Literature DB >> 24704158

Automated quantification of MART1-verified Ki-67 indices: useful diagnostic aid in melanocytic lesions.

Patricia Switten Nielsen1, Eva Spaun2, Rikke Riber-Hansen2, Torben Steiniche2.   

Abstract

The MART1-verified Ki-67 proliferation index is a valuable aid to distinguish melanomas from nevi. Because such indices are quantifiable by image analysis, they may provide a novel automated diagnostic aid. This study aimed to validate the diagnostic performance of automated dermal Ki-67 indices and to explore the diagnostic capability of epidermal Ki-67 in lesions both with and without a dermal component. In addition, we investigated the automated indices' ability to predict sentinel lymph node (SLN) status. Paraffin-embedded tissues from 84 primary cutaneous melanomas (35 with SLN biopsy), 22 melanoma in situ, and 270 nevi were included consecutively. Whole slide images were captured from Ki-67/MART1 double stains, and image analysis computed Ki-67 indices for epidermis and dermis. In lesions with a dermal component, the area under the receiver operating characteristic (ROC) curve was 0.79 (95% confidence interval [CI], 0.72-0.86) for dermal indices. By excluding lesions with few melanocytic cells, this area increased to 0.93 (95% CI, 0.88-0.98). A simultaneous analysis of epidermis and dermis yielded an ROC area of 0.94 (95% CI, 0.91-0.96) for lesions with a dermal component and 0.98 (95% CI, 0.97-1.0) for lesions with a considerable dermal component. For all lesions, the ROC area of the simultaneous analysis was 0.89 (95% CI, 0.85-0.92). SLN-positive patients generally had a higher index than SLN-negative patients (P ≤ .003). Conclusively, an automated diagnostic aid seems feasible in melanocytic pathology. The dermal Ki-67 index was inferior to a combined epidermal and dermal index in diagnosis but valuable for predicting the SLN status of our melanoma patients.
Copyright © 2014 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Computer-assisted image analysis; Diagnosis; Immunohistochemical double staining; Ki-67; Melanocytic lesions; Melanoma; Proliferation index

Mesh:

Substances:

Year:  2014        PMID: 24704158     DOI: 10.1016/j.humpath.2014.01.009

Source DB:  PubMed          Journal:  Hum Pathol        ISSN: 0046-8177            Impact factor:   3.466


  4 in total

1.  Tumor Cell Adhesion As a Risk Factor for Sentinel Lymph Node Metastasis in Primary Cutaneous Melanoma.

Authors:  Alexander Meves; Ekaterina Nikolova; Joel B Heim; Edwin J Squirewell; Mark A Cappel; Mark R Pittelkow; Clark C Otley; Nille Behrendt; Ditte M Saunte; Jorgen Lock-Andersen; Louis A Schenck; Amy L Weaver; Vera J Suman
Journal:  J Clin Oncol       Date:  2015-07-06       Impact factor: 44.544

2.  Automated quantification of proliferation with automated hot-spot selection in phosphohistone H3/MART1 dual-stained stage I/II melanoma.

Authors:  Patricia Switten Nielsen; Rikke Riber-Hansen; Henrik Schmidt; Torben Steiniche
Journal:  Diagn Pathol       Date:  2016-04-09       Impact factor: 2.644

3.  Multi-Pass Adaptive Voting for Nuclei Detection in Histopathological Images.

Authors:  Cheng Lu; Hongming Xu; Jun Xu; Hannah Gilmore; Mrinal Mandal; Anant Madabhushi
Journal:  Sci Rep       Date:  2016-10-03       Impact factor: 4.379

4.  Attitudes Toward Artificial Intelligence Within Dermatopathology: An International Online Survey.

Authors:  Sam Polesie; Phillip H McKee; Jerad M Gardner; Martin Gillstedt; Jan Siarov; Noora Neittaanmäki; John Paoli
Journal:  Front Med (Lausanne)       Date:  2020-10-20
  4 in total

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