Risk Prediction Using Bayesian Networks: An Immunotherapy Case Study in Patients With Metastatic Renal Cell Carcinoma.


Journal

JCO clinical cancer informatics
ISSN: 2473-4276
Titre abrégé: JCO Clin Cancer Inform
Pays: United States
ID NLM: 101708809

Informations de publication

Date de publication:
03 2021
Historique:
entrez: 25 3 2021
pubmed: 26 3 2021
medline: 1 9 2021
Statut: ppublish

Résumé

To address the need for more accurate risk stratification models for cancer immuno-oncology, this study aimed to develop a machine-learned Bayesian network model (BNM) for predicting outcomes in patients with metastatic renal cell carcinoma (mRCC) being treated with immunotherapy. Patient-level data from the randomized, phase III CheckMate 025 clinical trial comparing nivolumab with everolimus for second-line treatment in patients with mRCC were used to develop the BNM. Outcomes of interest were overall survival (OS), all-cause adverse events, and treatment-related adverse events (TRAE) over 36 months after treatment initiation. External validation of the model's predictions for OS was conducted using data from select centers from the International Metastatic Renal Cell Carcinoma Database Consortium (IMDC). Areas under the receiver operating characteristic curve (AUCs) for BNM-based classification of OS using baseline data were 0.74, 0.71, and 0.68 over months 12, 24, and 36, respectively. AUC for OS at 12 months increased to 0.86 when treatment response and progression status in year 1 were included as predictors; progression and response at 12 months were highly prognostic of all outcomes over the 36-month period. AUCs for adverse events and treatment-related adverse events were approximately 0.6 at 12 months but increased to approximately 0.7 by 36 months. Sensitivity analysis comparing the BNM with machine learning classifiers showed comparable performance. Test AUC on IMDC data for 12-month OS was 0.71 despite several variable imbalances. Notably, the BNM outperformed the IMDC risk score alone. The validated BNM performed well at prediction using baseline data, particularly with the inclusion of response and progression at 12 months. Additionally, the results suggest that 12 months of follow-up data alone may be sufficient to inform long-term survival projections in patients with mRCC.

Identifiants

pubmed: 33764818
doi: 10.1200/CCI.20.00107
pmc: PMC8140790
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

326-337

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Auteurs

Alind Gupta (A)

Cytel, Toronto, Ontario, Canada.

Paul Arora (P)

Cytel, Toronto, Ontario, Canada.
University of Toronto, Toronto, Ontario, Canada.

Darren Brenner (D)

University of Calgary, Calgary, Alberta, Canada.

Jacqueline Vanderpuye-Orgle (J)

Parexel, Billerica, MA.

Devon J Boyne (DJ)

University of Calgary, Calgary, Alberta, Canada.

Mark Edmondson-Jones (M)

Parexel, London, United Kingdom.

Elena Parkhomenko (E)

Parexel, London, United Kingdom.

Warren Stevens (W)

Parexel, London, United Kingdom.

Shaan Dudani (S)

University of Calgary, Calgary, Alberta, Canada.

Daniel Y C Heng (DYC)

University of Calgary, Calgary, Alberta, Canada.

Samuel Wagner (S)

Bristol Myers Squibb, Princeton, NJ.

John Borrill (J)

Bristol Myers Squibb, Uxbridge, United Kingdom.

Elise Wu (E)

Bristol Myers Squibb, Princeton, NJ.

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Classifications MeSH