Evidence map›Paper›PMID 38762636›Full record

ArticleNature communications2024

Histopathologic image-based deep learning classifier for predicting platinum-based treatment responses in high-grade serous ovarian cancer.

Byungsoo Ahn, Damin Moon, Hyun-Soo Kim, Chung Lee, Nam Hoon Cho, Heung-Kook Choi, Dongmin Kim, Jung-Yun Lee, Eun Ji Nam, Dongju Won and 16 more

Abstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing 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

37 citing papers in PubMed.

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  9. The consensus molecular subtypes of esophageal squamous cell carcinoma.Signal transduction and targeted therapy · 2026
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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

26 authors.

Byungsoo Ahn *Department of Pathology, Severance Hospital, Yonsei University College of Medicine, Seoul, South Korea.ORCID http://orcid.org/0009-0007-3641-9590
Damin Moon *Artificial Intelligence Research Center, JLK Inc., Seoul, South Korea.ORCID http://orcid.org/0009-0007-1085-1633
Hyun-Soo Kim *Department of Pathology and Translational Genomics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea.ORCID http://orcid.org/0000-0003-4730-221X
Chung LeeDepartment of Pathology, Severance Hospital, Yonsei University College of Medicine, Seoul, South Korea.
Nam Hoon ChoDepartment of Pathology, Severance Hospital, Yonsei University College of Medicine, Seoul, South Korea.
Heung-Kook ChoiArtificial Intelligence Research Center, JLK Inc., Seoul, South Korea.
Dongmin KimArtificial Intelligence Research Center, JLK Inc., Seoul, South Korea.ORCID http://orcid.org/0000-0003-4121-5035
Jung-Yun LeeDepartment of Obstetrics and Gynecology, Institute of Women's Life Medical Science, Yonsei University College of Medicine, Seoul, South Korea.ORCID http://orcid.org/0000-0003-4094-2097
Eun Ji NamDepartment of Obstetrics and Gynecology, Institute of Women's Life Medical Science, Yonsei University College of Medicine, Seoul, South Korea.
Dongju WonDepartment of Laboratory Medicine, Yonsei University College of Medicine, Seoul, South Korea.
Hee Jung AnDepartment of Pathology, CHA Bundang Medical Center, CHA University School of Medicine, Seongnam, South Korea.
Sun Young KwonDepartment of Pathology, Keimyung University School of Medicine, Daegu, South Korea.
Su-Jin ShinDepartment of Pathology, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, South Korea.
Hye Ra JungDepartment of Pathology, Keimyung University School of Medicine, Daegu, South Korea.
Dohee KwonDepartment of Pathology, Severance Hospital, Yonsei University College of Medicine, Seoul, South Korea.
Heejung ParkDepartment of Pathology, Severance Hospital, Yonsei University College of Medicine, Seoul, South Korea.
Milim KimDepartment of Pathology, Severance Hospital, Yonsei University College of Medicine, Seoul, South Korea.
Yoon Jin ChaDepartment of Pathology, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, South Korea.
Hyunjin ParkDepartment of Pathology, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, South Korea.
Yangkyu LeeDepartment of Pathology, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, South Korea.
Songmi NohDepartment of Diagnostic Pathology, Gangnam CHA Medical Center, CHA University College of Medicine, Seoul, South Korea.
Yong-Moon LeeDepartment of Pathology, Dankook University School of Medicine, Cheonan, South Korea.
Sung-Eun ChoiDepartment of Pathology, CHA Bundang Medical Center, CHA University School of Medicine, Seongnam, South Korea.
Ji Min KimDepartment of Pathology, Ewha Womans University, Seoul, South Korea.
Sun Hee SungDepartment of Pathology, Ewha Womans University, Seoul, South Korea.
Eunhyang ParkDepartment of Pathology, Severance Hospital, Yonsei University College of Medicine, Seoul, South Korea. epark54@yuhs.ac.ORCID http://orcid.org/0000-0003-2658-5054

Funding

PROVIDE RABBITS, RATS MICE, HAMSTERS GERBILS, GUINEA PIGS27307C0012 · NIEHS · PI BOLEN, WAYNE · 2007 to 2007
$1.0M
NIEHS NIH HHS 27307C0012
6 · The paper itself

Abstract

Platinum-based chemotherapy is the cornerstone treatment for female high-grade serous ovarian carcinoma (HGSOC), but choosing an appropriate treatment for patients hinges on their responsiveness to it. Currently, no available biomarkers can promptly predict responses to platinum-based treatment. Therefore, we developed the Pathologic Risk Classifier for HGSOC (PathoRiCH), a histopathologic image-based classifier. PathoRiCH was trained on an in-house cohort (n = 394) and validated on two independent external cohorts (n = 284 and n = 136). The PathoRiCH-predicted favorable and poor response groups show significantly different platinum-free intervals in all three cohorts. Combining PathoRiCH with molecular biomarkers provides an even more powerful tool for the risk stratification of patients. The decisions of PathoRiCH are explained through visualization and a transcriptomic analysis, which bolster the reliability of our model's decisions. PathoRiCH exhibits better predictive performance than current molecular biomarkers. PathoRiCH will provide a solid foundation for developing an innovative tool to transform the current diagnostic pipeline for HGSOC.

Indexed as

Cystadenocarcinoma, SerousDeep LearningOvarian NeoplasmsPlatinumAdultAgedBiomarkers, TumorCohort StudiesFemaleHumansMiddle AgedNeoplasm GradingReproducibility of ResultsTreatment OutcomeBiomarkers, TumorPlatinum

Identifiers

PMID38762636
PMCPMC11102549

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.