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Rituximab for Autoimmune Diseases

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HPI: 56 bf, admitted 9/2003 w 1 wk of fatigue, nausea, anorexia, ... MRI punctate brain hemorrhages diffusely. Found unresponsive later, expired. Refractory TTP ... – PowerPoint PPT presentation

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Title: Rituximab for Autoimmune Diseases


1
Rituximab for Autoimmune Diseases
  • Case descriptions
  • Published experience
  • Mechanism of action
  • Questions
  • No financial disclosures
  • Off label use of rituximab

2
Evans Syndrome
HPI 56 bf, admitted 9/2003 w 1 wk of fatigue,
nausea, anorexia, lightheadedness PH SLE
5/2002, not active PE afebrile, 63, 179,
petechiae/purpura BLE Lab hgb 4.5, plt 6K, LDH
1270, Cr 1.5, retic 18.9, many sphero, rare
schisto ANA 15120 speckled, anti-DNA 123.4, DAT
pos IgG, Indirect neg U/A 5 rbc, 1
pro Hospital course Pred, plt rbc transfusions.
On day 4 IVIG AMS. MRI punctate brain
hemorrhages diffusely. Found unresponsive later,
expired.
3
Refractory TTP
HPI 25 bf, admit 8/2005 w 2 d n/v, bloody
emesis, petechiae, headache, nosebleed. PH TTP
3/2001, ADAMTS13 lt5, inhibitor 5 U/ml at CR,
ADAMTS13 lt5, inhibitor 16 U/ml PE afebrile,
62, 180, petechiae arms, chest, neck Lab hgb
12.2, plt 9K, LDH 1898, Cr 1.8, many schisto,
some sphero, u/a gt50 rbc, 3 protein, DAT neg,
ADAMTS13 lt4, Inh gt 8 U/ml Hospital course Pred,
PE. Day 3 comatose. CT neg. Rituximab. V tach,
seizures, bleeding, oliguric RF, DIC. Day 25
ADAMTS13 lt4, inh 1.1 U/ml. Expired.
4
Responsive TTP
HPI 62 bf, admitted w AMS, aphasia, ataxia,
falling PH None significant PE afebrile, 68,
249, petechiae arms, chest, neck Lab hgb 7.3,
plt 19K, LDH 1719, Cr 1.2, many schistocytes,
u/a 0 rbc, 3 protein, casts DAT neg, ADAMTS13
lt4, Inh 0.9 U/ml Hospital course Prednisone,
PE, plus 4 wks of VCR, rituximab. Day 31
discharged w LDH 303, plts 208K, ADAMTS13 lt4,
inhibitor 1.1 U/ml. Follow up Day 120, ADAMTS13
gt67
5
Autoimmune Cytopenias
  • Patient 1 Evans Syndrome or TTP AIHA
  • Patient 2 CR w persistent ADAMTS13 deficiency
    and high-titer inhibitor fatal relapse at 4
    years refractory to rituximab
  • Patient 3 CR w persistent ADAMTS13 deficiency
    normal ADAMTS13 at 3 months after rituximab

6
Rituximab for ITP
7
Demographics and Responses
8
Time Course of Responses
9
Responders Non-Responders
10
Adverse Events
  • 9 SAEs in 6 of 36 patients (17)
  • 2 NR serum sickness
  • 1 NR CTC grade 2 hypotension w dose 3
  • 1 CR primary varicella w dose 1
  • 1 NR hosp w grade 4 bleeding Rx IVIG
  • 1 NR hosp x4 w bleeding
  • CTC grade 1-2 chills, fever, resp sx w dose 1 in
    17 of 36 patients (47)

11
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12
Persistent ADAMTS13 Deficiency in TTP
13
Primary TTP
3
7
6
8
14
Primary TTP
10
11
12
15
Relapsing TTP
23
21
17
16
Idiopathic TTP Clinical Course
20 dead within with 5 weeks 80 complete
response in average of 16 days (range, 3-36) 40
of responders have exacerbations within first
week after initial CR 30 of responders relapse
within 2 years
Rock et al, New Eng J Med 1991 325 393-397
17
(No Transcript)
18
Clinical Characteristics
19
Inhibitors Predict Delayed Response
20
ADAMTS13 Clinical Correlations
21
ADAMTS13 Clinical Correlations
  • ADAMTS13 deficiency (lt5) predicts
  • Idiopathic TTP
  • CR to plasma exchange
  • Survival
  • ADAMTS13 inhibitor predicts
  • Prolonged time to CR
  • Relapse
  • Death

22
Rituximab in TTP
23
Patient Characteristics
24
Short-Term Outcomes
25
ADAMTS13 after Rituximab
26
Rituximab for Refractory TTP
  • At least 18 reports, 43 patients failed PE, many
    failed steroids, vincristine, splenectomy
  • Rituximab 375 mg/m2 weekly, up to 8 doses
  • Responses in 2-5 weeks
  • 38 durable complete responses
  • 2 late relapses, 1 achieved CR upon retreatment
  • 1 partial response
  • 2 no response (one with lung cancer)

27
Rituximab Mechanisms
28
Rituximab Mechanisms
  • Killing of CD20-positive cells
  • Phagocytosis
  • Complement-mediated lysis
  • Antibody-dependent cytotoxicity
  • Apoptosis induction (signaling)
  • But plasma cells lack CD20
  • Killing depends on natural apoptotic death

29
Rituximab Mechanisms
  • Most plasma cells live lt 2 weeks
  • Primary Ab responses cease in days to weeks
  • Can be replenished from memory B cells
  • Reside in spleen, nodes gt marrow
  • Some plasma cells live for years
  • Repeated immunization, T-dependent Ag
  • Require survival signals (cytokines, etc)
  • Reside in marrow, gut gt spleen, nodes

30
Questions
  • Why IVIG often helps ITP but not TTP?
  • Why (CRPR) 40 in ITP, CR 90 in TTP
  • Platelet clearance harder to block than ADAMTS13
    inhibition?
  • Why ITP and TTP responses in 2-5 weeks
  • Bad antibody is limiting, rapidly decreases?
  • Rituximab-lymphocytes clog the RE system?

31
Questions
  • Best use of ADAMTS13 assays
  • Confirm mechanism (Evans S. versus TTP)?
  • How to treat persistent ADAMTS13 deficiency
  • Preemptive immunosuppression?
  • How to kill long-lived plasma cells?
  • TRAIL agonists, bortezomib, anti-BLIMP1, et al?
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