Evidence map›Paper›PMID 42094139›Full record

ArticlemedRxiv : the preprint server for health sciences2026

Feasibility of Non-Sedated Multispectral Neuroimaging in Newly Diagnosed Children with Leukemia.

Mary-Kaylin Tran, Lauren Appell, Simon Chung, Madison Sanders, Amy Jones, Mandy Fenwick, Elizabeth Oest, Xiawei Ou, Jason Farrar, Andrew W Brown and 2 more

Abstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Mary-Kaylin TranArkansas Children's Research Institute, Little Rock, Arkansas, USA.
Lauren AppellArkansas Children's Research Institute, Little Rock, Arkansas, USA.ORCID 0000-0001-5147-8328
Simon ChungArkansas Children's Research Institute, Little Rock, Arkansas, USA.ORCID 0000-0003-2349-3779
Madison SandersArkansas Children's Research Institute, Little Rock, Arkansas, USA.
Amy JonesArkansas Children's Research Institute, Little Rock, Arkansas, USA.
Mandy FenwickArkansas Children's Research Institute, Little Rock, Arkansas, USA.
Elizabeth OestArkansas Children's Research Institute, Little Rock, Arkansas, USA.
Xiawei OuArkansas Children's Research Institute, Little Rock, Arkansas, USA.ORCID 0000-0001-9815-0127
Jason FarrarArkansas Children's Research Institute, Little Rock, Arkansas, USA.ORCID 0000-0003-2148-5839
Andrew W BrownArkansas Children's Research Institute, Little Rock, Arkansas, USA.ORCID 0000-0002-1758-8205
Timothy R KoscikArkansas Children's Research Institute, Little Rock, Arkansas, USA.ORCID 0000-0002-2551-8127
Ellen van der PlasArkansas Children's Research Institute, Little Rock, Arkansas, USA.ORCID 0000-0002-7490-6636

Funding

Identifying markers of abnormal neurocognitive trajectories during chemotherapy treatment of childhood acute lymphoblastic leukemiaR37CA266135 · NCI · ARKANSAS CHILDREN'S HOSPITAL RES INST · PI Ellen van der Plas · 2022 to 2026
$2.5M
NCI NIH HHS R37 CA266135
6 · The paper itself

Abstract

Introduction: Children with acute lymphoblastic leukemia (ALL) require neurotoxic treatment during critical periods of brain development. Multispectral magnetic resonance imaging (MRI) offers opportunities to characterize the impact of chemotherapy on the developing brain, but this has been constrained by concerns regarding feasibility of obtaining quality MRIs from these critically ill children at a young age. Our goal is to demonstrate a framework for improving the feasibility of non-sedated, multispectral MRI in newly diagnosed ALL patients. Methods: Participants were enrolled from August 2023 through February 2026, and included newly diagnosed ALL patients and controls recruited from the community ages 3-10 years old. Participants completed a series of three non-sedated MRI without contrast on a 3T scanner over 12 months. Sequences included anatomical T1-weighted and QALAS sequences for quantitative mapping, diffusion weighted MRI (DWI), MR Spectroscopy (MRS), and resting-state functional MRI (rs-fMRI). A sequence was considered complete if data quality was sufficient for successful image processing. Mixed-effects logistic regression models were used determine if group and study visit were associated with MRI success rates across sequences. Results: The sample included 17 ALL patients and 30 controls, who contributed to 38 and 75 observations, respectively. Of 113 attempted scans, 105 had ≥1 sequence completed (93%). Across assessments, ALL patients were less likely to complete a scan (31 of 38 attempts; raw rate: 82%) relative to controls (73 of 75; raw rate: 96%; model-estimated difference=-14.1%, 95%CI=-27.1%; -1.1%, p=0.033). Baseline success rate was 65% (11 of 17) for ALL patients and 93% (28 of 30) for controls (model-estimated difference=-26.8%, 95%CI=-52.7%; -0.9%, p=0.42); however, nearly all T1w scans in ALL patients were successful at follow-up visits (20 of 21; 95%), with no significant differences between groups (model-estimated difference at followup 1=-2.1%, 95%CI=-11.7%; 7.6%; model-estimated difference at follow-up 2=-8.3%, 95%CI=-26.3%; 9.6%). A similar pattern was observed for DWI, MRS and rs-fMRI sequences with relatively high completion rates at follow-up assessments. Discussion: Non-sedated multispectral MRI is feasible in young children with newly diagnosed ALL, particularly with repeated visits and structured behavioral preparation. These results highlight opportunities to capture the scope and depth of neurodevelopmental changes concurrent with ALL treatment.

Indexed as

acute lymphoblastic leukemiabrainmagnetic resonance imagingNeuroimagingnon-sedated

Identifiers

PMID42094139
PMCPMC13142564

What OpenQuestion holds

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LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.