TY - JOUR
T1 - Rapid Donor Identification Improves Survival in High-Risk First-Remission Patients with Acute Myeloid Leukemia
AU - Pagel, John M.
AU - Othus, Megan
AU - Garcia-Manero, Guillermo
AU - Fang, Min
AU - Radich, Jerald P.
AU - Rizzieri, David A.
AU - Marcucci, Guido
AU - Strickland, Stephen A.
AU - Litzow, Mark R.
AU - Lynn Savoie, M.
AU - Spellman, Stephen R.
AU - Confer, Dennis L.
AU - Chell, Jeffrey W.
AU - Brown, Maria
AU - Medeiros, Bruno C.
AU - Sekeres, Mikkael A.
AU - Lin, Tara L.
AU - Uy, Geoffrey L.
AU - Powell, Bayard L.
AU - Bayer, Ruthee Lu
AU - Larson, Richard A.
AU - Stone, Richard M.
AU - Claxton, David
AU - Essell, James
AU - Luger, Selina M.
AU - Mohan, Sanjay R.
AU - Moseley, Anna
AU - Erba, Harry P.
AU - Appelbaum, Frederick R.
N1 - Publisher Copyright:
Copyright © 2020 American Society of Clinical Oncology. All rights reserved.
PY - 2020/6/1
Y1 - 2020/6/1
N2 - PURPOSE Patients with acute myeloid leukemia with high-risk cytogenetics in first complete remission (CR1) achieve better outcomes if they undergo allogeneic hematopoietic cell transplantation (HCT) compared with consolidation chemotherapy alone. However, only approximately 40% of such patients typically proceed to HCT. METHODS We used a prospective organized approach to rapidly identify donors to improve the allogeneic HCT rate in adults with high-risk acute myeloid leukemia in CR1. Newly diagnosed patients had cytogenetics obtained at enrollment, and those with high-risk cytogenetics underwent expedited HLA typing and were encouraged to be referred for consultation with a transplantation team with the goal of conducting an allogeneic HCT in CR1. RESULTS Of 738 eligible patients (median age, 49 years; range, 18-60 years of age), 159 (22%) had high-risk cytogenetics and 107 of these patients (67%) achieved CR1. Seventy (65%) of the high-risk patients underwent transplantation in CR1 (P, .001 compared with the historical rate of 40%). Median time to HCT from CR1 was 77 days (range, 20-356 days). In landmark analysis, overall survival (OS) among patients who underwent transplantation was significantly better compared with that of patients who did not undergo transplantation (2-year OS, 48% v 35%, respectively [P = .031]). Median relapse-free survival after transplantation in the high-risk cohort who underwent transplantation in CR1 (n = 70) was 11.5 months (range, 4-47 months), and median OS after transplantation was 14 months (range, 4-44 months). CONCLUSION Early cytogenetic testing with an organized effort to identify a suitable allogeneic HCT donor led to a CR1 transplantation rate of 65% in the high-risk group, which, in turn, led to an improvement in OS when compared with the OS of patients who did not undergo transplantation.
AB - PURPOSE Patients with acute myeloid leukemia with high-risk cytogenetics in first complete remission (CR1) achieve better outcomes if they undergo allogeneic hematopoietic cell transplantation (HCT) compared with consolidation chemotherapy alone. However, only approximately 40% of such patients typically proceed to HCT. METHODS We used a prospective organized approach to rapidly identify donors to improve the allogeneic HCT rate in adults with high-risk acute myeloid leukemia in CR1. Newly diagnosed patients had cytogenetics obtained at enrollment, and those with high-risk cytogenetics underwent expedited HLA typing and were encouraged to be referred for consultation with a transplantation team with the goal of conducting an allogeneic HCT in CR1. RESULTS Of 738 eligible patients (median age, 49 years; range, 18-60 years of age), 159 (22%) had high-risk cytogenetics and 107 of these patients (67%) achieved CR1. Seventy (65%) of the high-risk patients underwent transplantation in CR1 (P, .001 compared with the historical rate of 40%). Median time to HCT from CR1 was 77 days (range, 20-356 days). In landmark analysis, overall survival (OS) among patients who underwent transplantation was significantly better compared with that of patients who did not undergo transplantation (2-year OS, 48% v 35%, respectively [P = .031]). Median relapse-free survival after transplantation in the high-risk cohort who underwent transplantation in CR1 (n = 70) was 11.5 months (range, 4-47 months), and median OS after transplantation was 14 months (range, 4-44 months). CONCLUSION Early cytogenetic testing with an organized effort to identify a suitable allogeneic HCT donor led to a CR1 transplantation rate of 65% in the high-risk group, which, in turn, led to an improvement in OS when compared with the OS of patients who did not undergo transplantation.
UR - http://www.scopus.com/inward/record.url?scp=85086354395&partnerID=8YFLogxK
U2 - 10.1200/JOP.19.00133
DO - 10.1200/JOP.19.00133
M3 - Article
C2 - 32048933
AN - SCOPUS:85086354395
SN - 2688-1527
VL - 16
SP - E464-E475
JO - JCO Oncology Practice
JF - JCO Oncology Practice
IS - 6
ER -