TY - JOUR
T1 - Management of hyperleukocytosis and impact of leukapheresis among patients with acute myeloid leukemia (AML) on short- and long-term clinical outcomes
T2 - a large, retrospective, multicenter, international study
AU - Stahl, Maximilian
AU - Shallis, Rory M.
AU - Wei, Wei
AU - Montesinos, Pau
AU - Lengline, Etienne
AU - Neukirchen, Judith
AU - Bhatt, Vijaya R.
AU - Sekeres, Mikkael A.
AU - Fathi, Amir T.
AU - Konig, Heiko
AU - Luger, Selina
AU - Khan, Irum
AU - Roboz, Gail J.
AU - Cluzeau, Thomas
AU - Martínez-Cuadron, David
AU - Raffoux, Emmanuel
AU - Germing, Ulrich
AU - Umakanthan, Jayadev Manikkam
AU - Mukherjee, Sudipto
AU - Brunner, Andrew M.
AU - Miller, Adam
AU - McMahon, Christine M.
AU - Ritchie, Ellen K.
AU - Rodríguez-Veiga, Rebeca
AU - Itzykson, Raphaël
AU - Boluda, Blanca
AU - Rabian, Florence
AU - Tormo, Mar
AU - Acuña-Cruz, Evelyn
AU - Rabinovich, Emma
AU - Yoo, Brendan
AU - Cano, Isabel
AU - Podoltsev, Nikolai A.
AU - Bewersdorf, Jan Philipp
AU - Gore, Steven
AU - Zeidan, Amer M.
N1 - Publisher Copyright:
© 2020, The Author(s), under exclusive licence to Springer Nature Limited.
PY - 2020/12
Y1 - 2020/12
N2 - Hyperleukocytosis in acute myeloid leukemia (AML) is associated with inferior outcomes. There is limited high quality evidence to support the benefits of leukapheresis. We retrospectively collected data from patients with newly-diagnosed AML who presented with a white cell count (WBC) >50 × 109/L to 12 centers in the United States and Europe from 2006 to 2017 and received intensive chemotherapy. Logistic regression models estimated odds ratios for 30-day mortality and achievement of composite complete remission (CRc). Cox proportional hazard models estimated hazard ratios for overall survival (OS). Among 779 patients, clinical leukostasis was reported in 27%, and leukapheresis was used in 113 patients (15%). Thirty-day mortality was 16.7% (95% CI: 13.9–19.3%). Median OS was 12.6 months (95% CI: 11.5–14.9) among all patients, and 4.5 months (95% CI: 2.7–7.1) among those ≥65 years. Use of leukapheresis did not significantly impact 30-day mortality, achievement of CRc, or OS in multivariate analysis based on available data or in analysis based on multiple imputation. Among patients with investigator-adjudicated clinical leukostasis, there were statistically significant improvements in 30-day mortality and OS with leukapheresis in unadjusted analysis, but not in multivariate analysis. Given the significant resource use, cost, and potential complications of leukapheresis, randomized studies are needed to evaluate its value.
AB - Hyperleukocytosis in acute myeloid leukemia (AML) is associated with inferior outcomes. There is limited high quality evidence to support the benefits of leukapheresis. We retrospectively collected data from patients with newly-diagnosed AML who presented with a white cell count (WBC) >50 × 109/L to 12 centers in the United States and Europe from 2006 to 2017 and received intensive chemotherapy. Logistic regression models estimated odds ratios for 30-day mortality and achievement of composite complete remission (CRc). Cox proportional hazard models estimated hazard ratios for overall survival (OS). Among 779 patients, clinical leukostasis was reported in 27%, and leukapheresis was used in 113 patients (15%). Thirty-day mortality was 16.7% (95% CI: 13.9–19.3%). Median OS was 12.6 months (95% CI: 11.5–14.9) among all patients, and 4.5 months (95% CI: 2.7–7.1) among those ≥65 years. Use of leukapheresis did not significantly impact 30-day mortality, achievement of CRc, or OS in multivariate analysis based on available data or in analysis based on multiple imputation. Among patients with investigator-adjudicated clinical leukostasis, there were statistically significant improvements in 30-day mortality and OS with leukapheresis in unadjusted analysis, but not in multivariate analysis. Given the significant resource use, cost, and potential complications of leukapheresis, randomized studies are needed to evaluate its value.
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U2 - 10.1038/s41375-020-0783-3
DO - 10.1038/s41375-020-0783-3
M3 - Article
C2 - 32132655
AN - SCOPUS:85080084148
SN - 0887-6924
VL - 34
SP - 3149
EP - 3160
JO - Leukemia
JF - Leukemia
IS - 12
ER -