A Machine Learning Decision Support System (DSS) for Neuroendocrine Tumor Patients Treated with Somatostatin Analog (SSA) Therapy.

machine learning neuroendocrine tumors predictive biomarkers prognostic factors random forest classifier somatostatin analogs

Journal

Diagnostics (Basel, Switzerland)
ISSN: 2075-4418
Titre abrégé: Diagnostics (Basel)
Pays: Switzerland
ID NLM: 101658402

Informations de publication

Date de publication:
28 Apr 2021
Historique:
received: 16 03 2021
revised: 23 04 2021
accepted: 26 04 2021
entrez: 30 4 2021
pubmed: 1 5 2021
medline: 1 5 2021
Statut: epublish

Résumé

The application of machine learning (ML) techniques could facilitate the identification of predictive biomarkers of somatostatin analog (SSA) efficacy in patients with neuroendocrine tumors (NETs). We collected data from 74 patients with a pancreatic or gastrointestinal NET who received SSA as first-line therapy. We developed three classification models to predict whether the patient would experience a progressive disease (PD) after 12 or 18 months based on clinic-pathological factors at the baseline. The dataset included 70 samples and 15 features. We initially developed three classification models with accuracy ranging from 55% to 70%. We then compared ten different ML algorithms. In all but one case, the performance of the Multinomial Naïve Bayes algorithm (80%) was the highest. The support vector machine classifier (SVC) had a higher performance for the recall metric of the progression-free outcome (97% vs. 94%). Overall, for the first time, we documented that the factors that mainly influenced progression-free survival (PFS) included age, the number of metastatic sites and the primary site. In addition, the following factors were also isolated as important: adverse events G3-G4, sex, Ki67, metastatic site (liver), functioning NET, the primary site and the stage. In patients with advanced NETs, ML provides a predictive model that could potentially be used to differentiate prognostic groups and to identify patients for whom SSA therapy as a single agent may not be sufficient to achieve a long-lasting PFS.

Identifiants

pubmed: 33925256
pii: diagnostics11050804
doi: 10.3390/diagnostics11050804
pmc: PMC8145352
pii:
doi:

Types de publication

Journal Article

Langues

eng

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Auteurs

Jasminka Hasic Telalovic (J)

Computer Science Department, School of Science and Technology, University Sarajevo, 71210 Sarajevo, Bosnia and Herzegovina.

Serena Pillozzi (S)

Medical Oncology Unit, Careggi University Hospital, Largo Brambilla 4, 50134 Florence, Italy.

Rachele Fabbri (R)

Department of Information Engineering, University of Florence, Via S. Marta 3, 50139 Florence, Italy.

Alice Laffi (A)

Division of Gastrointestinal Medical Oncology and Neuroendocrine Tumors, European Institute of Oncology, IEO, IRCCS, Via Ripamonti 435, 20141 Milan, Italy.

Daniele Lavacchi (D)

Medical Oncology Unit, Careggi University Hospital, Largo Brambilla 4, 50134 Florence, Italy.

Virginia Rossi (V)

Medical Oncology Unit, Careggi University Hospital, Largo Brambilla 4, 50134 Florence, Italy.

Lorenzo Dreoni (L)

Medical Oncology Unit, Careggi University Hospital, Largo Brambilla 4, 50134 Florence, Italy.

Francesca Spada (F)

Division of Gastrointestinal Medical Oncology and Neuroendocrine Tumors, European Institute of Oncology, IEO, IRCCS, Via Ripamonti 435, 20141 Milan, Italy.

Nicola Fazio (N)

Division of Gastrointestinal Medical Oncology and Neuroendocrine Tumors, European Institute of Oncology, IEO, IRCCS, Via Ripamonti 435, 20141 Milan, Italy.

Amedeo Amedei (A)

Department of Experimental and Clinical Medicine, University of Florence, Largo Brambilla 3, 50134 Florence, Italy.

Ernesto Iadanza (E)

Department of Information Engineering, University of Florence, Via S. Marta 3, 50139 Florence, Italy.

Lorenzo Antonuzzo (L)

Medical Oncology Unit, Careggi University Hospital, Largo Brambilla 4, 50134 Florence, Italy.

Classifications MeSH