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. 2006 Jun 15;108(8):2509–2519. doi: 10.1182/blood-2006-03-010777

Table 2.

Allogeneic sibling transplantation for severe aplastic anemia

Institution/study Years of study N Age, y (median in y) Graft rejection/failure, % Acute GVHD,*% Chronic GVHD, % Actuarial survival, %
IBMTR92 1988-1992 471 20 (1-51) 16 19 32 66 at 5 y
Vienna93 1982-1996 20 25 (17-37) 0 26 53 95 at 15 y
EBMT94 1991-1998 71 19 (4-46) 3 30 35 86 at 5 y
Seoul95 1990-1999 22 22 (14-43) 5 10 33 95 at 5 y
Seoul96 1990-2001 64 28 (14-43) 18 31 19 79 at 6 y
Hamburg97 1990-2001 21 25 (7-43) 5 5 5 86 at 5 y
Paris98 1994-2001 33 20 (8-42) 6 0 42 94 at 5 y
Sao Paulo99 1993-2001 81 24 (3-53) 22 37 39 56 at 6 y
Taipei100 1985-2001 79 22 (4-43) 8 7 35 74 at 5 y
Tunis101 1998-2001 31 19 (4-39) 16 11 3 86 at 2 y
Seoul102 1995-2001 113 28 (16-50) 15 11 12 89 at 6 y
London103 1989-2003 33 17 (4-46) 24 14 4 81 at 5 y
Seattle104,105 1988-2004 94 26 (2-59) 4 24 26 88 at 6 y
Mexico City106 2000-2005 23 25 (4-65) 26 17 26 88 at 4 y

In contrast to Table 1, response rates are not provided because, in surviving patients who do not experience primary graft rejection or secondary graft failure, full hematologic recovery with donor hematopoiesis is anticipated. Only studies reporting at least 20 patients are tabulated

GVHD indicates graft-versus-host disease; IBMTR, International Blood and Marrow Transplant Registry; and EBMT, European Group for Bone Marrow Transplant

*

Results are generally for grades II to IV and patients at risk