ACQUIRED HEMOPHILIA A M. Ellis · Acquired haemophilia literature • Randomized controlled trial...
Transcript of ACQUIRED HEMOPHILIA A M. Ellis · Acquired haemophilia literature • Randomized controlled trial...
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ACQUIRED HEMOPHILIA AACQUIRED HEMOPHILIA ACase descriptions
and a current approach to management
Martin H Ellis MD
Hematology Institute and Blood BankMeir Medical Center
IsSTH November 2012
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Patient #1Patient #1
• 78 year old man• Prostate cancerProstate cancer• Admitted with extensive subcutaneous b i i d ibruising and anemia
• PT normal, PTT >150 sec,• Mixing study – no correction of PTT• F VIII activity=5%• BU= 16BU 16
»Dg: Acquired hemophilia A
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Patient #1Patient #1
• Rapid clinical deterioration• GI bleedingGI bleeding• Treated with methylprednisolone and red cell
f itransfusions• Supportive measures institutedpp• Died within 1 week
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Patient #2
• 64 year‐old woman64 year old woman• Macroscopic hematuria• Leg and arm bruising• No previous Hx of bleeding• No previous Hx of bleeding• PT normal, PTT > 100 sec• Clinical suspicion of acquired deficiency• Mixing study failed to correct• Mixing study failed to correct• F VIII=15% and BU=4
»Dg: Acquired hemophilia A
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Patient #2Patient #2
• No hemostatic agents given• Prednisone and Cyclophosphamide startedPrednisone and Cyclophosphamide started• Resolution of bleeding• Increase in F VIII – normal within 3 weeks• Drugs tapered over 6 week periodDrugs tapered over 6 week period• Stable ( 9 months after diagnosis)
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Patient #3Patient #3
• 78 year‐old woman• History of MDS (? CMML) – mild, untreatedHistory of MDS (? CMML) mild, untreated• (Mild) dementia• CHF, obesity, hypertension• Fell at home ‐minor traumaFell at home minor trauma
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Patient #3Patient #3
• Platelets = 110K –stable• Ortho called heme consult• PT normal PTT=90 secPT normal, PTT=90 sec• Mixing study failed to correct• F VIII activity= 6%• BU= 8• BU= 8
»Dg: Acquired hemophilia A»Dg: Acquired hemophilia A
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Patient #3Patient #3
• Treatment: prednisone & cyclophosphamide• Red cell transfusionsRed cell transfusions• Extensive bruising after BP measurements, blood ddraws
• Poor venous access• Pulmonary congestion• Single dose of F VIII• rFVIIa 90 µg/kg periprocedure (PICC line)rFVIIa 90 µg/kg periprocedure (PICC line)
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August 2012August 2012
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Patient #3Patient #3
• Gradual stabilizationPTT d d ti li d• PTT decreased over time normalized
• Prednisone and Cyclophosphamide tapered y p p pover 6 weeks
• Skin defect on dorsum of hand conservatively• Skin defect on dorsum of hand‐conservatively managed
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November 2012November 2012
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November 2012November 2012
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Background•Bleeding disorder caused by an auto‐antibody to factor VIII•Severe bleedingSevere bleeding Soft tissue and mucosal bleedingFVIII level poor guide to bleeding riskFVIII level poor guide to bleeding riskHigh morbidity and mortality
•Patient group•Patient groupElderlyCo morbiditiesCo‐morbidities
•Presentation to non‐specialistsDi i d d lDiagnostic and treatment delayDifficulties transferring patients to specialist centers
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Acquired haemophilia literature• Randomized controlled trial Single published study Green T&H 70:753‐757,1995g p y• Insufficient patients to draw conclusions
• Cohort study• UKHCDO consecutive cohort Blood 109:1870‐77,2007
• Meta‐analysis• Meta analysis Delgardo et al B J H 121 21 35 2003• Meta‐analysis Delgardo et al Br J Haem 121:21‐35,2003(Publication bias of more severe patients and good outcomes)
• Registry– European Acquired Haemophilia (EACH2) Registry
Blood 120:39‐46,2012Blood 120:47‐55,2012
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Associated Conditions in AHAHemotological; Chronic lymphocytic leukemia, multiple myeloma, Waldenstrom Macroglobulinemia, non-Hodgkin lymphoma, myelodyplasia myelofibrosis
Malignancies
myelodyplasia, myelofibrosisSolid tumors:Prostate,pancreas,colon,lung,stomach,melanoma,breast,kidney,cervix,head, and neck
Systemic lupus erythematosis, rheumatoid arthritis, temporal arteritis, ulcerative colitis, Sjogren syndrome, Goodpasture syndrome, multiple sclerosis, myasthenia gravis, graft-versus-host disease autoimmune thyroid disorders and
Autoimmune disorders
versus host disease,autoimmune thyroid disorders, and autoimmune hemolytic anemia
Rarely during pregnancy, usually 1 to 4mo postpartumPregnancy-related
Beta-lactam antibiotics,chloramphenicol,sulfa drugs, phenytoin, methyldopa,interferon-a, depot thioxanthene,NSAIDs,fludarabine,clopidogrel, and BCG
Drug-induced
Psoriasis and pemphigusDermatological diseases
Acute hepatitis B and C chronic obsructive pulmonaryOth di Acute hepatitis B and C, chronic obsructive pulmonary disease, asthma, MGUS, and polymyalgia rheumatica
Other diseases
Sem Thromb hemostasis 2012
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IncidenceIncidence• Estimated incidence in defined populations
Wales1 :1 34/million/year– Wales1 :1.34/million/year– UK2 1:48/million/year
• Assuming similar incidence throughout Europe– EACH2 recruited 15% of European patients over 6 years3EACH2 recruited 15% of European patients over 6 years
1. Br J Haem 124:86‐90,20042. Blood 109:1870‐77,2007,3. JTH10:622‐31,2012
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Fatal bleeds
1981 Green 22%
2007 UKHCDO 8%
2012 EACH2 3%
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Fatal bleeding in acquired hemophilia: UKHCDO study
INHIBITOR TITER AT F VIII AT PRESENTATIONSITE OF FATAL BLEEDTIME OF DEATH AFTER PRESENTATIONPRESENTATION
NOT STATED<1GI0
24GI2
54LUNG4
154INTRACRANIAL14
89POSTOP17
182RETROPERITONEAL19
1.49INTRACRANIAL24
2195GI66
64GI106109<1INTRACRANIAL136142RETROPERITONEAL148412MULTIPLENOT STATED
• Patients at risk of fatal bleeding until inhibitor eradicated• Patients at risk of fatal bleeding until inhibitor eradicated• FVIII level and lack of bleeding at presentation does not protect against fatal bleeding
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Diagnostic pitfallsDiagnostic pitfalls
FVIII i hibi i d d• FVIII inhibitors are time dependent– Incubation of 50/50 mix for 2 hours
• All intrinsic factors may appear low– Inhibition of FVIII by the inhibitor in intrinsic factor assays
– Dilution restores factor levels due to non‐specific inhibition
• Lupus anticoagulant may interfere with factor assays
• Refer sample to a reference laboratory
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Diagnostic delay:Diagnostic delay:
• Patients are often put at unnecessary risk of severe bleedingg
B d i d• Better education and awareness
• Role of laboratory to further investigate l d i t t ltsamples and interpret results
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Management principlesManagement principles
• Early and rapid diagnosis• Avoid iatrogenically induced bleedsAvoid iatrogenically induced bleeds
– Limit venepuncture and BP monitoringN i i d l i l– No invasive procedures unless essential
• Control bleedingg– Bypassing agents
• Eradicate the inhibitor• Eradicate the inhibitor– Immunosupperssion
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Treatment of bleeding: principles• Some bleeds do not need treatment
20 30%– 20‐30%– Subcutaneous bruising rarely needs treatment
• Majority of bleeds need early treatment– NB thrombotic risk of agentsg
• OptionsBypassing agents– Bypassing agents
rFVIIa or FEIBA
– Raising factor VIIIFactor VIII/DDAVP/F VIII and immunoadsorption
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Thrombotic adverse eventsVTEMICVATotal N(%)
1269 (6 5)S 139 1269 (6.5)Sumner n=139Only rFVIIa
56112(3 9)EACH2 n=307 56112(3.9)EACH2 n=307rFVIIa,FEIBA,FVIII and DDAVP
EACH2 data
rFVIIa 5/174 (2.9%) Caution with dosingFEIBA 3/63 (4.8%) Avoid rFVIIa 270 mcg/kgFEIBA 3/63 (4.8%) Avoid rFVIIa 270 mcg/kgFVIII/DDAVP 0/70 (0%)No data 4
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Inhibitor eradication in AHAInhibitor eradication in AHA
Th i l i i i i AHA i• The optimal immunosuppressive regimen in AHA is unknown
M i– Most common regimens are• Steroids alone• Steroids and cyclophosphamide• Rituximab based regimens
– Outcome is a balance between• Inhibitor eradication • Adverse effects, including death• Risk of relapseRisk of relapse
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Analysis of Immunosuppressive regimens EACH2
l l d• First line regimens analysed– Steroids alone– Steroids and cyclophosphamideSteroids and cyclophosphamide– Rituximab based regimens
• Definitions– Complete remission (CR)
Inhibitor negative, FVIII>70 IU/dL and immunosuppression stoppedstopped
– RelapseRecurrence of inhibitor after CR
– Stable remissionCR with no relapse after immunosuppression stopped
Blood epub 18 th April 2012
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Hemostatic
RecommendedFVIII bypassing agents- rFVIIa (90-120µg./kg every 2-3 hrs)
PCC (50 100 i /k 8 12 h )Treatment - aPCC (50-100 iu/kg every 8-12 hrs)
Alternative: (if bypassing agents unavailable)-human FVIII concentrate
Bleeding-Desmopressin
Salvage treatmentImmunoadsorption/plasmapheresis
InhibitorEradication
Recommended
Prednisone (1 mg/kg/d 4-6 wks) alone or Eradication(IST)Diagnosis
Of AHA
( g g )in combination with cyclophosphanide (1.5-2 mg/kg/d maximum 5 wks)
line treatment-Second
N bl di
-Rituximab (375 mg/m2 weekly for 4 weeks) usually in association with steroids.Alternative second-line treatmentCyclosporine, azathioprine,
h l i i iNo bleeding mycophenolate, vincristine
Not recommendedHigh- dose immunoglobulins
Haematologica 2009
Identification and treatment of underlying conditions
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ConclusionsConclusions
• Early diagnosis– Education– Laboratory
• Early treatment of bleeds with bypassing agent• Early treatment of bleeds with bypassing agent– Not all bleeds need treatment– Thrombotic events are seen
• Immunosuppression as soon as diagnosis made– Optimal regimen debated– Cyclophosphamide prednisone seems preferableCyclophosphamide, prednisone seems preferable