Evidence map›Paper›PMID 37686482›Full record

ArticleCancers2023

Predicting Severe Haematological Toxicity in Gastrointestinal Cancer Patients Undergoing 5-FU-Based Chemotherapy: A Bayesian Network Approach.

Oskitz Ruiz Sarrias, Cristina Gónzalez Deza, Javier Rodríguez Rodríguez, Olast Arrizibita Iriarte, Angel Vizcay Atienza, Teresa Zumárraga Lizundia, Onintza Sayar Beristain, Azucena Aldaz Pastor

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
1.3field-weighted citation impact, top 18% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 1 synthesis or guideline pooled it, 5 citations in OpenAlex.

  1. Pooled it
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

Oskitz Ruiz SarriasDepartment of Mathematics and Statistic, NNBi, 31191 Esquiroz, Navarra, Spain.
Cristina Gónzalez DezaDepartment of Medical Oncology, Clínica Universidad De Navarra, 31008 Pamplona, Navarra, Spain.
Javier Rodríguez RodríguezDepartment of Medical Oncology, Clínica Universidad De Navarra, 31008 Pamplona, Navarra, Spain.ORCID 0000-0003-1899-4384
Olast Arrizibita IriarteDepartment of Mathematics and Statistic, NNBi, 31191 Esquiroz, Navarra, Spain.
Angel Vizcay AtienzaDepartment of Medical Oncology, Clínica Universidad De Navarra, 31008 Pamplona, Navarra, Spain.ORCID 0000-0001-9386-3654
Teresa Zumárraga LizundiaDepartment of Medical Oncology, Clínica Universidad De Navarra, 31008 Pamplona, Navarra, Spain.
Onintza Sayar BeristainDepartment of Mathematics and Statistic, NNBi, 31191 Esquiroz, Navarra, Spain.
Azucena Aldaz PastorPharmacy Unit, Clinica Universidad De Navarra, 31008 Pamplona, Navarra, Spain.
Clinica Universidad de Navarra · ES

Funding

Gobierno de Navarra platafoRma de intElIgeNcia artiFicial para la predicción de tOxicidad y Recurrencia del CancEr Referencia: 0011-1411-2020-000074
6 · The paper itself

Abstract

purposeSevere toxicity is reported in about 30% of gastrointestinal cancer patients receiving 5-Fluorouracil (5-FU)-based chemotherapy. To date, limited tools exist to identify at risk patients in this setting. The objective of this study was to address this need by designing a predictive model using a Bayesian network, a probabilistic graphical model offering robust, explainable predictions.

methodsWe utilized a dataset of 267 gastrointestinal cancer patients, conducting preprocessing, and splitting it into TRAIN and TEST sets (80%:20% ratio). The RandomForest algorithm assessed variable importance based on MeanDecreaseGini coefficient. The bnlearn R library helped design a Bayesian network model using a 10-fold cross-validation on the TRAIN set and the aic-cg method for network structure optimization. The model's performance was gauged based on accuracy, sensitivity, and specificity, using cross-validation on the TRAIN set and independent validation on the TEST set.

resultsThe model demonstrated satisfactory performance with an average accuracy of 0.85 (±0.05) and 0.80 on TRAIN and TEST datasets, respectively. The sensitivity and specificity were 0.82 (±0.14) and 0.87 (±0.07) for the TRAIN dataset, and 0.71 and 0.83 for the TEST dataset, respectively. A user-friendly tool was developed for clinical implementation.

conclusionsDespite several limitations, our Bayesian network model demonstrated a high level of accuracy in predicting the risk of developing severe haematological toxicity in gastrointestinal cancer patients receiving 5-FU-based chemotherapy. Future research should aim at model validation in larger cohorts of patients and different clinical settings.

Indexed as

5-FUartificial intelligenceBayesian networkgastrointestinal cancerhaematotoxicity predictionleukopeniamachine learningneutropeniathrombocytopenia

Identifiers

PMID37686482
PMCPMC10486471
OpenAlexW4386074121

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.