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.

Precision oncology for acute myeloid leukemia using a knowledge bank approach / M. Gerstung, E. Papaemmanuil, I. Martincorena, L. Bullinger, V.I. Gaidzik, P. Paschka, M. Heuser, F. Thol, N. Bolli, P. Ganly, A. Ganser, U. Mcdermott, K. Döhner, R.F. Schlenk, H. Döhner, P.J. Campbell. - In: NATURE GENETICS. - ISSN 1061-4036. - 49:3(2017), pp. 332-340. [10.1038/ng.3756]

Precision oncology for acute myeloid leukemia using a knowledge bank approach

N. Bolli;
2017

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.
English
Genetics
Settore MED/15 - Malattie del Sangue
Articolo
Esperti anonimi
Pubblicazione scientifica
2017
Nature Publishing Group
49
3
332
340
9
Pubblicato
Periodico con rilevanza internazionale
scopus
crossref
pubmed
Aderisco
info:eu-repo/semantics/article
Precision oncology for acute myeloid leukemia using a knowledge bank approach / M. Gerstung, E. Papaemmanuil, I. Martincorena, L. Bullinger, V.I. Gaidzik, P. Paschka, M. Heuser, F. Thol, N. Bolli, P. Ganly, A. Ganser, U. Mcdermott, K. Döhner, R.F. Schlenk, H. Döhner, P.J. Campbell. - In: NATURE GENETICS. - ISSN 1061-4036. - 49:3(2017), pp. 332-340. [10.1038/ng.3756]
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Prodotti della ricerca::01 - Articolo su periodico
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262
Article (author)
no
M. Gerstung, E. Papaemmanuil, I. Martincorena, L. Bullinger, V.I. Gaidzik, P. Paschka, M. Heuser, F. Thol, N. Bolli, P. Ganly, A. Ganser, U. Mcdermott, K. Döhner, R.F. Schlenk, H. Döhner, P.J. Campbell
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/474183
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