Developing Applicable and Cost-Efficient Screens for Early Detection of AML

• Published in: Blood 2018-11, Vol.132 (Supplement 1), p.90-90
• Main Authors: Abelson, Sagi, Ng, Stanley W.K., Wang, Ting Ting, Bratman, Scott V., Dick, John E.
• Format: Article
• Language: English
• ISSN: 0006-4971; 1528-0020
• DOI: 10.1182/blood-2018-99-113403

Introduction The limited improvement of acute myeloid leukemia (AML) patient survival rates over the last few decades reveals that the strategy of targeting AML after diagnosis provides limited success. In many solid cancers, early detection leads to decreased morbidity and improved survival suggesting that a similar approach may benefit AML patients. Recently, we showed that the initial genomic events that drive AML can be detected years before diagnosis and that individuals at increased risk share distinct features that differentiate them from those with benign age related clonal hematopoiesis (ARCH). However, the relative high incidence of ARCH and the low incidence of AML, along with the fact that ARCH is recurrently being driven by mutations that occur in genes associated with AML, impedes complete discrimination. High sequencing costs for the relative large number of mutated genes implicated with the disease further hinders clinical adaptation. Therefore, a better strategic approach that is focussed on the most informative mutations and the development of accurate tools for data mining would better estimate the risk for AML development and create applicable and cost-efficient screens for early detection of AML. Methods We hypothesize that the majority of the power to accurately predict the development of AML can be derived by a minimal number of pre-leukemic hotspot mutations (pLHM) and that improved accuracy of mutation calling algorithms will increase the discrimination between high and low risk cases. We developed a novel approach to differentiate technical errors from true mutations by accounting for local sequence features to derive contextual error signatures. We demonstrate that Error Correction by Signatures Integration (ECSI) detects mutations at a higher sensitivity and specificity when compared to other techniques. 320 blood samples taken years before AML diagnosis and 856 controls were interrogated for the presence of pLHM. This data was used to construct an AML prediction model that was tuned to achieve 100% positive predictive value. To estimate the frequency of individuals at the highest risk for AML development in the general population, we applied the model to a total of 42,838 individuals whose blood was sequenced in four independent ARCH studies. Results ECSI revealed that some pLHM lie within signatures with particularly high error rates. For example, DNMT3A-R882H is defined by the signature G[C>T]G that has the highest sequencing