Evidence map›Paper›PMID 36135021›Full record

ArticleBioengineering (Basel, Switzerland)2022

NDG-CAM: Nuclei Detection in Histopathology Images with Semantic Segmentation Networks and Grad-CAM.

Nicola Altini, Antonio Brunetti, Emilia Puro, Maria Giovanna Taccogna, Concetta Saponaro, Francesco Alfredo Zito, Simona De Summa, Vitoantonio Bevilacqua

Abstract read
In one paragraph

Article in Bioengineering (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–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.

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

11 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
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

8 authors.

Nicola AltiniDepartment of Electrical and Information Engineering (DEI), Polytechnic University of Bari, Via Edoardo Orabona n.4, 70126 Bari, BA, Italy.ORCID 0000-0001-7353-4968
Antonio BrunettiDepartment of Electrical and Information Engineering (DEI), Polytechnic University of Bari, Via Edoardo Orabona n.4, 70126 Bari, BA, Italy.ORCID 0000-0002-1934-0983
Emilia PuroDepartment of Electrical and Information Engineering (DEI), Polytechnic University of Bari, Via Edoardo Orabona n.4, 70126 Bari, BA, Italy.
Maria Giovanna TaccognaDepartment of Electrical and Information Engineering (DEI), Polytechnic University of Bari, Via Edoardo Orabona n.4, 70126 Bari, BA, Italy.
Concetta SaponaroLaboratory of Preclinical and Translational Research, Centro di Riferimento Oncologico della Basilicata (IRCCS-CROB), Via Padre Pio n.1, 85028 Rionero in Vulture, PZ, Italy.ORCID 0000-0002-8196-3583
Francesco Alfredo ZitoPathology Department, IRCCS Istituto Tumori "Giovanni Paolo II", Via O. Flacco n.65, 70124 Bari, BA, Italy.ORCID 0000-0003-4140-4020
Simona De SummaMolecular Diagnostics and Pharmacogenetics Unit, IRCCS Istituto Tumori "Giovanni Paolo II", Via O. Flacco n.65, 70124 Bari, BA, Italy.ORCID 0000-0001-9607-3754
Vitoantonio BevilacquaDepartment of Electrical and Information Engineering (DEI), Polytechnic University of Bari, Via Edoardo Orabona n.4, 70126 Bari, BA, Italy.ORCID 0000-0002-3088-0788

Funding

Regione Puglia CUP B84I18000540002
6 · The paper itself

Abstract

Nuclei identification is a fundamental task in many areas of biomedical image analysis related to computational pathology applications. Nowadays, deep learning is the primary approach by which to segment the nuclei, but accuracy is closely linked to the amount of histological ground truth data for training. In addition, it is known that most of the hematoxylin and eosin (H&E)-stained microscopy nuclei images contain complex and irregular visual characteristics. Moreover, conventional semantic segmentation architectures grounded on convolutional neural networks (CNNs) are unable to recognize distinct overlapping and clustered nuclei. To overcome these problems, we present an innovative method based on gradient-weighted class activation mapping (Grad-CAM) saliency maps for image segmentation. The proposed solution is comprised of two steps. The first is the semantic segmentation obtained by the use of a CNN; then, the detection step is based on the calculation of local maxima of the Grad-CAM analysis evaluated on the nucleus class, allowing us to determine the positions of the nuclei centroids. This approach, which we denote as NDG-CAM, has performance in line with state-of-the-art methods, especially in isolating the different nuclei instances, and can be generalized for different organs and tissues. Experimental results demonstrated a precision of 0.833, recall of 0.815 and a Dice coefficient of 0.824 on the publicly available validation set. When used in combined mode with instance segmentation architectures such as Mask R-CNN, the method manages to surpass state-of-the-art approaches, with precision of 0.838, recall of 0.934 and a Dice coefficient of 0.884. Furthermore, performance on the external, locally collected validation set, with a Dice coefficient of 0.914 for the combined model, shows the generalization capability of the implemented pipeline, which has the ability to detect nuclei not only related to tumor or normal epithelium but also to other cytotypes.

Indexed as

deep learningGrad-CAMhistopathologyinstance segmentationnuclei detectionnuclei segmentationsemantic segmentation

Identifiers

PMID36135021
PMCPMC9495364

What OpenQuestion holds

Textmetadata
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.