Evidence map›Paper›PMID 41229491›Full record

ArticleFrontiers in oncology2025

The prognostic significance of incomplete hematological recovery in pediatric patients with low/intermediate risk AML and negative MRD after induction 1.

Nessma M Shahin, Mahmoud Hammad, Hanafy Hafez, Sherine Salem, Nahla El-Sharkawy, Amr Elnashar, Leslie Lehmann, Alaa El-Haddad

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Article in Frontiers in oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Nessma M ShahinDepartment of Pediatric Oncology, Children Cancer Hospital (57357), Cairo, Egypt.
Mahmoud HammadDepartment of Pediatric Oncology, National Cancer Institute, Cairo University, Cairo, Egypt.
Hanafy HafezDepartment of Pediatric Oncology, National Cancer Institute, Cairo University, Cairo, Egypt.
Sherine SalemDepartment of Clinical Pathology, Children Cancer Hospital (57357), Cairo, Egypt.
Nahla El-SharkawyDepartment of Clinical Pathology, Children Cancer Hospital (57357), Cairo, Egypt.
Amr ElnasharDepartment of Clinical Research, Children Cancer Hospital (57357), Cairo, Egypt.
Leslie LehmannPediatric Oncology, Harvard Medical School, Boston Children's Hospital, Dana-Farber Cancer Institute, Boston, MA, United States.
Alaa El-HaddadDepartment of Pediatric Oncology, Children Cancer Hospital (57357), Cairo, Egypt.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Pediatric acute myeloid leukemia (AML) accounts for approximately 25% of childhood hematologic malignancies. Outcomes have markedly improved, especially in low-risk and intermediate-risk patients, with overall survival (OS) rates approaching 80-85%. Prognosis is primarily determined by cytogenetic/molecular risk and minimal residual disease (MRD) status following induction therapy. While complete remission (CR) traditionally requires morphologic clearance of leukemia with full hematologic recovery, some patients achieve morphologic remission with incomplete recovery (CRi). Although adult studies associate CRi with poor prognosis, its relevance in MRD-negative pediatric AML remains unclear. This study evaluates the prognostic significance of hematologic recovery in MRD-negative, low/intermediate-risk pediatric AML. Methods: We conducted a retrospective analysis of 120 pediatric AML patients treated at CCHE-57357 between 2012 and 2020 who achieved MRD negativity (<0.1% by 8-10 color flow cytometry) after Induction I. Risk stratification followed WHO/ELN guidelines. For exploratory purposes, intermediate-risk patients with MRD <0.1% were reclassified as "MRD-defined low risk." Patients were categorized by hematologic recovery: CR (ANC ≥1000/µL, platelets ≥100,000/µL), partial hematological recovery (CRh) (ANC ≥500/µL and/or platelets ≥50,000/µL), and CRi (ANC 500/µL and/or platelets <50,000/µL). Outcomes included OS, relapse-free survival (RFS), and event-free survival (EFS). Results: Among 120 patients (median age 8.5 years), 25 (21%) achieved CR, 17 (14.3%) CRh, and 78 (64.7%) CRi. CRi patients had numerically lower 5-year OS (63.3%) compared to CRh (76%) and CR (71.8%), though differences were not statistically significant. Platelet recovery alone (complete Platelet recovery (CRp) vs incomplete platelet recovery (CRip) showed a trend toward prognostic relevance (5-year OS: 73.3% vs 57.1%), also non-significant. Infectious complications were common: six sepsis-related deaths occurred in the low-risk group and four in the standard-risk group, with ICU admissions disproportionately higher in standard-risk patients (12 vs 1). CRi patients experienced longer hospital stays and required more transfusion support. Conclusion: In MRD-negative pediatric AML, incomplete hematologic recovery did not significantly predict inferior survival, though trends suggest potential prognostic value-particularly in low-risk patients. CRi may reflect treatment-related toxicity or infectious complications rather than residual disease. These findings support a more nuanced interpretation of remission depth and highlight the need for larger, multi-institutional studies incorporating molecular risk refinement and clinical context.

Indexed as

complete remission (CR)incomplete remission (CRi)minimal residual disease (MRD)morphological remissionpediatric acute myeloid leukemia (AML)

Identifiers

PMID41229491
PMCPMC12602198

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