Volume 38, Issue 6 e15335
ORIGINAL ARTICLE

Banff-based histologic chronicity index is associated with graft failure but has poor interobserver reproducibility

Wei-Chou Lin

Wei-Chou Lin

Department of Pathology, National Taiwan University Hospital, Taipei, Taiwan

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Mei-Chin Wen

Mei-Chin Wen

Department of Pathology, China Medical University Hsinchu Hospital, Hsinchu, Taiwan

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Yong-Chen Hsu

Yong-Chen Hsu

Department of Pathology and Laboratory Medicine, Taichung Veterans General Hospital, Taichung, Taiwan

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Chien-Yi Kuo

Chien-Yi Kuo

Department of Anatomic Pathology, Chang Gung Memorial Hospital Linkou Main Branch, Taoyuan, Taiwan

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Tai-Di Chen

Corresponding Author

Tai-Di Chen

Department of Anatomic Pathology, Chang Gung Memorial Hospital Linkou Main Branch, Taoyuan, Taiwan

School of Medicine, National Tsing Hua University, Hsinchu, Taiwan

Correspondence

Tai-Di Chen, Department of Anatomic Pathology, Chang Gung Memorial Hospital Linkou Main Branch, Taoyuan 333423, Taiwan.

Email: [email protected]

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First published: 28 May 2024

Abstract

Background

Antibody-mediated rejection (AMR) often leads to chronic kidney allograft damage and is a critical cause of allograft failure. The Banff classification, used to diagnose AMR, has become complex and challenging for clinicians. A Banff-based histologic chronicity index (CI) was recently proposed as a simplified prognostic indicator. Its reliability and reproducibility have not been externally validated.

Methods

This study investigated 71 kidney allograft biopsies diagnosed with AMR. Interobserver reproducibility of the recently proposed CI and its components (cg, cv, ct, and ci) were assessed. The association between CI and allograft failure was analyzed, and CI cut-off values were evaluated by Cox proportional hazards regression and Kaplan–Meier estimator with log-rank test.

Results

The study confirmed the association of CI with allograft failure, but also revealed that the assessment of CI varied between pathologists, impacting its reproducibility as a prognostic tool. Only 49 (69.0%) of the biopsies showed complete agreement on the proposed cut-off value of CI < 4 or CI ≥ 4. Furthermore, this cut-off did not reliably stratify allograft failure. Notably, the cg score, which carries significant weight in the CI calculation, had the lowest agreement between observers (kappa = .281).

Conclusions

While a simplified prognostic indicator for AMR is needed, this study highlights the limitations of CI, particularly its poor interobserver reproducibility. Our findings suggest that clinicians should interpret CI cautiously and consider establishing their own cut-off values. This study underscores the need to address interobserver reproducibility before CI can be widely adopted for AMR management.

CONFLICT OF INTEREST STATEMENT

The authors declare no conflicts of interest.

DATA AVAILABILITY STATEMENT

The data underlying this article will be shared upon reasonable request to the corresponding author.

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