472 Grandparents Are Invaluable People As HLA-Matched Donors in Hematopoietic Stem Cell Transplantation

Track: Contributed Abstracts
Saturday, February 16, 2013, 6:45 PM-7:45 PM
Hall 1 (Salt Palace Convention Center)
Amir Ali Hamidieh, M.D. , Hematology, Oncology and Stem Cell Transplantation Research center, Tehran University of Medical Sciences, Tehran, Iran
Mohammadreza Ostadali, M.D. , Hematology, Oncology and Stem Cell Transplantation Research center, Tehran University of Medical Sciences, Tehran, Iran
Maryam Behfar, M.D. , Hematology, Oncology and Stem Cell Transplantation Research center, Tehran University of Medical Sciences, Tehran, Iran
Sirous Tayebi , Hematology, Oncology and Stem Cell Transplantation Research center, Tehran University of Medical Sciences, Tehran, Iran
Ashraf sadat Hosseini , Hematology, Oncology and Stem Cell Transplantation Research center, Tehran University of Medical Sciences, Tehran, Iran
Arash Jalali , Hematology, Oncology and Stem Cell Transplantation Research center, Tehran University of Medical Sciences, Tehran, Iran
Ardeshir Ghavamzadeh, M.D. , Hematology, Oncology and Stem Cell Transplantation Research center, Tehran University of Medical Sciences, Tehran, Iran

Grandparents are invaluable people as HLA-matched donors in hematopoietic stem cell transplantation

 

Background: HLA matching is one of the most important factors affecting patients' prognosis after hematopoietic stem cell transplantation (HSCT). Currently when there are no HLA-match siblings, transplantation centers try to find unrelated HLA-matched donor through bone marrow and cord blood registries. However, few studies showed that searching extended families such as parents , grandparents, aunts and uncles for an appropriate donor is useful.

Methods: This is a retrospective study from our center in which the patients who underwent HSCT of any diseases and their grandparents were as donors included in the study. The principal data including graft-versus-host-disease (GVHD) occurrence, overall survival (OS) and disease free survival (DFS) were used as main outcomes in these transplantations.

Results: Thirteen patients including 7 boys and 6 girls with mean age 5.33 years (range: 0.25-11) were detected through the data registry bank. The mean donors' age was 61.77 years (range: 45-75) and mean age difference was 56.44 years (range: 36.5-73) [table 1]. Regarding GVHD occurrence, 10 patients did experience acute GVHD [table 1]. With median follow-up of 16 months OS and DFS were 83% and 69% respectively.

Conclusion: Although searching the extended family for HLA-matched donors especially among grandparents seems very uncommon, this can increase the chance of well-tolerated and success transplantation especially in regions where consanguinity is common.

Table 1: Patients and donors characteristics

Patient number

Age (years)

Sex

Donor Age

(years)

Donor Sex

Source of Progenitor

Age Difference(years)

Disease

Acute GVHD

Chronic GVHD

Patient Status

1

6

Male

62

Male

PB

56

ALL

Yes

No

Full chimerism/Alive

2

5

Male

60

Female

PB

55

TM II

Yes

No

Full chimerism/Alive

3

2.5

Female

45

Female

BM

42.5

LAD I

Yes

Yes

Full chimerism/Alive

4

5.5

Female

63

Male

PB

57.5

FA

Yes

No

Full chimerism/Alive

5

7

Male

75

Female

PB

68

TM II

Yes

No

Rejected/Dead

6

2

Female

60

Female

PB

58

AML

No

No

Rejected/ Alive

7

11

Male

69

Male

PB

58

FA

No

No

Full chimerism/Alive

8

8.5

Female

68

Male

PB

59.5

CD4 dif.

Yes

Yes

Full chimerism/Alive

9

9.5

Female

46

Female

BM

36.5

AML

Yes

No

Rejected/Dead

10

2

Male

48

Female

BM

46

MPS I

Yes

No

Full chimerism/Alive

11

1

Male

74

Male

PB

73

LAD I

Yes

Yes

Full chimerism/Alive

12

9

Male

62

Male

PB

53

TM III

No

No

Rejected/ Alive

13

0.25

Female

71

Male

PB

70.75

SCID

Yes

No

Full chimerism/Alive

PB: Peripheral Blood, BM: Bone Marrow, ALL: Acute Lymphoblastic Leukemia, TM: Thalassemia Major, LAD: Leukocyte Adhesion Deficiency, FA: Fanconi Anemia, CD4 dif: CD4 deficiency, AML: Acute Myeloid Leukemia, MPS: Mucopolysaccharidoses, SCID: Severe Combined Immunodeficiency