Evidence map›Paper›PMID 36276741›Full record

ArticleHeliyon2022

Minimal residual disease detected by droplet digital PCR in peripheral blood stem cell grafts has a prognostic impact on high-risk neuroblastoma patients.

Nanako Nino, Toshiaki Ishida, Naoko Nakatani, Kyaw San Lin, Kaung Htet Nay Win, Cho Yee Mon, Akihiro Nishimura, Shotaro Inoue, Akihiro Tamura, Nobuyuki Yamamoto and 7 more

Open access · goldAbstract read
In one paragraph

Article in Heliyon, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.2field-weighted citation impact, top 43% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Review
  3. 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

17 authors at 2 institutions in 1 country.

Nanako NinoDepartment of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Japan.
Toshiaki IshidaDepartment of Hematology and Oncology, Kobe Children's Hospital, Kobe, Japan.
Naoko NakataniDepartment of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Japan.
Kyaw San LinDepartment of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Japan.
Kaung Htet Nay WinDepartment of Public Health, Kobe University Graduate School of Health Science, Kobe, Japan.
Cho Yee MonDepartment of Public Health, Kobe University Graduate School of Health Science, Kobe, Japan.
Akihiro NishimuraDepartment of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Japan.
Shotaro InoueDepartment of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Japan.
Akihiro TamuraDepartment of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Japan.
Nobuyuki YamamotoDepartment of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Japan.
Suguru UemuraDepartment of Hematology and Oncology, Kobe Children's Hospital, Kobe, Japan.
Atsuro SaitoDepartment of Hematology and Oncology, Kobe Children's Hospital, Kobe, Japan.
Takeshi MoriDepartment of Hematology and Oncology, Kobe Children's Hospital, Kobe, Japan.
Daiichiro HasegawaDepartment of Hematology and Oncology, Kobe Children's Hospital, Kobe, Japan.
Yoshiyuki KosakaDepartment of Hematology and Oncology, Kobe Children's Hospital, Kobe, Japan.
Kandai NozuDepartment of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Japan.
Noriyuki NishimuraDepartment of Public Health, Kobe University Graduate School of Health Science, Kobe, Japan.
Kobe University · JPKobe Children's Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

More than half of high-risk neuroblastoma (NB) patients have experienced relapse due to the activation of chemoresistant minimal residual disease (MRD) even though they are treated by high-dose chemotherapy with autologous peripheral blood stem cell (PBSC) transplantation. Although MRD in high-risk NB patients can be evaluated by quantitative PCR with several sets of neuroblastoma-associated mRNAs (NB-mRNAs), the prognostic significance of MRD in PBSC grafts (PBSC-MRD) is unclear. In the present study, we collected 20 PBSC grafts from 20 high-risk NB patients and evaluated PBSC-MRD detected by droplet digital PCR (ddPCR) with 7NB-mRNAs (CRMP1, DBH, DDC, GAP43, ISL1, PHOX2B, and TH mRNA). PBSC-MRD in 11 relapsed patients was significantly higher than that in 9 non-relapsed patients. Patients with a higher PBSC-MRD had a lower 3-year event-free survival (P = 0.0148). The present study suggests that PBSC-MRD detected by ddPCR with 7NB-mRNAs has a prognostic impact on high-risk NB patients.

Indexed as

Droplet digital PCR (ddPCR)Minimal residual disease (MRD)Neuroblastoma-associated mRNAs (NB-mRNAs)Neuroblastoma (NB)Peripheral blood stem cell (PBSC)

Identifiers

PMID36276741
PMCPMC9578974
OpenAlexW4303684664

What OpenQuestion holds

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LicenceCC BY
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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.