Evidence map›Paper›PMID 38067353›Full record

ArticleCancers2023

Identifying Genetic Mutation Status in Patients with Colorectal Cancer Liver Metastases Using Radiomics-Based Machine-Learning Models.

Nina Wesdorp, Michiel Zeeuw, Delanie van der Meulen, Iris van 't Erve, Zuhir Bodalal, Joran Roor, Jan Hein van Waesberghe, Shira Moos, Janneke van den Bergh, Irene Nota and 11 more

Registry-linked trialAbstract 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. It is linked to trial NCT02162563 (Treatment Strategies in Colorectal Cancer Patients With Initially Unresectable Liver-only Metastases CAIRO5 a Randomized Phase 3 Study of the Dutch Colorectal Cancer Group), which is not on this map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
–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.

NCT02162563 phase3completednot on this map

Treatment Strategies in Colorectal Cancer Patients With Initially Unresectable Liver-only Metastases CAIRO5 a Randomized Phase 3 Study of the Dutch Colorectal Cancer Group (DCCG)

TypeinterventionalSponsorDutch Colorectal Cancer GroupRan2014 to 2025Enrolled530ConditionsColorectal Cancer, Liver MetastasesArmsFOLFOX/ FOLFIRI with bevacizumab, FOLFOXIRI with bevacizumab, FOLFOX/ FOLFIRI with panitumumab
3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. 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

21 authors.

Nina WesdorpDepartment of Surgery, Amsterdam UMC, Vrije Universiteit Amsterdam, 1081 HV Amsterdam, The Netherlands.
Michiel ZeeuwDepartment of Surgery, Amsterdam UMC, Vrije Universiteit Amsterdam, 1081 HV Amsterdam, The Netherlands.ORCID 0000-0001-7918-5404
Delanie van der MeulenDepartment of Surgery, Amsterdam UMC, Vrije Universiteit Amsterdam, 1081 HV Amsterdam, The Netherlands.ORCID 0000-0002-1678-2057
Iris van 't ErveDepartment of Pathology, The Netherlands Cancer Institute, 1066 CX Amsterdam, The Netherlands.ORCID 0000-0003-3667-9185
Zuhir BodalalDepartment of Radiology, The Netherlands Cancer Institute, 1066 CX Amsterdam, The Netherlands.
Joran RoorDepartment of Health, SAS Institute B.V., 1272 PC Huizen, The Netherlands.
Jan Hein van WaesbergheCancer Center Amsterdam, 1081 HV Amsterdam, The Netherlands.
Shira MoosCancer Center Amsterdam, 1081 HV Amsterdam, The Netherlands.
Janneke van den BerghCancer Center Amsterdam, 1081 HV Amsterdam, The Netherlands.
Irene NotaCancer Center Amsterdam, 1081 HV Amsterdam, The Netherlands.
Susan van DierenCancer Center Amsterdam, 1081 HV Amsterdam, The Netherlands.ORCID 0000-0002-3084-0495
Jaap StokerCancer Center Amsterdam, 1081 HV Amsterdam, The Netherlands.ORCID 0000-0002-9822-3784
Gerrit MeijerDepartment of Pathology, The Netherlands Cancer Institute, 1066 CX Amsterdam, The Netherlands.
Rutger-Jan SwijnenburgCancer Center Amsterdam, 1081 HV Amsterdam, The Netherlands.
Cornelis PuntDepartment of Medical Oncology, Amsterdam UMC, University of Amsterdam, 1105 AZ Amsterdam, The Netherlands.
Joost HuiskensDepartment of Surgery, Amsterdam UMC, Vrije Universiteit Amsterdam, 1081 HV Amsterdam, The Netherlands.
Regina Beets-TanDepartment of Radiology, The Netherlands Cancer Institute, 1066 CX Amsterdam, The Netherlands.
Remond FijnemanDepartment of Pathology, The Netherlands Cancer Institute, 1066 CX Amsterdam, The Netherlands.ORCID 0000-0003-2076-5521
Henk MarqueringCancer Center Amsterdam, 1081 HV Amsterdam, The Netherlands.
Geert KazemierDepartment of Surgery, Amsterdam UMC, Vrije Universiteit Amsterdam, 1081 HV Amsterdam, The Netherlands.
On Behalf Of The Dutch Colorectal Cancer Group Liver Expert Panel

Funding

Dutch Cancer Society 14002/2021-2KWF project 10438
6 · The paper itself

Abstract

For patients with colorectal cancer liver metastases (CRLM), the genetic mutation status is important in treatment selection and prognostication for survival outcomes. This study aims to investigate the relationship between radiomics imaging features and the genetic mutation status (KRAS mutation versus no mutation) in a large multicenter dataset of patients with CRLM and validate these findings in an external dataset. Patients with initially unresectable CRLM treated with systemic therapy of the randomized controlled CAIRO5 trial (NCT02162563) were included. All CRLM were semi-automatically segmented in pre-treatment CT scans and radiomics features were calculated from these segmentations. Additionally, data from the Netherlands Cancer Institute (NKI) were used for external validation. A total of 255 patients from the CAIRO5 trial were included. Random Forest, Gradient Boosting, Gradient Boosting + LightGBM, and Ensemble machine-learning classifiers showed AUC scores of 0.77 (95%CI 0.62-0.92), 0.77 (95%CI 0.64-0.90), 0.72 (95%CI 0.57-0.87), and 0.86 (95%CI 0.76-0.95) in the internal test set. Validation of the models on the external dataset with 129 patients resulted in AUC scores of 0.47-0.56. Machine-learning models incorporating CT imaging features could identify the genetic mutation status in patients with CRLM with a good accuracy in the internal test set. However, in the external validation set, the models performed poorly. External validation of machine-learning models is crucial for the assessment of clinical applicability and should be mandatory in all future studies in the field of radiomics.

Indexed as

colorectal cancerCT scangenetic mutationKRAS mutationliver metastasesradiomics

Identifiers

PMID38067353
PMCPMC10705206

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Registered trials

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.