# Predicted indirectly recognizable HLA epitopes scores and clinical outcomes after haploidentical stem cell transplantation in pediatric patients with relapsed neuroblastoma

**Authors:** Eun Seop Seo, In Hwa Jeong, Hee Young Ju, Ju Kyung Hyun, Ji Won Lee, Keon Hee Yoo, Won Young Heo, Ki Woong Sung, Hee Won Cho, Eun-Suk Kang

PMC · DOI: 10.3389/fimmu.2025.1517387 · 2025-01-22

## TL;DR

This study shows that higher PIRCHE scores in donor-recipient pairs are linked to better outcomes in pediatric neuroblastoma patients after stem cell transplants.

## Contribution

The study demonstrates the clinical utility of PIRCHE scores in predicting outcomes for pediatric neuroblastoma patients undergoing haplo-SCT.

## Key findings

- Higher PIRCHE-I scores correlate with faster platelet recovery and fewer infections and complications.
- Combined PIRCHE-I and PIRCHE-II scores are strongly associated with improved overall survival.
- PIRCHE-II scores are independently linked to reduced disease progression in multivariable analysis.

## Abstract

The Predicted Indirectly ReCognizable HLA Epitopes (PIRCHE) model is a recently developed algorithm that predicts indirect T-cell recognition by calculating the number of such epitopes in donor-recipient pairs.

In this study, the clinical significance of PIRCHE was evaluated in pediatric patients with relapsed/progressed neuroblastoma undergoing haploidentical stem cell transplantation (haplo-SCT).

A higher PIRCHE-I score was associated with faster platelet recovery (P = 0.007) and lower incidence of hemorrhagic cystitis (13% vs. 41%, P = 0.028) and invasive fungal infections (0% vs. 18%, P = 0.045). Additionally, a higher PIRCHE-I score was significantly associated with better overall survival (OS) (HR 0.57, 95% CI 0.34-0.97, P = 0.038). A higher PIRCHE-II score was associated with better OS (HR 0.57, 95% CI 0.34-0.94, P = 0.028) and reduced progression (HR 0.48, 95% CI 0.30-0.77, P = 0.002). When combined, the PIRCHE-I and PIRCHE-II scores demonstrated an even stronger association with improved OS (HR 0.35, 95% CI 0.15-0.82, P = 0.016). Multivariable analysis confirmed that a higher combined PIRCHE-I and PIRCHE-II score was independently associated with improved OS (combined PIRCHE score HR 0.22, 95% CI 0.06-0.79, P = 0.021), and a higher PIRCHE-II score was significantly associated with reduced progression (HR 0.42, 95% CI 0.25-0.70, P < 0.001).

In conclusion, higher PIRCHE-I and PIRCHE-II scores are linked to better survival outcomes and reduced complications in pediatric haplo-SCT neuroblastoma patients. Incorporating PIRCHE scores into donor selection is expected to optimize transplant outcomes.

## Linked entities

- **Diseases:** neuroblastoma (MONDO:0005072), hemorrhagic cystitis (MONDO:0000496)

## Full-text entities

- **Genes:** HLA-A (major histocompatibility complex, class I, A) [NCBI Gene 3105] {aka HLAA}
- **Diseases:** neuroblastoma (MESH:D009447), hemorrhagic cystitis (MESH:D006470), fungal infections (MESH:D009181)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11833256/full.md

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Source: https://tomesphere.com/paper/PMC11833256