# Developing organ dysfunction diagnostic criteria for children with cancer and post-hematopoietic cell transplantation: protocol of systematic review

**Authors:** Michael Bashir, Sayeda Islam, Jordan Wrigley, Anita Arias, Roelie M. Wösten-van Asperen, Kimberly K. Kertis, Melissa M. Hudson, Courtney M. Rowan, Aimee C. Talleur, Joshua Wolf, Benjamin Oelkers, Melissa R. Hines, Asya Agulnik

PMC · DOI: 10.3389/fonc.2025.1591263 · Frontiers in Oncology · 2025-10-15

## TL;DR

This study aims to improve organ dysfunction criteria for children with cancer and those who had hematopoietic cell transplants, as existing criteria may not be accurate for these patients.

## Contribution

The study introduces a protocol to adapt the PODIUM criteria for pediatric oncology and post-HCT patients using a systematic review and Delphi process.

## Key findings

- Current PODIUM criteria may misclassify organ dysfunction in pediatric oncology and post-HCT patients.
- A systematic review will identify evidence-based criteria for organ dysfunction in these patients.
- A modified Delphi process will be used to develop tailored criteria (PODIUM-Onc).

## Abstract

The Pediatric Organ Dysfunction Information Update Mandate (PODIUM) proposed consensus criteria to define organ dysfunction in critically ill children. However, utilization of the PODIUM criteria in pediatric oncology patients and those who have received hematopoietic cell transplantation or cellular therapy (post-HCT/CAR) may inaccurately classify organ dysfunction in these patients due to differences in organ dysfunction etiology, pathophysiology, and risk factors for adverse outcomes. To address this gap, we report a study protocol to systematically review the performance of the PODIUM criteria for pediatric cancer and/or those treated with HCT and determine if adjustments are needed.

The objectives of this study will be to [1] identify evidence-based criteria for organ dysfunction predicting adverse outcomes among pediatric oncology and post-HCT patients, [2] use these findings to inform adapted consensus criteria (PODIUM-Onc) for organ dysfunction tailored to this high-risk population through a multidisciplinary modified Delphi process, and [3] describe knowledge gaps to guide future research.

We will perform a systematic literature review of studies published since January 1, 2004, using the following databases: MEDLINE (via PubMed), CINAHL (via EBSCO), EMBASE (via Elsevier), and Web of Science (via Clarivate). Search results will be filtered using a pediatric search hedge and further refined to children (0 to 21 years old) during or up to 1 year after treatment for cancer or HCT/CAR for malignancy. Publications without original data (e.g., comments, editorials, letters, notes, conference materials), studies with ≤ 10 patients, and those preceding January 1, 2004, will be excluded.

We will include original studies in any language published since January 1, 2004, that meet all eligibility criteria and for which a full text is available.

Data extraction will include information related to study characteristics, hospital characteristics, underlying population characteristics, patient population characteristics, and outcomes.

We will extract and report data on the study, hospital, and patient characteristics, outcomes, and risk of bias.

By systematically reviewing and analyzing organ-specific factors associated with patient outcomes and synthesizing these findings through a modified Delphi consensus process, we aim to create consensus criteria that will be clinically relevant for pediatric oncology patients and HCT patients. These criteria will provide a foundation to guide clinical care and to support future research in this vulnerable patient population.

## Linked entities

- **Diseases:** cancer (MONDO:0004992)

## Full-text entities

- **Diseases:** cancer (MESH:D009369), Organ Dysfunction (MESH:D009102), critically ill (MESH:D016638)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

30 references — full list in the complete paper: https://tomesphere.com/paper/PMC12568018/full.md

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Source: https://tomesphere.com/paper/PMC12568018