Predicting the germline dependence of hematuria risk in prostate cancer radiotherapy patients.


Journal

Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology
ISSN: 1879-0887
Titre abrégé: Radiother Oncol
Pays: Ireland
ID NLM: 8407192

Informations de publication

Date de publication:
08 2023
Historique:
received: 24 12 2022
revised: 09 05 2023
accepted: 17 05 2023
pmc-release: 01 08 2024
medline: 17 7 2023
pubmed: 28 5 2023
entrez: 27 5 2023
Statut: ppublish

Résumé

Late radiation-induced hematuria can develop in prostate cancer patients undergoing radiotherapy and can negatively impact the quality-of-life of survivors. If a genetic component of risk could be modeled, this could potentially be the basis for modifying treatment for high-risk patients. We therefore investigated whether a previously developed machine learning-based modeling method using genome-wide common single nucleotide polymorphisms (SNPs) can stratify patients in terms of the risk of radiation-induced hematuria. We applied a two-step machine learning algorithm that we previously developed for genome-wide association studies called pre-conditioned random forest regression (PRFR). PRFR includes a pre-conditioning step, producing adjusted outcomes, followed by random forest regression modeling. Data was from germline genome-wide SNPs for 668 prostate cancer patients treated with radiotherapy. The cohort was stratified only once, at the outset of the modeling process, into two groups: a training set (2/3 of samples) for modeling and a validation set (1/3 of samples). Post-modeling bioinformatics analysis was conducted to identify biological correlates plausibly associated with the risk of hematuria. The PRFR method achieved significantly better predictive performance compared to other alternative methods (all p < 0.05). The odds ratio between the high and low risk groups, each of which consisted of 1/3 of samples in the validation set, was 2.87 (p = 0.029), implying a clinically useful level of discrimination. Bioinformatics analysis identified six key proteins encoded by CTNND2, GSK3B, KCNQ2, NEDD4L, PRKAA1, and TXNL1 genes as well as four statistically significant biological process networks previously shown to be associated with the bladder and urinary tract. The risk of hematuria is significantly dependent on common genetic variants. The PRFR algorithm resulted in a stratification of prostate cancer patients at differential risk levels of post-radiotherapy hematuria. Bioinformatics analysis identified important biological processes involved in radiation-induced hematuria.

Sections du résumé

BACKGROUND AND PURPOSE
Late radiation-induced hematuria can develop in prostate cancer patients undergoing radiotherapy and can negatively impact the quality-of-life of survivors. If a genetic component of risk could be modeled, this could potentially be the basis for modifying treatment for high-risk patients. We therefore investigated whether a previously developed machine learning-based modeling method using genome-wide common single nucleotide polymorphisms (SNPs) can stratify patients in terms of the risk of radiation-induced hematuria.
MATERIALS AND METHODS
We applied a two-step machine learning algorithm that we previously developed for genome-wide association studies called pre-conditioned random forest regression (PRFR). PRFR includes a pre-conditioning step, producing adjusted outcomes, followed by random forest regression modeling. Data was from germline genome-wide SNPs for 668 prostate cancer patients treated with radiotherapy. The cohort was stratified only once, at the outset of the modeling process, into two groups: a training set (2/3 of samples) for modeling and a validation set (1/3 of samples). Post-modeling bioinformatics analysis was conducted to identify biological correlates plausibly associated with the risk of hematuria.
RESULTS
The PRFR method achieved significantly better predictive performance compared to other alternative methods (all p < 0.05). The odds ratio between the high and low risk groups, each of which consisted of 1/3 of samples in the validation set, was 2.87 (p = 0.029), implying a clinically useful level of discrimination. Bioinformatics analysis identified six key proteins encoded by CTNND2, GSK3B, KCNQ2, NEDD4L, PRKAA1, and TXNL1 genes as well as four statistically significant biological process networks previously shown to be associated with the bladder and urinary tract.
CONCLUSION
The risk of hematuria is significantly dependent on common genetic variants. The PRFR algorithm resulted in a stratification of prostate cancer patients at differential risk levels of post-radiotherapy hematuria. Bioinformatics analysis identified important biological processes involved in radiation-induced hematuria.

Identifiants

pubmed: 37244355
pii: S0167-8140(23)00261-X
doi: 10.1016/j.radonc.2023.109723
pmc: PMC10524941
mid: NIHMS1904162
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

109723

Subventions

Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States
Organisme : NIA NIH HHS
ID : R01 AG048769
Pays : United States
Organisme : NCI NIH HHS
ID : R21 CA234752
Pays : United States

Informations de copyright

Copyright © 2023 The Author(s). Published by Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Références

Int J Mol Sci. 2019 May 29;20(11):
pubmed: 31146414
Proc Natl Acad Sci U S A. 2009 Aug 4;106(31):12838-42
pubmed: 19625618
Curr Opin Nephrol Hypertens. 2012 Sep;21(5):541-6
pubmed: 22691876
BJU Int. 2019 Apr;123(4):585-594
pubmed: 30113758
Genet Epidemiol. 2011 Nov;35(7):597-605
pubmed: 21769935
Cancer Lett. 2016 Nov 1;382(1):95-109
pubmed: 26944314
DNA Cell Biol. 2012 Nov;31(11):1604-9
pubmed: 22994212
Prostate. 2009 Mar 1;69(4):411-8
pubmed: 19116988
Ann Intern Med. 2016 Apr 5;164(7):488-97
pubmed: 26810935
Sci Rep. 2017 Feb 24;7:43381
pubmed: 28233873
Radiother Oncol. 2022 Mar;168:75-82
pubmed: 35077710
Semin Radiat Oncol. 2017 Oct;27(4):300-309
pubmed: 28865512
PLoS One. 2020 Feb 27;15(2):e0226157
pubmed: 32106268
BJU Int. 2013 Jun;111(8):E319-24
pubmed: 23360671
Nat Genet. 2016 Oct;48(10):1284-1287
pubmed: 27571263
Am J Pathol. 2004 Jul;165(1):63-9
pubmed: 15215162
Urology. 2008 Nov;72(5):1130-4
pubmed: 18400265
Gigascience. 2015 Feb 25;4:7
pubmed: 25722852
Urology. 2019 Sep;131:190-195
pubmed: 31201826
JNCI Cancer Spectr. 2020 May 11;4(5):pkaa039
pubmed: 33490863
Mol Cancer. 2009 Mar 10;8:19
pubmed: 19284555
Int J Radiat Oncol Biol Phys. 2018 May 1;101(1):128-135
pubmed: 29502932
Front Oncol. 2018 Oct 12;8:450
pubmed: 30370253
Gigascience. 2021 Feb 16;10(2):
pubmed: 33590861
Investig Clin Urol. 2022 Jan;63(1):42-52
pubmed: 34983122
Sci Rep. 2016 Jan 25;6:19708
pubmed: 26806558
F1000Res. 2017 Feb 1;6:97
pubmed: 28620455
Ann Intern Med. 2015 Jan 6;162(1):W1-73
pubmed: 25560730
Genome Res. 2002 Jun;12(6):996-1006
pubmed: 12045153
Rev Urol. 2004;6 Suppl 3:S19-28
pubmed: 16985861
Hypertension. 2009 Oct;54(4):796-801
pubmed: 19635985
Cancer Discov. 2014 Feb;4(2):155-65
pubmed: 24441285
Case Rep Urol. 2015;2015:134651
pubmed: 26491598
Radiat Oncol. 2015 Feb 19;10:44
pubmed: 25890265
Clin Cancer Res. 2010 Nov 1;16(21):5124-32
pubmed: 20889919
Am J Clin Oncol. 2015 Jun;38(3):331-6
pubmed: 24322335
Nat Rev Neurosci. 2008 Jun;9(6):453-66
pubmed: 18490916
J Natl Cancer Inst. 2020 Feb 1;112(2):179-190
pubmed: 31095341
Int J Radiat Oncol Biol Phys. 2010 Mar 1;76(3 Suppl):S116-22
pubmed: 20171505
Front Cell Dev Biol. 2019 Jun 27;7:111
pubmed: 31316980
Am J Clin Exp Urol. 2019 Jun 15;7(3):110-122
pubmed: 31317051
World J Urol. 2011 Apr;29(2):211-6
pubmed: 20577744
J Urol. 2013 Jul;190(1):102-8
pubmed: 23376709

Auteurs

Jung Hun Oh (JH)

Department of Medical Physics, Memorial Sloan Kettering Cancer Center, New York, NY, United States. Electronic address: ohj@mskcc.org.

Sangkyu Lee (S)

Department of Medical Physics, Memorial Sloan Kettering Cancer Center, New York, NY, United States.

Maria Thor (M)

Department of Medical Physics, Memorial Sloan Kettering Cancer Center, New York, NY, United States.

Barry S Rosenstein (BS)

Department of Radiation Oncology, Icahn School of Medicine at Mount Sinai, New York, NY, United States.

Allen Tannenbaum (A)

Departments of Computer Science and Applied Mathematics & Statistics, Stony Brook University, Stony Brook, NY, United States.

Sarah Kerns (S)

Department of Radiation Oncology, Medical College of Wisconsin, Milwaukee, WI, United States.

Joseph O Deasy (JO)

Department of Medical Physics, Memorial Sloan Kettering Cancer Center, New York, NY, United States.

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Classifications MeSH