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Diagnosis and management of acquired thrombotic thrombocytopenic purpura in southeast China: a single center experience of 60 cases

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Abstract

Acquired thrombotic thrombocytopenic purpura (TTP) is a rare life-threatening thrombotic microangiopathy. This study aimed to provide a profile of the diagnosis and management of patients with acquired TTP collected in 10 years in a single center in southeast China. A total of 60 patients diagnosed with acute acquired TTP from March 2005 to August 2015 were enrolled. Among the 60 patients, 52 patients presented with their first episodes, and eight patients had two or more episodes. The median age at presentation was 49 (range, 17 to 78) years with a female predominance (male:female ratio, 1:1.60). ADAMTS 13 activity were analyzed in 43 patients, among whom 33 (76.7%) patients had a baseline level of < 5%. Mortality was 30%. Plasma exchange (PEX) was performed in 62 of 69 (89.9%) episodes. Corticosteroids were administered in 54 of 69 (78.3%) episodes. Other immunosuppressants (e.g., vincristine, cyclosporine, and cyclosporin) were used in 7 of 69 (10.1%) episodes. Rituximab was documented in 4 patients with refractory/relapsed TTP for 5 episodes, showing encouraging results. In conclusion, the diagnosis of TTP depended on a comprehensive analysis of clinical data. Plasma ADAMTS13 activity assay helped confirm a diagnosis. PEX was the mainstay of the therapy, and rituximab can be used in relapsed/refractory disease.

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References

  1. Scully M, Brown J, Patel R, McDonald V, Brown CJ, Machin S. Human leukocyte antigen association in idiopathic thrombotic thrombocytopenic purpura: evidence for an immunogenetic link. J Thromb Haemost 2010; 8(2): 2–257

    Article  CAS  Google Scholar 

  2. Zheng X, Chung D, Takayama TK, Majerus EM, Sadler JE, Fujikawa K. Structure of von Willebrand factor-cleaving protease (ADAMTS13), a metalloprotease involved in thrombotic thrombocytopenic purpura. J Biol Chem 2001; 276(44): 44–41059

    Article  Google Scholar 

  3. Sadler JE, Moake JL, Miyata T, George JN. Recent advances in thrombotic thrombocytopenic purpura. Hematology Am Soc Hematol Educ Program 2004; 2004(1): 1–407

    Google Scholar 

  4. Thrombosis, Hemostasis group HSCMA. Consensus of Chinese experts on diagnosis and treatment of thrombotic thrombocytopenic purpura (version 2012). Chin J Hematol (Zhonghua Xue Ye Xue Za Zhi) 2012; 33(11): 11–983(in Chinese)

    Google Scholar 

  5. Scully M, Hunt BJ, Benjamin S, Liesner R, Rose P, Peyvandi F, Cheung B, Machin SJ; British Committee for Standards in Haematology. Guidelines on the diagnosis and management of thrombotic thrombocytopenic purpura and other thrombotic microangiopathies. Br J Haematol 2012; 158(3): 3–323

    Article  Google Scholar 

  6. Gao WQ, Su J, Bai X, Wang ZY, Ruan CG. Evaluation of von Willebrand factor-cleaving protease activity in patients with thrombotic thrombocytopenic purpura. Chin Med J (Engl) 2004; 117(6): 6–818

    Google Scholar 

  7. Sadler JE. Von Willebrand factor, ADAMTS13, and thrombotic thrombocytopenic purpura. Blood 2008; 112(1): 1–11

    Article  CAS  Google Scholar 

  8. Chauhan AK, Motto DG, Lamb CB, Bergmeier W, Dockal M, Plaimauer B, Scheiflinger F, Ginsburg D, Wagner DD. Systemic antithrombotic effects of ADAMTS13. J Exp Med 2006; 203(3): 3–767

    Article  CAS  Google Scholar 

  9. Xiao J, Jin SY, Xue J, Sorvillo N, Voorberg J, Zheng XL. Essential domains of a disintegrin and metalloprotease with thrombospondin type 1 repeats-13 metalloprotease required for modulation of arterial thrombosis. Arterioscler Thromb Vasc Biol 2011; 31(10): 10–2261

    Article  CAS  Google Scholar 

  10. Sadler JE. What’s new in the diagnosis and pathophysiology of thrombotic thrombocytopenic purpura. Hematology Am Soc Hematol Educ Program 2015; 2015: 631–636

    PubMed  PubMed Central  Google Scholar 

  11. Terrell DR, Williams LA, Vesely SK, Lämmle B, Hovinga JA, George JN. The incidence of thrombotic thrombocytopenic purpurahemolytic uremic syndrome: all patients, idiopathic patients, and patients with severe ADAMTS-13 deficiency. J Thromb Haemost 2005; 3(7): 7–1432

    Article  Google Scholar 

  12. Scully M, Yarranton H, Liesner R, Cavenagh J, Hunt B, Benjamin S, Bevan D, Mackie I, Machin S. Regional UK TTP registry: correlation with laboratory ADAMTS 13 analysis and clinical features. Br J Haematol 2008; 142(5): 5–819

    Article  Google Scholar 

  13. Sayani FA, Abrams CS. How I treat refractory thrombotic thrombocytopenic purpura. Blood 2015; 125(25): 25–3860

    Article  CAS  Google Scholar 

  14. Hanby HA, Zheng XL. Current status in diagnosis and treatment of hereditary thrombotic thrombocytopenic purpura. Hereditary Genet 2014; 3: e108

    PubMed  PubMed Central  Google Scholar 

  15. Zhan H, Streiff MB, King KE, Segal JB. Thrombotic thrombocytopenic purpura at the Johns Hopkins Hospital from 1992 to 2008: clinical outcomes and risk factors for relapse. Transfusion 2010; 50 (4): 868–874

    Article  PubMed  Google Scholar 

  16. Deroux A, Sirodot M, Daguindau N, Barro C, Coppo P, Bouillet L. Management of thrombotic thrombocytopenic purpura in two French centers: a series of 27 patients. Rev Med Interne 2016; 37 (1): 13–18

    Article  PubMed  CAS  Google Scholar 

  17. Blombery P, Kivivali L, Pepperell D, Mc Quilten Z, Engelbrecht S, Polizzotto MN, Phillips LE, Wood E, Cohney S; TTP registry steering committee. Diagnosis and management of thrombotic thrombocytopenic purpura (TTP) in Australia: findings from the first 5 years of the Australian TTP/thrombotic microangiopathy registry. Intern Med J 2016; 46(1): 1–71

    Article  CAS  Google Scholar 

  18. Lim W, Vesely SK, George JN. The role of rituximab in the management of patients with acquired thrombotic thrombocytopenic purpura. Blood 2015; 125(10): 10–1526

    Article  CAS  Google Scholar 

  19. Coppo P, Froissart A; French Reference Center for Thrombotic Microangiopathies. Treatment of thrombotic thrombocytopenic purpura beyond therapeutic plasma exchange. Hematology Am Soc Hematol Educ Program 2015; 2015: 637–643

    PubMed  Google Scholar 

  20. Cataland SR, Wu HM. Acquired thrombotic thrombocytopenic purpura: new therapeutic options and their optimal use. J Thromb Haemost 2015; 13(Suppl 1): S223–S229

    Article  PubMed  CAS  Google Scholar 

  21. Tong HY, Ye LI, Ye XN, Lu DM, Li Y. Long-term remission induced by low-dose rituximab for relapsed and refractory thrombotic thrombocytopenic purpura: a report of two cases. Exp Ther Med 2015; 10(6): 6–2295

    Article  CAS  Google Scholar 

  22. Holz JB. The TITAN trial—assessing the efficacy and safety of an anti-von Willebrand factor Nanobody in patients with acquired thrombotic thrombocytopenic purpura. Transfus Apheresis Sci 2012; 46(3): 3–343

    Article  Google Scholar 

  23. Plaimauer B, Kremer Hovinga JA, Juno C, Wolfsegger MJ, Skalicky S, Schmidt M, Grillberger L, Hasslacher M, Knöbl P, Ehrlich H, Scheiflinger F. Recombinant ADAMTS13 normalizes von Willebrand factor-cleaving activity in plasma of acquired TTP patients by overriding inhibitory antibodies. J Thromb Haemost 2011; 9(5): 5–936

    Article  CAS  Google Scholar 

  24. Jian C, Xiao J, Gong L, Skipwith CG, Jin SY, Kwaan HC, Zheng XL. Gain-of-function ADAMTS13 variants that are resistant to autoantibodies against ADAMTS13 in patients with acquired thrombotic thrombocytopenic purpura. Blood 2012; 119(16): 16–3836

    Article  CAS  Google Scholar 

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Correspondence to Hongyan Tong.

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These authors contributed equally to this manuscript.

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Zhou, X., Ye, X., Ren, Y. et al. Diagnosis and management of acquired thrombotic thrombocytopenic purpura in southeast China: a single center experience of 60 cases. Front. Med. 10, 430–436 (2016). https://doi.org/10.1007/s11684-016-0492-5

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  • DOI: https://doi.org/10.1007/s11684-016-0492-5

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