TY - JOUR
T1 - Contemporary evaluation of acute myeloid leukemia patients with long-term survival exceeding 5 years
AU - Heering, Gabriel
AU - Sasson, Maya
AU - Dominissini, Dan
AU - Shimoni, Avichai
AU - Avigdor, Abraham
AU - Nagler, Arnon
AU - Canaani, Jonathan
N1 - Publisher Copyright:
© 2022 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.
PY - 2022/12
Y1 - 2022/12
N2 - Objectives: Define clinical and laboratory attributes of acute myeloid leukemia (AML) patients with long-term survival exceeding five years and compare them with AML patients succumbing to disease within 2 years of diagnosis. Methods: A retrospective analysis of AML patients alive at least five years from the time of initial diagnosis. Baseline clinical data were compared with patients who died within 2 years of diagnosis. Results: The long-term cohort consisted of 93 patients treated in 2007–2016 with a median follow-up duration of 7.7 years (range 5–13.6 years). European LeukemiaNet (ELN) 2017 favorable risk patients accounted for 60% of the cohort. All long-term survivors achieved remission following induction chemotherapy. Multivariate analysis showed that compared with 132 patients experiencing death within 2 years of diagnosis, long-term survivors were more likely to be of younger age [odds ratio (OR), 0.92; 95% confidence interval (CI), 0.9–0.95; p < 0.001], have a lower initial WBC count (OR, 0.58; 95% CI, 0.43–0.79; p = 0.0004), undergo an allogeneic stem cell transplantation (OR, 7.95; 95% CI, 3.07–20.59; p < 0.0001), and harbor favorable risk cytogenetics (OR, 0.03; 95% CI, 0.006–0.23; p = 0.0004). Conclusions: Long-term survival of AML is seen in a distinct demographic and biologic patient subset.
AB - Objectives: Define clinical and laboratory attributes of acute myeloid leukemia (AML) patients with long-term survival exceeding five years and compare them with AML patients succumbing to disease within 2 years of diagnosis. Methods: A retrospective analysis of AML patients alive at least five years from the time of initial diagnosis. Baseline clinical data were compared with patients who died within 2 years of diagnosis. Results: The long-term cohort consisted of 93 patients treated in 2007–2016 with a median follow-up duration of 7.7 years (range 5–13.6 years). European LeukemiaNet (ELN) 2017 favorable risk patients accounted for 60% of the cohort. All long-term survivors achieved remission following induction chemotherapy. Multivariate analysis showed that compared with 132 patients experiencing death within 2 years of diagnosis, long-term survivors were more likely to be of younger age [odds ratio (OR), 0.92; 95% confidence interval (CI), 0.9–0.95; p < 0.001], have a lower initial WBC count (OR, 0.58; 95% CI, 0.43–0.79; p = 0.0004), undergo an allogeneic stem cell transplantation (OR, 7.95; 95% CI, 3.07–20.59; p < 0.0001), and harbor favorable risk cytogenetics (OR, 0.03; 95% CI, 0.006–0.23; p = 0.0004). Conclusions: Long-term survival of AML is seen in a distinct demographic and biologic patient subset.
KW - Acute myeloid leukemia
KW - ELN 2017
KW - long-term survival
UR - http://www.scopus.com/inward/record.url?scp=85139037420&partnerID=8YFLogxK
U2 - 10.1111/ejh.13864
DO - 10.1111/ejh.13864
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C2 - 36128925
AN - SCOPUS:85139037420
SN - 0902-4441
VL - 109
SP - 765
EP - 771
JO - European Journal of Haematology
JF - European Journal of Haematology
IS - 6
ER -