Evidence map›Paper›PMID 41251848›Full record

ArticleDiscover oncology2025

Development and validation of an AI-augmented deep learning model for survival prediction in de novo metastatic colorectal cancer.

Merih Yalçıner, Efe Cem Erdat, Engin Eren Kavak, Güngör Utkan

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Article in Discover oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

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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

4 authors.

Merih YalçınerMedical Oncology Department, Cebeci Hospital, Ankara University Faculty of Medicine, Dikimevi, Ankara, 06590, Turkey. merihyalciner@gmail.com.ORCID http://orcid.org/0000-0003-3337-2188
Efe Cem ErdatMedical Oncology Department, Cebeci Hospital, Ankara University Faculty of Medicine, Dikimevi, Ankara, 06590, Turkey.ORCID http://orcid.org/0000-0002-1250-1297
Engin Eren KavakAnkara Etlik City Hospital, Medical Oncology Department, Ankara, Turkey.ORCID http://orcid.org/0000-0003-3247-5361
Güngör UtkanMedical Oncology Department, Cebeci Hospital, Ankara University Faculty of Medicine, Dikimevi, Ankara, 06590, Turkey.ORCID http://orcid.org/0000-0001-8445-6993

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeAccurate prognostication in metastatic colorectal cancer (mCRC) remains challenging due to disease heterogeneity. This study aimed to develop and validate an artificial intelligence-augmented deep learning model for risk stratification in patients receiving first-line treatment. METHODS/PATIENTS: We developed a deep neural network with artificial intelligence augmentation, using data from patients with de novo mCRC treated at two major reference centers between 2010 and 2024. Patients with BRAF-mutated and MSI-high tumors were excluded. The model incorporated clinical characteristics, laboratory parameters, and treatment data. The primary outcome was progression-free survival (PFS).

resultsA total of 214 patients were included in the study, with 127 patients in the training and internal validation cohort and 87 patients in the external validation cohort. The model stratified patients into three distinct risk groups with significantly different PFS (log-rank p < 0.001). The low-risk group (n = 34) achieved a median PFS of 16.8 months with a 29% event rate, the medium-risk group (n = 33) showed a median PFS of 9.3 months with a 58% event rate, and the high-risk group (n = 34) demonstrated a median PFS of 7.5 months with a 76% event rate. Feature importance analysis identified carcinoembryonic antigen, neutrophil/lymphocyte ratio, and liver function tests as the strongest predictors of PFS. The model’s performance was consistent across both internal and external validation cohorts.

conclusionsThis deep learning model demonstrates robust prognostic capabilities in mCRC, effectively stratifying patients into distinct risk groups. The model could aid in clinical decision-making and treatment planning for patients receiving first-line therapy.

Indexed as

Artificial intelligenceColorectal cancerMachine learningPrognosis

Identifiers

PMID41251848
PMCPMC12627317

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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.