TY - JOUR
T1 - Effect of donor characteristics on haploidentical transplantation with posttransplantation cyclophosphamide
AU - McCurdy, Shannon R.
AU - Zhang, Mei Jie
AU - St Martin, Andrew
AU - Al Malki, Monzr M.
AU - Bashey, Asad
AU - Gaballa, Sameh
AU - Keesler, Daniel A.
AU - Hamadani, Mehdi
AU - Norkin, Maxim
AU - Perales, Miguel Angel
AU - Reshef, Ran
AU - Rocha, Vanderson
AU - Romee, Rizwan
AU - Solh, Melhem
AU - Urbano-Ispizua, Alvaro
AU - Waller, Edmund K.
AU - Fuchs, Ephraim J.
AU - Eapen, Mary
N1 - Publisher Copyright:
© 2018 by The American Society of Hematology.
PY - 2018/2/14
Y1 - 2018/2/14
N2 - We studied the association between non-HLA donor characteristics (age, sex, donorrecipient relationship, blood group [ABO] match, and cytomegalovirus [CMV] serostatus) and transplant outcomes after T-cell-replete HLA-haploidentical transplantation using posttransplantation cyclophosphamide (PT-Cy) in 928 adults with hematologicmalignancy transplanted between 2008 and 2015. Siblings (n = 358) and offspring (n = 450) were the predominant donors, with only 120 patients having received grafts from parents. Although mortality risks were higher with donors aged 30 years or older (hazard ratio, 1.39; P < .0001), the introduction of patient age to the Cox regression model negated the effect of donor age. Two-year survival adjusted for CMV seropositivity, disease, and disease risk index was lower in patients aged 55 to 78 years after transplantation of grafts from donors younger than 30 years (53%) or aged at least 30 years (46%) compared with younger patients who received grafts from donors younger than 30 years (61%) and at least 30 years (60%; P < .0001). Similarly, 2-year survival in patients aged 55 to 78 years was lower after transplantation of grafts from siblings (45%) or offspring (48%) compared with patients aged 18 to 54 years after transplantation of grafts from siblings (62%), offspring (58%), and parents (61%; P < .0001). Graft failure was higher after transplantation of grafts from parents (14%) compared with siblings (6%) or offspring (7%; P = .02). Other non-HLA donor characteristics were not associated with survival or graft failure. The current analyses suggest patient and disease, rather than non-HLA donor characteristics, predominantly influence survival in adults.
AB - We studied the association between non-HLA donor characteristics (age, sex, donorrecipient relationship, blood group [ABO] match, and cytomegalovirus [CMV] serostatus) and transplant outcomes after T-cell-replete HLA-haploidentical transplantation using posttransplantation cyclophosphamide (PT-Cy) in 928 adults with hematologicmalignancy transplanted between 2008 and 2015. Siblings (n = 358) and offspring (n = 450) were the predominant donors, with only 120 patients having received grafts from parents. Although mortality risks were higher with donors aged 30 years or older (hazard ratio, 1.39; P < .0001), the introduction of patient age to the Cox regression model negated the effect of donor age. Two-year survival adjusted for CMV seropositivity, disease, and disease risk index was lower in patients aged 55 to 78 years after transplantation of grafts from donors younger than 30 years (53%) or aged at least 30 years (46%) compared with younger patients who received grafts from donors younger than 30 years (61%) and at least 30 years (60%; P < .0001). Similarly, 2-year survival in patients aged 55 to 78 years was lower after transplantation of grafts from siblings (45%) or offspring (48%) compared with patients aged 18 to 54 years after transplantation of grafts from siblings (62%), offspring (58%), and parents (61%; P < .0001). Graft failure was higher after transplantation of grafts from parents (14%) compared with siblings (6%) or offspring (7%; P = .02). Other non-HLA donor characteristics were not associated with survival or graft failure. The current analyses suggest patient and disease, rather than non-HLA donor characteristics, predominantly influence survival in adults.
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U2 - 10.1182/bloodadvances.2017014829
DO - 10.1182/bloodadvances.2017014829
M3 - Article
C2 - 29440002
AN - SCOPUS:85050645336
SN - 2473-9529
VL - 2
SP - 299
EP - 307
JO - Blood advances
JF - Blood advances
IS - 3
ER -