| Literature DB >> 28092685 |
Moritz Gerstung1,2, Elli Papaemmanuil1,3, Inigo Martincorena1, Lars Bullinger4, Verena I Gaidzik4, Peter Paschka4, Michael Heuser5, Felicitas Thol5, Niccolo Bolli1,6, Peter Ganly7, Arnold Ganser5, Ultan McDermott1, Konstanze Döhner4, Richard F Schlenk4, Hartmut Döhner4, Peter J Campbell1,8.
Abstract
Underpinning the vision of precision medicine is the concept that causative mutations in a patient's cancer drive its biology and, by extension, its clinical features and treatment response. However, considerable between-patient heterogeneity in driver mutations complicates evidence-based personalization of cancer care. Here, by reanalyzing data from 1,540 patients with acute myeloid leukemia (AML), we explore how large knowledge banks of matched genomic-clinical data can support clinical decision-making. Inclusive, multistage statistical models accurately predicted likelihoods of remission, relapse and mortality, which were validated using data from independent patients in The Cancer Genome Atlas. Comparison of long-term survival probabilities under different treatments enables therapeutic decision support, which is available in exploratory form online. Personally tailored management decisions could reduce the number of hematopoietic cell transplants in patients with AML by 20-25% while maintaining overall survival rates. Power calculations show that databases require information from thousands of patients for accurate decision support. Knowledge banks facilitate personally tailored therapeutic decisions but require sustainable updating, inclusive cohorts and large sample sizes.Entities:
Mesh:
Year: 2017 PMID: 28092685 PMCID: PMC5764082 DOI: 10.1038/ng.3756
Source DB: PubMed Journal: Nat Genet ISSN: 1061-4036 Impact factor: 38.330