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A quantitative method for assessing treatment-related changes within the airway mucosa in patients with chronic bronchitis - 02/01/25

Doi : 10.1016/j.rmed.2024.107889 
William S. Krimsky a, , 1 , Paul A. VanderLaan b, 1 , Jeffrey S. Iding c , David W. Hunter a , Beryl A. Hatton a , Brett Bannan a , Victor Kim d
a Galvanize Therapeutics, Inc., 3200 Bridge Parkway, Redwood City, CA, 94065, USA 
b Department of Pathology, Beth Israel Deaconess Medical Center, Harvard Medical School, 330 Brookline Avenue, Boston, MA, 02215, USA 
c Department of Pathology, MedStar Health, 10980 Grantchester Way, Columbia, MD, 21044, USA 
d Department of Thoracic Medicine and Surgery, Lewis Katz School of Medicine at Temple University, 3500 North Broad Street, Philadelphia, PA, 19140, USA 

Corresponding author. Galvanize Therapeutics, Inc, 3200 Bridge Parkway, Redwood City, CA, 94065, USA.Galvanize Therapeutics, Inc3200 Bridge ParkwayRedwood CityCA94065USA

Abstract

Background

No standardized method has yet been established for evaluating airway mucosal aberrancies associated with chronic obstructive pulmonary disease (COPD) or chronic bronchitis (CB). While goblet cell hyperplasia (GCH) is an established pathognomonic hallmark of the CB disease process, no standardized method exists for acquiring mucosal biopsies and assessing morphologic airway mucosa alterations. Additionally, the impacts from interventions targeting the airway mucosa are not well defined. In this context, a reliable and robust measure for assessing airway mucosa at baseline and subsequent to an intervention is critical for characterizing treatment-related changes.

Research question

Can standardizing airway biopsy tissue collection and histopathological assessment methods generate a robust and repeatable measure to assess airway mucosa tissue characteristics in the setting of COPD/CB?

Study design & methods

Initial tissue collection and histological assessment methods were designed by integrating various aspects from previously published evaluations, applied to an initial tissue sample cohort, and then iteratively refined by independent pathologists.

Results

A standardized metric for histologic airway mucosa assessments was developed that specified tissue collection methods, including re-sampling airways at multiple time points to enable evaluation of treatment-related effects by incorporating scores for GCH, eosinophilia, and chronic inflammation, and the degree of GCH heterogeneity present within each sample.

Conclusion

This multi-center study generated a robust, reproducible approach for assessing airway mucosa aberrancies in the setting of COPD/CB. The iterative approach established consistent tissue specimen recovery and a granular scoring matrix that enabled quantitative scoring of the various tissue findings with substantial histopathologic interrater reliability.

Clinical trial registration number

ClinicalTrials.gov; NCT03107494, NCT04677465; URL: www.clinicaltrials.gov.

Australian New Zealand Clinical Trials Registry (ANZCTR); ACTRN12617000330347; URL: anzctr.org.au.

El texto completo de este artículo está disponible en PDF.

Highlights

No standardized method for assessing airway mucosa in COPD/CB has been developed.
This study established a robust metric for assessing airway aberrancies in COPD/CB.
This method can be used for baseline and repeat assessment of the airway mucosa.
The high interrater reliability enables use in large, multi-center clinical studies.
This approach may be applicable in the assessment of other airway disorders.

El texto completo de este artículo está disponible en PDF.

Keywords : Airway mucosa, Bronchial rheoplasty, Chronic bronchitis, Cryoprobe, Flexible bronchoscope, Goblet cell hyperplasia

Abbreviations : BALT, BR, CB, COPD, FIH, GCH, H&E, PAS, RCT


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© 2024  The Authors. Publicado por Elsevier Masson SAS. Todos los derechos reservados.
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Vol 236

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