Evidence map›Paper›PMID 41832931›Full record

ArticleEuropean radiology2026

Can ADC differentiate cellular from acellular mucin in mucinous adenocarcinoma tumor beds after treatment of rectal cancer? A multicenter study.

Maria El Homsi, Yousef Mazaheri, Jonathan Kuten, Onur Yildirim, Marina Corines, Natally Horvat, Akshay Baheti, Shannon P Sheedy, Sonia Lee, Stephanie Nougaret and 6 more

Abstract readMulticenter Study
PubMed Publisher
In one paragraph

Article in European radiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

16 authors.

Maria El Homsi *Department of Radiology, Memorial Sloan Kettering Cancer Center, New York, NY, USA. elhomsim@mskcc.org.ORCID http://orcid.org/0000-0002-8483-3653
Yousef Mazaheri *Department of Physics, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Jonathan KutenDepartment of Radiology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Onur YildirimDepartment of Radiology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Marina CorinesDepartment of Radiology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Natally HorvatDepartment of Radiology, Mayo Clinic, Rochester, MN, USA.
Akshay BahetiDepartment of Radiodiagnosis, Tata Memorial Centre, Homi Bhabha National Institute, Mumbai, India.
Shannon P SheedyDepartment of Radiology, Mayo Clinic, Rochester, MN, USA.
Sonia LeeDepartment of Radiological Sciences, Irvine Medical Center, University of California, Orange, CA, USA.
Stephanie NougaretDepartment of Radiology, Montpellier Cancer Research Institute, Montpellier, France.
Randy ErnstDepartment of Radiology, University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Courtney MorenoDepartment of Radiology and Imaging Sciences, Emory University School of Medicine, Atlanta, GA, USA.
Elena KorngoldDepartment of Radiology, Oregon Health and Science University, Portland, OR, USA.
Stephanie LobaughDepartment of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Marinela CapanuDepartment of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Marc GollubDepartment of Radiology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesTo determine if the apparent diffusion coefficient (ADC) can distinguish acellular mucin from cellular mucin in the treated tumor bed of patients with mucinous rectal adenocarcinoma after neoadjuvant therapy. MATERIALS AND

methodsThis retrospective study included patients with mucinous rectal adenocarcinoma treated with neoadjuvant therapy, followed by restaging MRI and surgical resection or biopsy. Three radiologists blinded to histopathology results independently segmented volumes of interest on diffusion-weighted imaging and ADC maps. A medical physicist performed histogram analysis of ADC map segmentations, calculating various ADC metrics: mean, standard deviation, median, 1st quartile, 2nd quartile, 3rd quartile, and 4th quartile. The Wilcoxon rank sum test with false discovery rate correction for multiple testing was used to examine associations between ADC metrics and tumor mucin cellularity at histopathology for each reader. Multivariable logistic regression was used to adjust for acquisition parameters and institutions.

resultsOf 150 patients (mean age, 58 ± 14 years; 48/150 (32% female), 25 patients (17%) had acellular mucin and 125 (83%) had cellular mucin at histopathology. At univariable analysis, there was no significant association between any ADC metric and tumor mucin cellularity (q-value = 0.14-0.58). At multivariable analysis, most ADC metrics were significantly associated with tumor mucin cellularity for all readers (q-values = 0.016-0.025) with odds ratios between 0.09 (95% CI: 0.02, 0.42) and 0.49 (95% CI: 0.22, 0.96).

conclusionsADC may be a potential tool for assessing pathologic complete response in mucinous rectal adenocarcinoma after neoadjuvant treatment, after adjusting for acquisition parameters and institutions. KEY POINTS: QuestionCan the apparent diffusion coefficient (ADC) distinguish between cellular and acellular mucin (i.e., pathologic complete response) in mucinous rectal adenocarcinoma after neoadjuvant therapy? FindingsAfter controlling for acquisition parameters, ADC metrics were significantly associated with tumor mucin cellularity. Clinical relevanceAcellular mucin is equivalent to clinical complete response and can undergo watch-and-wait management, whereas cellular mucin is incomplete response, and its safety for watch-and-wait management is not validated. ADC may be a potential tool to make the distinction to assist treatment decision-making.

Indexed as

Adenocarcinoma, MucinousDiffusion Magnetic Resonance ImagingMucinsRectal NeoplasmsAdultAgedFemaleHumansMaleMiddle AgedNeoadjuvant TherapyRetrospective StudiesTreatment OutcomeMucinsApparent diffusion coefficientMucinous rectal cancerPathologic complete response

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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.