Evidence map›Paper›PMID 40577661›Full record

ArticleJCO clinical cancer informatics2025

Deep Learning Model for Natural Language to Assess Effectiveness of Patients With Non-Muscle Invasive Bladder Cancer Receiving Intravesical Bacillus Calmette-Guérin Therapy.

Makito Miyake, Naohiro Yonemoto, Kanae Togo, Linghua Xu, Tomoyo Oguri, Masayuki Tanaka, Yoshiyuki Hasegawa, Yoshinobu Izawa, Kenji Araki

Abstract read
In one paragraph

Article in JCO clinical cancer informatics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

9 authors.

Makito MiyakeDepartment of Urology, Nara Medical University, Kashihara, Nara, Japan.ORCID 0000-0001-9503-7356
Naohiro YonemotoDepartment of Biostatistics, Faculty of Medicine, University of Toyama. Toyama-shi, Toyama, Japan.ORCID 0000-0003-3637-2095
Kanae TogoAccess & Value, Pfizer Japan Inc, Shibuya-ku, Tokyo, Japan.ORCID 0000-0003-3964-4009
Linghua XuAccess & Value, Pfizer Japan Inc, Shibuya-ku, Tokyo, Japan.ORCID 0000-0003-0466-5993
Tomoyo OguriOncology Medical Affairs, Pfizer Japan Inc, Shibuya-ku, Tokyo, Japan.ORCID 0000-0002-7655-1517
Masayuki TanakaOncology Medical Affairs, Pfizer Japan Inc, Shibuya-ku, Tokyo, Japan.ORCID 0000-0002-7778-6844
Yoshiyuki HasegawaSystem Integration Sector, NTT DATA Corporation, Koto-ku, Tokyo, Japan.ORCID 0000-0002-2105-3975
Yoshinobu IzawaSystem Integration Sector, NTT DATA Corporation, Koto-ku, Tokyo, Japan.
Kenji ArakiFaculty of Medicine, University of Miyazaki Hospital, Miyazaki-shi, Miyazaki, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeCollecting information on clinical outcomes (recurrence/progression) from complex treatment courses in non-muscle invasive bladder cancer (NMIBC) is challenging and time-consuming. We developed a deep learning natural language processing model to assess outcomes in patients with NMIBC using vast data from electronic health records (EHRs).

methodsThis retrospective study analyzed data from Japanese adults with NMIBC who started Bacillus Calmette-Guérin (BCG) induction therapy between April 2016 and June 2022. A Bidirectional Encoder Representations from Transformers (BERT) model was trained to classify outcomes, supported by human review for past history records. The model's performance was assessed by precision, recall, and F1 scores. We compared the effectiveness of BCG therapy between completion (patients who completed therapy) and non-completion groups.

resultsOf 372 patients studied, 79.3% and 20.7% were in the completion group and the non-completion group, respectively. The final BERT model achieved average F1 scores of 0.91 and 0.98 for time to recurrence (TTR), and 0.74 and 0.94 for time to progression (TTP) before and after human support, respectively. The hazard ratio for TTR in BCG completion versus non-completion groups was 0.40 (95% CI, 0.26 to 0.62) by a multivariate Cox proportional hazard model and 0.41 (95% CI, 0.26 to 0.63) by inverse probability of treatment weighting.

conclusionThe developed model could compare the clinical outcomes between treatments in patients with NMIBC using EHRs. Human support, although required, was needed in only 10% documents and was deemed feasible. The model was able to demonstrate the difference in TTR and TTP between BCG completion and non-completion groups.

Indexed as

BCG VaccineDeep LearningNatural Language ProcessingUrinary Bladder NeoplasmsAdjuvants, ImmunologicAdministration, IntravesicalAgedAged, 80 and overElectronic Health RecordsFemaleHumansMaleMiddle AgedNeoplasm Recurrence, LocalNon-Muscle Invasive Bladder NeoplasmsRetrospective StudiesAdjuvants, ImmunologicBCG Vaccine

Identifiers

PMID40577661
PMCPMC12233173

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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.