Evidence map›Paper›PMID 30721268›Full record

ArticlePloS one2019

The Apparent Diffusion Coefficient (ADC) is a useful biomarker in predicting metastatic colon cancer using the ADC-value of the primary tumor.

Elias Nerad, Andrea Delli Pizzi, Doenja M J Lambregts, Monique Maas, Sharan Wadhwani, Frans C H Bakers, Harrie C M van den Bosch, Regina G H Beets-Tan, Max J Lahaye

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.0field-weighted citation impact, top 12% of its field
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

23 citing papers in PubMed, 38 citations in OpenAlex.

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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

9 authors at 6 institutions in 3 countries.

Elias NeradUniversity of Maastricht and GROW School of Oncology and Developmental Biology, Maastricht, The Netherlands.ORCID 0000-0002-2333-9600
Andrea Delli PizziInstitute for Advanced Biomedical Technology (ITAB), Gabriele d'Annunzio University, Chieti, Italy.ORCID 0000-0002-2011-3753
Doenja M J LambregtsDepartment of Radiology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
Monique MaasDepartment of Radiology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
Sharan WadhwaniDepartment of radiology, Queen Elizabeth Hospital, University Birmingham Hospitals NHS trust, Birmingham, United Kingdom.
Frans C H BakersDepartment of Radiology, Maastricht University Medical Centre, Maastricht, The Netherlands.ORCID 0000-0002-2327-4712
Harrie C M van den BoschDepartment of Radiology, Catharina Hospital, Eindhoven, The Netherlands.
Regina G H Beets-TanUniversity of Maastricht and GROW School of Oncology and Developmental Biology, Maastricht, The Netherlands.
Max J LahayeDepartment of Radiology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
The Netherlands Cancer Institute · NLCambridge University Hospitals NHS Foundation Trust · GBMaastricht University Medical Centre · NLQueen Elizabeth Hospital Birmingham · GBRadboud University Nijmegen · NLUniversity of Chieti-Pescara · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo investigate the role of the apparent diffusion coefficient (ADC) as a potential imaging biomarker to predict metastasis (lymph node metastasis and distant metastasis) in colon cancer based on the ADC-value of the primary tumor.

methodsThirty patients (21M, 9F) were included retrospectively. All patients received a 1.5T MRI of the colon including T2 and DWI sequences. ADC maps were calculated for each patient. An expert reader manually delineated all colon tumors to measure mean ADC and histogram metrics (mean, min, max, median, standard deviation (SD), skewness, kurtosis, 5th-95th percentiles) were calculated. Advanced colon cancer was defined as lymph node mestastasis (N+) or distant metastasis (M+). The student Mann Whitney U-test was used to assess the differences between the ADC means of early and advanced colon cancer. To compare the accuracy of lymph node metastasis (N+) prediction based on morpholigical criteria versus ADC-value of the primary tumor, two blinded readers, determined the lymph node metastasis (N0 vs N+) based on morphological criteria. The sensitivity and specificity in predicting lymph node metastasis was calculated for both readers and for the ADC-value of the primary tumor, with histopathology results as the gold standard.

resultsThere was a significant difference between the mean ADC-value of advanced versus early tumors (p = 0.002). The optimal cut off value was 1179 * 10-3 mm2/s with an area under the curve (AUC) of 0.83 and a sensitivity and specificity of 81% and 86% respectively to predict advanced tumors. Histogram analyses did not add any significant additional value. The sensitivity and specificity for the prediction of lymph node metastasis based on morphological criteria were 40% and 63% for reader 1 and 30% and 88% for reader 2 respectively. The primary tumor ADC-value using 1.179 * 10-3 mm2/s as threshold had a 100% sensitivity and specificity in predicting lymph node metastasis.

conclusionThe ADC-value of the primary tumor has the potential to predict advanced colon cancer, defined as lymph node metastasis or distant metastasis, with lower ADC values significantly associated with advanced tumors. Furthermore the ADC-value of the primary tumor increases the prediction accuracy of lymph node metastasis compared with morphological criteria.

Indexed as

Biomarkers, TumorDiffusion Magnetic Resonance ImagingAgedAged, 80 and overColonic NeoplasmsFemaleHumansLymphatic MetastasisMaleMiddle AgedPredictive Value of TestsRetrospective StudiesBiomarkers, Tumor

Identifiers

PMID30721268
PMCPMC6363286
OpenAlexW2911920471

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.