# Flow Cytometry-Based Detection of Minimal/Measurable Residual Disease Predicts Survival Outcomes in Pediatrics, Adolescents, and Young Adults With T-acute Lymphoblastic Leukemia

**Authors:** Priyavadhana Balasubramanian, Jay Singh, Amar Ranjan, Pranay Tanwar, Sameer Bakhshi, Anita Chopra

PMC · DOI: 10.7759/cureus.61705 · Cureus · 2024-06-05

## TL;DR

This study shows that detecting minimal residual disease using flow cytometry in T-ALL patients predicts worse survival outcomes in children and young adults.

## Contribution

The study demonstrates the clinical utility of flow cytometry-based MRD detection in T-ALL patients in resource-limited settings.

## Key findings

- PI-MRD positivity was strongly associated with inferior event-free survival (HR = 8.03).
- PI-MRD detection using flow cytometry is a reliable predictor in T-ALL patients.
- Early T-cell precursor ALL was also linked to worse survival outcomes (HR = 2.63).

## Abstract

Background: Measurable/minimal residual disease (MRD) is considered the single most powerful high-risk factor in acute leukemia, including T-cell acute lymphoblastic leukemia (T-ALL). In this study, we evaluated the impact of flow cytometry (FC)-based detection of MRD on survival outcomes in pediatrics, adolescents, and young adults (AYA) with T-ALL.

Methods: We included 139 patients, 88 pediatric patients between the ages of one and 14 years, and 51 AYA patients between 15 and 39 years of age, over a period of three years and were treated with the Indian Collaborative Childhood Leukemia Group (ICiCLe) protocol. MRD assessment was performed on post-induction (PI) bone marrow aspirate samples using a 10-color 11-antibody MRD panel on a Gallios instrument (Beckman Coulter, Miami, FL, USA). MRD value > 0.01% was considered positive. PI-MRD status was available in 131 patients.

Results: The five-year event-free survival (5-year EFS) in PI-MRD positive patients was inferior to those of negative patients (13.56% vs 79.06%), which was statistically significant (P < 0.001). However, the five-year overall survival (5-year OS) did not show any statistically significant difference between PI-MRD positive and negative T-ALL patients (92.93% vs 94.28%). The hazard ratio (HR) for 5-year EFS and MRD positivity was 8.03 (p-value < 0.0001). HR for 5-year EFS and early T-cell precursor ALL (ETP-ALL) was 2.63 (p = -0.02).

Conclusions: PI-MRD detected using FC is a strong predictive factor of inferior survival outcomes in pediatrics, AYA patients with T-ALL. PI-MRD positivity can be used to modify the treatment of T-ALL patients, especially in resource-constrained developing countries where molecular tests are not widely available.

## Linked entities

- **Diseases:** T-cell acute lymphoblastic leukemia (MONDO:0004963), T-acute lymphoblastic leukemia (MONDO:0000871)

## Full-text entities

- **Diseases:** Leukemia (MESH:D007938), ETP-ALL (MESH:D054218), acute leukemia (MESH:D015470), T-acute Lymphoblastic Leukemia (MESH:D054198)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

23 references — full list in the complete paper: https://tomesphere.com/paper/PMC11224933/full.md

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Source: https://tomesphere.com/paper/PMC11224933