Literature DB >> 20081807

Aggressiveness of 'true' interval invasive ductal carcinomas of the breast in postmenopausal women.

Bert van der Vegt1, Jelle Wesseling, Ruud M Pijnappel, Monique D Dorrius, Gerard J den Heeten, Marnix A J de Roos, Geertruida H de Bock.   

Abstract

There is debate whether interval carcinomas differ from screen-detected tumours biologically. In this study, clinico-pathological parameters and the expression of well-validated biological markers were compared between 'true' interval carcinomas and screen-detected/missed carcinomas hypothesising that 'true' interval carcinomas show a more aggressive biological behaviour. The study group consisted of 92 consecutive postmenopausal women attending the breast screening programme and presenting with an invasive ductal carcinoma. All screening mammograms were re-reviewed. Sixteen patients had a 'true' interval carcinoma. Seven carcinomas were missed at screening, but detected on re-reviewing of the screening mammogram. Radiological characteristics were assessed from diagnostic mammograms. Data on patient- and tumour characteristics and follow-up data were recorded from hospital records. Median follow-up was 61 months. Immunohistochemistry for ER, PR, Her2/neu and p53 was performed on TMA sections. Univariate and multivariate logistic regression analyses were performed. In univariate analysis, 'true' interval carcinomas were significantly larger (odd ratios (OR) 7.2, 95% CI 1.8-28.1) and less frequently ER (OR 0.3, 95% CI 0.1-0.9) and PR (OR 0.3, 95% CI 0.1-1.0) positive. In multivariate analysis, 'true' interval carcinoma was independently associated with larger tumours (OR 7.0, 95% CI 1.4-36.2). A trend toward ER negativity was found (OR 0.3, 95% CI 0.1-1.1). 'True' interval carcinomas showed a trend toward a decreased relapse-free survival (HR 1.7 95% CI 0.9-3.1). Although 'true' interval carcinomas were significantly larger than screen-detected/missed interval carcinomas, it remains challenging to observe parameters that determine this difference between 'true' interval carcinomas and screen-detected lesions.

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Year:  2010        PMID: 20081807     DOI: 10.1038/modpathol.2009.188

Source DB:  PubMed          Journal:  Mod Pathol        ISSN: 0893-3952            Impact factor:   7.842


  3 in total

1.  Copy number imbalances between screen- and symptom-detected breast cancers and impact on disease-free survival.

Authors:  A M Brewster; P Thompson; A A Sahin; K Do; M Edgerton; J L Murray; S Tsavachidis; R Zhou; Y Liu; L Zhang; G Mills; M Bondy
Journal:  Cancer Prev Res (Phila)       Date:  2011-07-27

2.  Differential expression of prognostic biomarkers between interval and screen-detected breast cancers: does age or family history matter?

Authors:  Jan T Lowery; Tim Byers; John Kittelson; John E Hokanson; Judy Mouchawar; John Lewin; Dan Merrick; Lisa Hines; Meenakshi Singh
Journal:  Breast Cancer Res Treat       Date:  2011-03-24       Impact factor: 4.872

3.  Interval cancers after skin cancer screening: incidence, tumour characteristics and risk factors for cutaneous melanoma.

Authors:  J Hübner; A Waldmann; A C Geller; M A Weinstock; N Eisemann; M Noftz; S Bertram; S Nolte; B Volkmer; R Greinert; E Breitbart; A Katalinic
Journal:  Br J Cancer       Date:  2016-11-29       Impact factor: 7.640

  3 in total

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