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Post-Transplant Isoagglutinin Induced Pure Red Cell Aplasia; Incidence and Clinic Outcomes

Track: Poster Abstracts
Saturday, March 1, 2014, 6:45 PM-7:45 PM
Longhorn Hall E (Exhibit Level 1) (Gaylord Texan)
Samith Kochuparambil, MD , Division of Hematology, Mayo Clinic, Rochester, MN
Mark R Litzow, MD , Division of Hematology, Mayo Clinic, Rochester, MN
William Hogan, MBBCh , Division of Hematology, Mayo Clinic, Rochester, MN
Shahrukh Hashmi, MD , Division of Hematology, Mayo Clinic, Rochester, MN
Dennis Gastineau, MD , Division of Hematology, Mayo Clinic, Rochester, MN
Mrinal Patnaik, MD , Division of Hematology, Mayo Clinic, Rochester, MN

ABO incompatibility among patients (pts) undergoing allogeneic stem cell transplant (ASCT) is associated with delayed engraftment and post-transplant pure red cell aplasia (PT-PRCA).

After due IRB approval we retrospectively analyzed the prevalence and outcome of PT-PRCA among pts undergoing ASCT at Mayo Clinic, Rochester between 1/1/2000 and 9/30/2013. Out of 886 ASCT done during the period, we identified 53(6%) pts with major ABO and 24 (3%) pts with bi-directional ABO incompatibility. Twelve patients (1%) developed PT-PRCA; 11 had major ABO incompatibility while one had a bidirectional mismatch. All pts received red cell depleted stem cells and there were no cases of acute hemolysis. Six pts underwent reduced intensity conditioning.

Median time to diagnosis of PT-PRCA was 42 days (23-67), with reticulocytopenia and renewed transfusion dependance. Pts were initially managed with immunosuppression taper and EPO supplementation. Refractory cases were treated with plasmapheresis (4), rituximab (6) and DLI (1). One pt relapsed and 2 pts died (both sepsis) prior to resolution of PT-PRCA. After excluding these pts median time to resolution of PT-PRCA was 113 days (13-429).

PT-PRCA is not an uncommon complication of major ABO incompatible ASCT. However it is relatively less common in patients with bi-directional incompatibility. PT-PRCA results in renewed transfusion dependance. Immunosuppression taper and/or immunomodulation can serve as effective treatment strategies.


Age

Δ

Gender Mis

match

HLA

ABO

Bi Dir Mismatch

Cond.    Regimen

Stem Cell

GVHD

Grade

Pre Transplant titre

Rx

(In addition to Taper Immuno

Suppression )

PRCA Diagnosed

(Day)

Retci count

at PRCA

Diagnosis

Time to  resolution

 of PRCA

(Days)

#PRBC

After PRCA

Diagnosis

Post-Transplant Survival

(Days)

*Died

43

AML

M-->F

10/10MUD

A+/O+

Flu/Bu

PBSCT

Skin  2

256

PLX ,

Rituximab

DLI

+35

0.31

122

21

228

60

AML

M-->F

10/10MUD

A+/O+

Flu/Bu

PBSCT

No

1024

Rituximab

+23

<.28

166

12

273

38

AML

M->M

9/10MUD

A+/O+

Flu TBI

PBSCT

No

512

None

+34

<.28

109

18

225

44

AML

M-->F

10/10MRD

AB+/O+

Cy/TBI

PBSCT

No

64

Rituximab , Darbepoetin

+26

<.28

 Relapsed

NA

1043

63

AML

F-->M

10/10MRD

A+/O+

Flu/Bu

PBSCT

No

> 2048

Rituximab, Darbepoetin

+40

<.28

Transfusion

Dependent

NA

114*

57

AML

M->M

10/10MUD

A+/O+

Flu/Mel

PBSCT

Skin  1

1024

Darbepoetin

Rituximab,

PLX

+57

<.28

429

72

1583

68

AML

M->M

10/10MUD

B+/O+

Flu/Mel

PBSCT

Skin  1

1024

None

+56

<.28

145

14

867

51

ALL

M-->F

10/10MUD

A+/O+

Cy/TBI

PBSCT

No

1024

Rituximab

Darbepoetin

+52

<.28

Transfusion

Dependent

NA

315*

63

ALL

M-->F

10/10MUD

A+/O+

Cy/TBI

BMSCT

Skin  1

UK

Darbepoetin

+45

<.28

18

4

2643

47

CML

M->M

10/10MUD

B-/A+

Bi-Dir

Cy/TBI

PBSCT

No

Neg

PLX

+67

<.28

17

7

211*

41

MDS

M->M

10/10MUD

AB+/O+

Cy/Bu

PBSCT

No

256

PLX

+49

<.28

116

17

614

33

MDS

M->M

10/10MUD

A+/O+

Pent/TBI

PBSCT

GI     1

Neg

Darbepoetin

+37

<.28

13

4

431*


                                                                                                      

Disclosures:
Nothing To Disclose