Literature DB >> 26781615

TP53 mutations in older adults with acute myeloid leukemia.

Masamitsu Yanada1, Yukiya Yamamoto2, Sachiko Iba2, Akinao Okamoto2, Yoko Inaguma2, Masutaka Tokuda2, Satoko Morishima2, Tadaharu Kanie2, Shuichi Mizuta2, Yoshiki Akatsuka2, Masataka Okamoto2, Nobuhiko Emi2.   

Abstract

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.

Entities:  

Keywords:  Acute myeloid leukemia; Monosomal karyotype; Older adults; TP53

Mesh:

Substances:

Year:  2016        PMID: 26781615     DOI: 10.1007/s12185-016-1942-1

Source DB:  PubMed          Journal:  Int J Hematol        ISSN: 0925-5710            Impact factor:   2.490


  34 in total

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7.  Impact of pretransplant measurable residual disease on the outcome of allogeneic hematopoietic cell transplantation in adult monosomal karyotype AML.

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