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Development of an AI-Assisted Diagnostic Tool for Mycosis Fungoides and Other Cutaneous Lymphoproliferative Diseases Using Microscopic Image Analysis: A Training and Validation Study

14. juli 2026 opdateret af: Kariman Mostafa Sayed Mansour, Cairo University

Cutaneous lymphoproliferative diseases (CLPDs) are a group of skin disorders that range from benign conditions, such as pseudolymphomas, to malignant forms like cutaneous T-cell and B-cell lymphomas. Mycosis fungoides is the most common malignant type, but diagnosis is often difficult because many benign skin conditions can mimic lymphoma. Current diagnostic methods rely on microscopic examination of biopsies, which can be subjective and vary between pathologists.

This study aims to develop and validate a deep learning model that uses digitized biopsy images and clinical data to distinguish malignant CLPDs from benign ones. By applying artificial intelligence to dermatopathology, the project seeks to improve diagnostic accuracy, reduce variability, and support clinicians in making timely treatment decisions. The novelty of this work lies in applying advanced AI methods to a rare and challenging group of skin diseases, with the potential to enhance patient care in both specialized centers and resource-limited settings.

Studieoversigt

Detaljeret beskrivelse

Cutaneous lymphoproliferative diseases (CLPDs) encompass both benign and malignant disorders, ranging from pseudolymphomas to cutaneous T-cell and B-cell lymphomas. Mycosis fungoides (MF) is the most common malignant subtype, but diagnosis is often challenging because benign inflammatory conditions can closely mimic lymphoma. Histopathological examination remains the gold standard, yet interpretation is subjective and prone to inter-observer variability. This highlights the need for standardized diagnostic tools, including artificial intelligence (AI) solutions.

This study is a retrospective diagnostic accuracy investigation using routinely collected data. Archived hematoxylin and eosin (H&E) stained slides of patients with MF and other CLPDs will be retrieved from the Dermatopathology Unit at Kasr Al-Aini Hospitals, Cairo University. Slides of benign mimickers such as pseudolymphoma and pityriasis lichenoides will also be included. Cases with poor slide quality or insufficient data will be excluded.

Digitized images will be captured using both high-resolution microscope cameras and standardized smartphone devices to evaluate feasibility. Experienced dermatopathologists will annotate regions of interest, and relevant clinical data will be extracted to build a structured database. Deep learning models, particularly convolutional neural networks (CNNs), will be trained and validated on these datasets. Preprocessing techniques such as color normalization, stain separation, and data augmentation will be applied to enhance robustness.

The primary outcomes are diagnostic accuracy, sensitivity, specificity, and predictive values of the AI models in differentiating malignant from benign CLPDs, and in staging MF. Secondary outcomes include comparison with expert dermatopathologists, assessment of smartphone-based imaging, and evaluation across magnification levels. More than 500 slides collected over the past five years will be used, divided into training, validation, and testing sets.

By integrating AI into dermatopathology, this study aims to reduce diagnostic variability, improve accuracy, and explore novel imaging approaches. The work represents one of the first applications of deep learning to CLPDs, with potential to enhance patient care in both specialized centers and resource-limited healthcare settings.

Undersøgelsestype

Observationel

Tilmelding (Anslået)

463

Kontakter og lokationer

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Studiesteder

      • Cairo, Egypten
        • Kasr Al-Aini Hospitals, Cairo University

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

  • Barn
  • Voksen
  • Ældre voksen

Tager imod sunde frivillige

N/A

Prøveudtagningsmetode

Ikke-sandsynlighedsprøve

Studiebefolkning

Archived slides of patients diagnosed with malignant CLPDs (e.g., mycosis fungoides, cutaneous B-cell lymphoma) and benign mimickers (e.g., pseudolymphoma, pityriasis lichenoides chronica, PLEVA) were identified from the pathology database of Kasr Al-Aini Hospitals, Cairo University.

Cases were selected based on WHO-EORTC diagnostic criteria and availability of adequate quality H&E slides plus relevant clinical data.

Beskrivelse

Inclusion Criteria:

  • Archived slides of patients with a confirmed histopathological diagnosis of malignant CLPDs (e.g., mycosis fungoides at all stages, cutaneous B-cell lymphoma, primary cutaneous anaplastic large cell lymphoma, lymphomatoid papulosis), based on WHO-EORTC criteria.
  • Archived slides of patients with benign CLPDs that mimic MF clinically and histologically (e.g., pseudolymphoma, pityriasis lichenoides chronica, pityriasis lichenoides et varioliformis acuta [PLEVA]).
  • Availability of adequate quality hematoxylin and eosin (H&E) stained slides.
  • Availability of relevant clinical data (age, sex, disease duration, distribution of lesions, drug history).

Exclusion Criteria:

  • Slides with significant artifacts (folding, tearing, poor staining) that prevent adequate image analysis.
  • Cases with insufficient clinical or pathological data for definitive diagnosis.
  • Cases with secondary cutaneous CLPDs

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

Kohorter og interventioner

Gruppe / kohorte
Intervention / Behandling
MF
Patients diagnosed histopathologically as mycosis fungoides

Development and validation of a deep learning model using digitized hematoxylin and eosin (H&E) stained slides and clinical data to differentiate malignant CLPDs from benign mimickers.

Comparator: Standard histopathological diagnosis by experienced dermatopathologists.

PLC/PLEVA
Patients diagnosed histopathologically as PLC or PLEVA

Development and validation of a deep learning model using digitized hematoxylin and eosin (H&E) stained slides and clinical data to differentiate malignant CLPDs from benign mimickers.

Comparator: Standard histopathological diagnosis by experienced dermatopathologists.

TCD
Patients diagnosed histopathologically as T cell dyscrasia

Development and validation of a deep learning model using digitized hematoxylin and eosin (H&E) stained slides and clinical data to differentiate malignant CLPDs from benign mimickers.

Comparator: Standard histopathological diagnosis by experienced dermatopathologists.

BCL
Patients diagnosed histopathologically as B cell lymphoma

Development and validation of a deep learning model using digitized hematoxylin and eosin (H&E) stained slides and clinical data to differentiate malignant CLPDs from benign mimickers.

Comparator: Standard histopathological diagnosis by experienced dermatopathologists.

Pseudolymphoma
Patients diagnosed histopathologically as pseudo lymphoma

Development and validation of a deep learning model using digitized hematoxylin and eosin (H&E) stained slides and clinical data to differentiate malignant CLPDs from benign mimickers.

Comparator: Standard histopathological diagnosis by experienced dermatopathologists.

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Diagnostic accuracy of AI model
Tidsramme: Baseline (In retrospective diagnostic studies, the moment the AI evaluates the historical slide is considered the patients's baseline).
Accuracy, sensitivity, specificity, and positive predictive value of the trained AI models in differentiating benign CLPDs from malignant types.
Baseline (In retrospective diagnostic studies, the moment the AI evaluates the historical slide is considered the patients's baseline).

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Comparison with dermatopathologists
Tidsramme: Baseline (In retrospective diagnostic studies, the moment the AI evaluates the historical slide is considered the patients's baseline).
Compare AI model diagnostic accuracy with that of experienced dermatopathologists
Baseline (In retrospective diagnostic studies, the moment the AI evaluates the historical slide is considered the patients's baseline).
Smartphone imaging feasibility
Tidsramme: Baseline (In retrospective diagnostic studies, the moment the AI evaluates the historical slide is considered the patients's baseline).
Assess feasibility and diagnostic accuracy of AI models using smartphone-captured histopathology images.
Baseline (In retrospective diagnostic studies, the moment the AI evaluates the historical slide is considered the patients's baseline).

Samarbejdspartnere og efterforskere

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Publikationer og nyttige links

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Generelle publikationer

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Faktiske)

1. januar 2026

Primær færdiggørelse (Anslået)

30. november 2026

Studieafslutning (Anslået)

30. december 2026

Datoer for studieregistrering

Først indsendt

30. juni 2026

Først indsendt, der opfyldte QC-kriterier

14. juli 2026

Først opslået (Faktiske)

15. juli 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

15. juli 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

14. juli 2026

Sidst verificeret

1. januar 2026

Mere information

Begreber relateret til denne undersøgelse

Andre undersøgelses-id-numre

  • MD-152-2025

Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter

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Kliniske forsøg med AI-assisted histopathology image analysis

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