TY - JOUR
T1 - TP53 mutations in older adults with acute myeloid leukemia
AU - Yanada, Masamitsu
AU - Yamamoto, Yukiya
AU - Iba, Sachiko
AU - Okamoto, Akinao
AU - Inaguma, Yoko
AU - Tokuda, Masutaka
AU - Morishima, Satoko
AU - Kanie, Tadaharu
AU - Mizuta, Shuichi
AU - Akatsuka, Yoshiki
AU - Okamoto, Masataka
AU - Emi, Nobuhiko
N1 - Publisher Copyright:
© 2016, The Japanese Society of Hematology.
PY - 2016/4/1
Y1 - 2016/4/1
N2 - The net benefits of induction therapy for older adults with acute myeloid leukemia (AML) remain controversial. Because AML in older adults is a heterogeneous disease, it is important to identify those who are unlikely to benefit from induction therapy based on information available at the initial assessment. We used next-generation sequencing to analyze TP53 mutation status in AML patients aged 60 years or older, and evaluated its effects on outcomes. TP53 mutations were detected in 12 of 77 patients (16 %), and there was a significant association between TP53 mutations and monosomal karyotype. Patients with TP53 mutations had significantly worse survival than those without (P = 0.009), and multivariate analysis identified TP53 mutation status as the most significant prognostic factor for survival. Neverthelsess, TP53-mutated patients had a 42 % chance of complete remission and a median survival of 8.0 months, which compares favorably with those who did not undergo induction therapy, even in the short term. These results suggest that screening for TP53 mutations at diagnosis is useful for identifying older adults with AML who are least likely to respond to chemotherapy, although the presence of this mutation alone does not seem to justify rejecting induction therapy.
AB - The net benefits of induction therapy for older adults with acute myeloid leukemia (AML) remain controversial. Because AML in older adults is a heterogeneous disease, it is important to identify those who are unlikely to benefit from induction therapy based on information available at the initial assessment. We used next-generation sequencing to analyze TP53 mutation status in AML patients aged 60 years or older, and evaluated its effects on outcomes. TP53 mutations were detected in 12 of 77 patients (16 %), and there was a significant association between TP53 mutations and monosomal karyotype. Patients with TP53 mutations had significantly worse survival than those without (P = 0.009), and multivariate analysis identified TP53 mutation status as the most significant prognostic factor for survival. Neverthelsess, TP53-mutated patients had a 42 % chance of complete remission and a median survival of 8.0 months, which compares favorably with those who did not undergo induction therapy, even in the short term. These results suggest that screening for TP53 mutations at diagnosis is useful for identifying older adults with AML who are least likely to respond to chemotherapy, although the presence of this mutation alone does not seem to justify rejecting induction therapy.
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U2 - 10.1007/s12185-016-1942-1
DO - 10.1007/s12185-016-1942-1
M3 - Article
C2 - 26781615
AN - SCOPUS:84961613498
SN - 0925-5710
VL - 103
SP - 429
EP - 435
JO - International Journal of Hematology
JF - International Journal of Hematology
IS - 4
ER -