TY - JOUR
T1 - Risk score to predict event-free survival after hematopoietic cell transplant for sickle cell disease
AU - Brazauskas, Ruta
AU - Scigliuolo, Graziana M.
AU - Wang, Hai Lin
AU - Cappelli, Barbara
AU - Ruggeri, Annalisa
AU - Fitzhugh, Courtney D.
AU - Hankins, Jane S.
AU - Kanter, Julie
AU - Meerpohl, Joerg J.
AU - Panepinto, Julie A.
AU - Rondelli, Damiano
AU - Shenoy, Shalini
AU - Walters, Mark C.
AU - Wagner, John E.
AU - Tisdale, John F.
AU - Gluckman, Eliane
AU - Eapen, Mary
N1 - Publisher Copyright:
© 2020 American Society of Hematology. All rights reserved.
PY - 2020/7/30
Y1 - 2020/7/30
N2 - We developed a risk score to predict event-free survival (EFS) after allogeneic hematopoietic cell transplantation for sickle cell disease. The study population (n 5 1425) was randomly split into training (n 5 1070) and validation (n 5 355) cohorts. Risk factors were identified and validated via Cox regression models. Two risk factors of 9 evaluated were predictive for EFS: age at transplantation and donor type. On the basis of the training cohort, patients age 12 years or younger with an HLA-matched sibling donor were at the lowest risk with a 3-year EFS of 92% (score, 0). Patients age 13 years or older with an HLA-matched sibling donor or age 12 years or younger with an HLA-matched unrelated donor were at intermediate risk (3-year EFS, 87%; score, 1). All other groups, including patients of any age with a haploidentical relative or HLA-mismatched unrelated donor and patients age 13 years or older with an HLA-matched unrelated donor were high risk (3-year EFS, 57%; score, 2 or 3). These findings were confirmed in the validation cohort. This simple risk score may guide patients with sickle cell disease and hematologists who are considering allogeneic transplantation as a curative treatment relative to other available contemporary treatments.
AB - We developed a risk score to predict event-free survival (EFS) after allogeneic hematopoietic cell transplantation for sickle cell disease. The study population (n 5 1425) was randomly split into training (n 5 1070) and validation (n 5 355) cohorts. Risk factors were identified and validated via Cox regression models. Two risk factors of 9 evaluated were predictive for EFS: age at transplantation and donor type. On the basis of the training cohort, patients age 12 years or younger with an HLA-matched sibling donor were at the lowest risk with a 3-year EFS of 92% (score, 0). Patients age 13 years or older with an HLA-matched sibling donor or age 12 years or younger with an HLA-matched unrelated donor were at intermediate risk (3-year EFS, 87%; score, 1). All other groups, including patients of any age with a haploidentical relative or HLA-mismatched unrelated donor and patients age 13 years or older with an HLA-matched unrelated donor were high risk (3-year EFS, 57%; score, 2 or 3). These findings were confirmed in the validation cohort. This simple risk score may guide patients with sickle cell disease and hematologists who are considering allogeneic transplantation as a curative treatment relative to other available contemporary treatments.
UR - http://www.scopus.com/inward/record.url?scp=85089126120&partnerID=8YFLogxK
U2 - 10.1182/blood.2020005687
DO - 10.1182/blood.2020005687
M3 - Article
C2 - 32518950
AN - SCOPUS:85089126120
SN - 0006-4971
VL - 136
SP - 623
EP - 626
JO - Blood
JF - Blood
IS - 5
ER -