Evidence map›Paper›PMID 37887060›Full record

ArticleBiology2023

Minimal Residual Disease Detected by the 7NB-mRNAs ddPCR Assay Is Associated with Disease Progression in High-Risk Neuroblastoma Patients: A Prospective Multicenter Observational Study in Japan.

Noriyuki Nishimura, Toshiaki Ishida, Isao Yokota, Kimikazu Matsumoto, Hiroyuki Shichino, Hiroyuki Fujisaki, Takeo Sarashina, Takehiko Kamijo, Tetsuya Takimoto, Tomoko Iehara and 2 more

Open access · goldAbstract read
In one paragraph

Article in Biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.8field-weighted citation impact, top 25% of its field
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

6 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Review
  3. Combination of clinical parameters andQuantitative imaging in medicine and surgery · 2025
    Article
  4. Article
  5. Article
  6. [Single-center application and analysis of neuroblastoma marker detection in childhood neuroblastoma].Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics
    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

12 authors at 10 institutions in 1 country.

Noriyuki NishimuraDepartment of Public Health, Graduate School of Health Science, Kobe University, Kobe 654-0142, Japan.ORCID 0000-0002-9000-4341
Toshiaki IshidaDepartment of Hematology/Oncology, Kobe Children's Hospital, Kobe 650-0047, Japan.ORCID 0000-0002-8327-1089
Isao YokotaDepartment of Biostatistics, Faculty of Medicine, Hokkaido University, Sapporo 060-0808, Japan.
Kimikazu MatsumotoChildren's Cancer Center, National Center for Child Health and Development, Tokyo 157-8535, Japan.
Hiroyuki ShichinoDepartment of Pediatrics, National Center for Global Health and Medicine, Tokyo 162-8655, Japan.
Hiroyuki FujisakiDepartment of Pediatric Hematology/Oncology, Osaka City General Hospital, Osaka 534-0021, Japan.
Takeo SarashinaDepartment of Pediatrics, Asahikawa Medical University, Asahikawa, 078-8510, Japan.
Takehiko KamijoResearch Institute for Clinical Oncology, Saitama Cancer Center, Saitama 362-0806, Japan.ORCID 0000-0003-4798-7546
Tetsuya TakimotoDepartment of Childhood Cancer Data Management, National Center for Child Health and Development, Tokyo 157-8535, Japan.
Tomoko IeharaDepartment of Pediatrics, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto 602-8566, Japan.
Tatsuro TajiriDepartment of Pediatric Surgery, Faculty of Medical Sciences, Kyushu University of Medicine, Fukuoka 812-8582, Japan.
On Behalf Of The Jccg Neuroblastoma Committee
National Center For Child Health and Development · JPAsahikawa Medical University · JPHokkaido University · JPKobe Children's Hospital · JPKobe University · JPKyoto Prefectural University of Medicine · JPKyushu University · JPNational Center for Global Health and Medicine · JPOsaka City General Hospital · JPSaitama Cancer Center · JP

Funding

Sysmex (Japan) N/A
6 · The paper itself

Abstract

High-risk neuroblastoma (HR-NB) patients remain far from obtaining optimal outcomes, with more than 50% relapse/regrowth rate despite current intensive multimodal therapy. This originated from the activation/proliferation of chemoresistant minimal residual disease (MRD). MRD with a significant prognostic was reported by several quantitative PCR (qPCR) or droplet digital PCR (ddPCR) assays quantitating different sets of NB-associated mRNAs (NB-mRNAs). The 7NB-mRNAs ddPCR assay quantitating CRMP1, DBH, DDC, GAP43, ISL1, PHOX2B, and TH mRNAs was reported to outperform other qPCR assays by a retrospective in-house observational study. In the present study, the Japan Children's Cancer Group (JCCG) Neuroblastoma Committee conducted a prospective multicenter observational study aimed at evaluating a prognostic value of MRD in bone marrow (BM-MRD) and peripheral blood (PB-MRD) detected by 7NB-mRNAs ddPCR assay. Between August 2018 and August 2022, 7 HR-NB patients who registered for JCCG clinical trials (JN-H-11 and JN-H-15) were enrolled. A total of 19 BM and 19 PB samples were collected, and 4/15 BM and 4/15 PB samples were classified as progressive disease (PD)/non-PD samples. BM-MRD and PB-MRD estimated area under curve (AUC) of 0.767 and 0.800 with a significant accuracy (AUC > 0.7). The present study validated a prognostic value of BM-MRD obtained by a previous study (AUC 0.723) and revealed the significant accuracy of PB-MRD as well as BM-MRD.

Indexed as

bone marrow (BM)droplet digital PCR (ddPCR)minimal residual disease (MRD)neuroblastoma-associated mRNAs (NB-mRNAs)neuroblastoma (NB)peripheral blood (PB)

Identifiers

PMID37887060
PMCPMC10604505
OpenAlexW4387822875

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.