Evidence map›Paper›PMID 38236635›Full record

ArticleJMIR medical informatics2024

Predicting Depression Risk in Patients With Cancer Using Multimodal Data: Algorithm Development Study.

Anne de Hond, Marieke van Buchem, Claudio Fanconi, Mohana Roy, Douglas Blayney, Ilse Kant, Ewout Steyerberg, Tina Hernandez-Boussard

Abstract read
In one paragraph

Article in JMIR medical informatics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
–field-weighted citation impact
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

15 citing papers in PubMed.

  1. Review
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  14. Navigating the Intersection of Technology and Depression Precision Medicine.Advances in experimental medicine and biology · 2024
    Review
  15. 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.

Anne de HondClinical AI Implementation and Research Lab, Leiden University Medical Centre, Leiden, Netherlands.ORCID https://orcid.org/0000-0002-3473-3398
Marieke van BuchemClinical AI Implementation and Research Lab, Leiden University Medical Centre, Leiden, Netherlands.ORCID https://orcid.org/0000-0002-2917-0842
Claudio FanconiDepartment of Medicine (Biomedical Informatics), Stanford Medicine, Stanford University, Stanford, CA, United States.ORCID https://orcid.org/0000-0001-5308-3821
Mohana RoyDepartment of Medical Oncology, Stanford Medicine, Stanford University, Stanford, CA, United States.ORCID https://orcid.org/0000-0002-9997-8935
Douglas BlayneyDepartment of Medical Oncology, Stanford Medicine, Stanford University, Stanford, CA, United States.ORCID https://orcid.org/0000-0002-7931-4533
Ilse KantClinical AI Implementation and Research Lab, Leiden University Medical Centre, Leiden, Netherlands.ORCID https://orcid.org/0000-0002-5273-5178
Ewout SteyerbergClinical AI Implementation and Research Lab, Leiden University Medical Centre, Leiden, Netherlands.ORCID https://orcid.org/0000-0002-7787-0122
Tina Hernandez-BoussardDepartment of Medicine (Biomedical Informatics), Stanford Medicine, Stanford University, Stanford, CA, United States.ORCID https://orcid.org/0000-0001-6553-3455

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPatients with cancer starting systemic treatment programs, such as chemotherapy, often develop depression. A prediction model may assist physicians and health care workers in the early identification of these vulnerable patients.

objectiveThis study aimed to develop a prediction model for depression risk within the first month of cancer treatment.

methodsWe included 16,159 patients diagnosed with cancer starting chemo- or radiotherapy treatment between 2008 and 2021. Machine learning models (eg, least absolute shrinkage and selection operator [LASSO] logistic regression) and natural language processing models (Bidirectional Encoder Representations from Transformers [BERT]) were used to develop multimodal prediction models using both electronic health record data and unstructured text (patient emails and clinician notes). Model performance was assessed in an independent test set (n=5387, 33%) using area under the receiver operating characteristic curve (AUROC), calibration curves, and decision curve analysis to assess initial clinical impact use.

resultsAmong 16,159 patients, 437 (2.7%) received a depression diagnosis within the first month of treatment. The LASSO logistic regression models based on the structured data (AUROC 0.74, 95% CI 0.71-0.78) and structured data with email classification scores (AUROC 0.74, 95% CI 0.71-0.78) had the best discriminative performance. The BERT models based on clinician notes and structured data with email classification scores had AUROCs around 0.71. The logistic regression model based on email classification scores alone performed poorly (AUROC 0.54, 95% CI 0.52-0.56), and the model based solely on clinician notes had the worst performance (AUROC 0.50, 95% CI 0.49-0.52). Calibration was good for the logistic regression models, whereas the BERT models produced overly extreme risk estimates even after recalibration. There was a small range of decision thresholds for which the best-performing model showed promising clinical effectiveness use. The risks were underestimated for female and Black patients.

conclusionsThe results demonstrated the potential and limitations of machine learning and multimodal models for predicting depression risk in patients with cancer. Future research is needed to further validate these models, refine the outcome label and predictors related to mental health, and address biases across subgroups.

Indexed as

artificial intelligencecancercancer carecancer treatmentcarechemotherapyclinical decision supportdecision supportdepressiondepression riskdiagnosismachine learningmental healthnatural language processingoncologypatients with cancerprediction modelradiotherapyvalidation

Identifiers

PMID38236635
PMCPMC10835583

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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.