Evidence map›Paper›PMID 40450177›Full record

ReviewMolecular diagnosis & therapy2025

Evaluation of Minimal Residual Disease in Patients with Neuroblastoma.

Nobuyuki Yamamoto, Kikyo Ishizawa, Mayuno Umemoto, Akihiro Nishimura, Tomoko Fujikawa, Shotaro Inoue, Naoko Nakatani, Akihiro Tamura, Nanako Nino, Suguru Uemura and 3 more

Abstract readReview
In one paragraph

Review in Molecular diagnosis & therapy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
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

13 authors.

Nobuyuki YamamotoDepartment of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Japan.
Kikyo IshizawaDepartment of Public Health, Kobe University Graduate School of Health Science, 7-10-2 Tomogaoka, Suma-ku, Kobe, 654-0142, Japan.
Mayuno UmemotoDepartment of Public Health, Kobe University Graduate School of Health Science, 7-10-2 Tomogaoka, Suma-ku, Kobe, 654-0142, Japan.
Akihiro NishimuraDepartment of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Japan.
Tomoko FujikawaDepartment of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Japan.
Shotaro InoueDepartment of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Japan.
Naoko NakataniDepartment of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Japan.
Akihiro TamuraDepartment of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Japan.
Nanako NinoDepartment of Hematology and Oncology, Kobe Children Hospital, Kobe, Japan.
Suguru UemuraDepartment of Hematology and Oncology, Kobe Children Hospital, Kobe, Japan.
Daiichiro HasegawaDepartment of Hematology and Oncology, Kobe Children Hospital, Kobe, Japan.
Yoshiyuki KosakaDepartment of Hematology and Oncology, Kobe Children Hospital, Kobe, Japan.
Noriyuki NishimuraDepartment of Public Health, Kobe University Graduate School of Health Science, 7-10-2 Tomogaoka, Suma-ku, Kobe, 654-0142, Japan. nnishi@med.kobe-u.ac.jp.ORCID 0000-0002-9000-4341

Funding

Japan Society for the Promotion of Science 21K07750Japan Society for the Promotion of Science 23K14977
6 · The paper itself

Abstract

Neuroblastoma (NB) is a pediatric extracranial solid tumor that accounts for approximately 15% of all pediatric cancer deaths. More than 50% of patients with newly diagnosed NB are classified into a high-risk group with an approximately 50% long-term survival rate. Although most high-risk patients with NB achieve remission, more than half may have minimal residual disease (MRD) that eventually causes relapse. Looking towards an optimal outcome, the accurate evaluation of MRD in patients with NB (NB-MRD) is essential to monitor the treatment response and disease burden. Over the past decades, the quantification of NB-associated messenger RNA (NB-mRNA) by reverse transcriptase-polymerase chain reaction has become widely used to detect NB-MRD, owing to the lack of recurrent genomic aberrations in NB cells. To achieve a more accurate and sensitive detection, the current NB-MRD assays quantify a set of NB-mRNAs to detect NB cells in bone marrow, peripheral blood, and peripheral blood stem cell samples. Among a growing number of NB-MRD assays, several assays quantitating different but overlapping sets of NB-mRNAs are reported to have a significant prognostic value. However, the clinical significance of NB-MRD remains to be established. In this review, we summarize the recent progress in NB-MRD and evaluate its clinical value.

Indexed as

Neoplasm, ResidualNeuroblastomaBiomarkers, TumorHumansPrognosisRNA, MessengerBiomarkers, TumorRNA, Messenger

Identifiers

PMID40450177
PMCPMC12227348

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Registered trials

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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.