Development of an Artificial-Intelligence-Based Tool for Automated Assessment of Cellularity in Bone Marrow Biopsies in Ph-Negative Myeloproliferative Neoplasms

Author:

D’Abbronzo Giuseppe1,D’Antonio Antonio2,De Chiara Annarosaria3,Panico Luigi4,Sparano Lucianna5,Diluvio Anna1,Sica Antonello6ORCID,Svanera Gino7,Franco Renato18ORCID,Ronchi Andrea18

Affiliation:

1. Department of Mental and Physical Health and Preventive Medicine, Università degli Studi della Campania “Luigi Vanvitelli”, 80138 Naples, Italy

2. Pathology Unit, Hospital “Ospedale del Mare”, 80147 Naples, Italy

3. Histopathology of lymphomas and Sarcoma SSD, Istituto Nazionale dei Tumori I.R.C.C.S. Fondazione “Pascale”, 80131 Naples, Italy

4. Pathology Unit, Hospital “Monaldi”, 80131 Naples, Italy

5. Pathology Unit, Hospital “Andrea Tortora”, 82100 Pagani, Italy

6. Haematology and Oncology Unit, Vanvitelli Hospital, 80131 Naples, Italy

7. Haematology Unit, ASL Na2 North, 80014 Giugliano, Italy

8. Pathology Unit, Vanvitelli Hospital, 80138 Naples, Italy

Abstract

The cellularity assessment in bone marrow biopsies (BMBs) for the diagnosis of Philadelphia chromosome (Ph)-negative myeloproliferative neoplasms (MPNs) is a key diagnostic feature and is usually performed by the human eyes through an optical microscope with consequent inter-observer and intra-observer variability. Thus, the use of an automated tool may reduce variability, improving the uniformity of the evaluation. The aim of this work is to develop an accurate AI-based tool for the automated quantification of cellularity in BMB histology. A total of 55 BMB histological slides, diagnosed as Ph- MPN between January 2018 and June 2023 from the archives of the Pathology Unit of University “Luigi Vanvitelli” in Naples (Italy), were scanned on Ventana DP200 or Epredia P1000 and exported as whole-slide images (WSIs). Fifteen BMBs were randomly selected to obtain a training set of AI-based tools. An expert pathologist and a trained resident performed annotations of hematopoietic tissue and adipose tissue, and annotations were exported as .tiff images and .png labels with two colors (black for hematopoietic tissue and yellow for adipose tissue). Subsequently, we developed a semantic segmentation model for hematopoietic tissue and adipose tissue. The remaining 40 BMBs were used for model verification. The performance of our model was compared with an evaluation of the cellularity of five expert hematopathologists and three trainees; we obtained an optimal concordance between our model and the expert pathologists’ evaluation, with poorer concordance for trainees. There were no significant differences in cellularity assessments between two different scanners.

Publisher

MDPI AG

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