1 apl is a highly curable disease in atra ato era
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1 APL is a highly curable disease in ATRA/ATO era ATO+ATRA+CT PML - PowerPoint PPT Presentation

1 APL is a highly curable disease in ATRA/ATO era ATO+ATRA+CT PML ATO Apoptosis ATRA+CT RARa ATRA Differentiation CT Chen SJ, et al. Blood 2011;117:6425 Coagulation abnormalities is fatal for APL t(15;17) DIC PML/RARa DNR+Ara-C


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  2. APL is a highly curable disease in ATRA/ATO era ATO+ATRA+CT PML ATO Apoptosis ATRA+CT RARa ATRA Differentiation CT Chen SJ, et al. Blood 2011;117:6425

  3. Coagulation abnormalities is fatal for APL t(15;17) DIC PML/RARa DNR+Ara-C 促凝 颗粒 I Cunningham, et al. Blood 1989 ;73:1116

  4. Early death is 5-30% and majorly caused by hemorrhage 4

  5. Incidence of Bleeding 5

  6. Incidence of Thrombosis 6

  7. The mechanism of coagulation abnormality in APL 7

  8. Question • Whether oral arsenic and ATRA can ameliorate coagulopathy in APL? • Is there any difference of impact on coagulopathy between oral vs iv. arsenic 8

  9. Purpose • to evaluate the impact of oral arsenic (the realgar-indigo naturalis formula, RIF) + ATRA on coagulopathy in APL compared with intravenous ATO+ATRA during induction. 9

  10. Methods Mitoxantron 2-4mg,d 4-8 Hong-Hu Zhu , et al. JCO 2013; 31 : 4215 10

  11. Results • Period: 2007-2012 • 83 patients in our center(45 oral, 38 IV.) • Hemostasis analysis during induction 11

  12. Diagnostic Criteria of Disseminated Intravascular Coagulation ≥ Taylor FB, et al. Thrombosis and Haemostasis. 2001;86:1327-30 12

  13. Characteristics of APL patients 13

  14. Comparison of the dynamic changes of hemostatic parameters between the RIF and ATO groups 14

  15. Comparison of the dynamic changes of hemostatic parameters in DIC Score=4 15

  16. Platelet kinetics in DIC score=4 16

  17. Platelet kinetics in DIC score=4 17

  18. Conclusion • RIF +ATRA therapy ameliorate coagulopathy rapidly in APL patients • • RIF shows a significant beneficial effect in accelerating the recovery of thrombocytopenia and hypofibrinogenemia for subclinical DIC patients. 18

  19. Acknowledgements • All the patients involved in this study • My colleagues 19

  20. Thanks for your attention

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