, Stipa E, et al. Response to B-cell-depleting therapy with rituximab reverts the abnormalities of T-cell subsets in patients with idiopathic thrombocytopenic purpura[J]. Blood, 2007, 110(8): 2924-2930. doi: 10.1182/blood-2007-02-068999

    [22]

    Lambert M, Gernsheimer TB. Clinical updates in adult immune thrombocytopenia[J]. Blood, 2017, 129(21): 2829-2835. doi: 10.1182/blood-2017-03-754119

    [23]

    Stasi R, Pagano A, Stipa E, et al. Rituximab chimeric anti-CD20 monoclonal antibody treatment for adults with chronic idiopathic thrombocytopenic purpura[J]. Blood, 2001, 98(4): 952-957. doi: 10.1182/blood.V98.4.952

    [24]

    Zaja F, Volpetti S, Chiozzotto M, et al. Long-term follow-up analysis after rituximab salvage therapy in adult patients with immune thrombocytopenia[J]. Am J Hematol, 2012, 87(9): 886-889. doi: 10.1002/ajh.23272

    [25]

    Patel VL, Mahévas M, Lee SY, et al. Outcomes 5 years after response to rituximab therapy in children and adults with immune thrombocytopenia[J]. Blood, 2012, 119(25): 5989-5995. doi: 10.1182/blood-2011-11-393975

    [26]

    Li Y, Shi Y, He Z, et al. The efficacy and safety of low-dose rituximab in immune thrombocytopenia: a systematic review and meta-analysis[J]. Platelets, 2019, 30(6): 690-697. doi: 10.1080/09537104.2019.1624706

    [27]

    Chaturvedi S, Arnold DM, McCrae KR. Splenectomy for immune thrombocytopenia: down but not out[J]. Blood, 2018, 131(11): 1172-1182. doi: 10.1182/blood-2017-09-742353

    [28]

    Ghanima W, Khelif A, Waage A, et al. Rituximab as second-line treatment for adult immune thrombocytopenia(the RITP trial): a multicentre, randomised, double-blind, placebo-controlled trial[J]. Lancet, 2015, 385(9978): 1653-1661. doi: 10.1016/S0140-6736(14)61495-1

    [29]

    Ferraro AJ, Drayson MT, Savage COS, et al. Levels of autoantibodies, unlike antibodies to all extrinsic antigen groups, fall following B cell depletion with Rituximab[J]. Eur J Immunol, 2008, 38(1): 292-298. doi: 10.1002/eji.200737557

    [30]

    Looney RJ, Anolik JH, Campbell D, et al. B cell depletion as a novel treatment for systemic lupus erythematosus: A phase Ⅰ/Ⅱ dose-escalation trial of rituximab[J]. Arthritis Rheu, 2004, 50(8): 2580-2589. doi: 10.1002/art.20430

    [31]

    Avilés A, Talavera A, Díaz-Maqueo JC, et al. Evaluation on a Six-Dose Treatment of Anti CD 20 Monoclonal Antibody in Patients with Refractory Follicular Lymphoma[J]. Cancer Biother Radiopharm, 2001, 16(2): 159-162.

    [32]

    Avilés A, León MI, Díaz-Maqueo JC, et al. Rituximab in the Treatment of Refractory Follicular Lymphoma-Six Doses Are Better Than Four[J]. J Hematother Stem Cell Res, 2001, 10(2): 313-316. doi: 10.1089/15258160151135088

    [33]

    Vital EM, Dass S, Buch MH, et al. An extra dose of rituximab improves clinical response in rheumatoid arthritis patients with initial incomplete B cell depletion: a randomised controlled trial[J]. Ann Rheum Dis, 2015, 74(6): 1195-1201. doi: 10.1136/annrheumdis-2013-204544

    [34]

    Miltiadous O, Hou M, Bussel JB. Identifying and treating refractory ITP: difficulty in diagnosis and role of combination treatment[J]. Blood, 2020, 135(7): 472-490. doi: 10.1182/blood.2019003599

    [35]

    Wu YJ, Liu H, Zeng QZ, et al. All-trans retinoic acid plus low-dose rituximab vs low-dose rituximab in corticosteroid-resistant or relapsed ITP[J]. Blood, 2022, 139(3): 333-342. doi: 10.1182/blood.2021013393

  • 加载中
计量
  • 文章访问数:  369
  • PDF下载数:  253
  • 施引文献:  0
出版历程
收稿日期:  2023-11-30
刊出日期:  2024-01-01

目录