Evidence map›Paper›PMID 24342950›Full record

ArticleLeukemia2014

Next-generation sequencing and real-time quantitative PCR for minimal residual disease detection in B-cell disorders.

M Ladetto, M Brüggemann, L Monitillo, S Ferrero, F Pepin, D Drandi, D Barbero, A Palumbo, R Passera, M Boccadoro and 7 more

Registry-linked trialAbstract read
PubMed Publisher
In one paragraph

Article in Leukemia, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05218603 (A Prospective, Observational Study, to Evaluate the Maintenance With Bortezomib Plus Daratumumab), which is not on this map. Cited by 161 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
161citing papers in PubMed, 1 pooled it
23.8field-weighted citation impact, top 1% 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.

NCT05218603 unknown statusnot on this mapstarted 2021, after this paper: background citation

A Prospective, Observational Study, to Evaluate the Maintenance With Bortezomib Plus Daratumumab (V-Dara) After Induction With Bortezomib, Melphalan, Prednisone Plus Daratumumab (VMP-Dara) in Newly Diagnosed Multiple Myeloma (MM) Patients Non-eligible for Autologous Stem Cell Transplantation (ASCT): Alcyone-optimized Real World Evidence (RWE) Data

TypeobservationalSponsorPETHEMA FoundationRan2021 to 2025Enrolled100ConditionsMultiple Myeloma, Non-eligible for Autologous Stem Cell Transplantation (ASCT)ArmsBortezomib, Daratumumab
3 · Its place in the literature

Who cites it

161 citing papers in PubMed, 1 synthesis or guideline pooled it, 303 citations in OpenAlex.

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  9. Next-Generation Sequencing in Adult B Cell Acute Lymphoblastic Leukemia Patients.Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation · 2017
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101 more citing papers are in PubMed but not listed here.

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 5 institutions in 2 countries.

M LadettoDivision of Hematology, A.O. Azienda Ospedaliera Città della Salute e della Scienza di Torino, University of Torino, Torino, Italy.
M BrüggemannSecond Medical Department, University Hospital Schleswig-Holstein, Campus Kiel, Kiel, Germany.
L MonitilloDivision of Hematology, A.O. Azienda Ospedaliera Città della Salute e della Scienza di Torino, University of Torino, Torino, Italy.
S FerreroDivision of Hematology, A.O. Azienda Ospedaliera Città della Salute e della Scienza di Torino, University of Torino, Torino, Italy.
F PepinSequenta Inc, San Francisco, CA, USA.
D DrandiDivision of Hematology, A.O. Azienda Ospedaliera Città della Salute e della Scienza di Torino, University of Torino, Torino, Italy.
D BarberoDivision of Hematology, A.O. Azienda Ospedaliera Città della Salute e della Scienza di Torino, University of Torino, Torino, Italy.
A PalumboDivision of Hematology, A.O. Azienda Ospedaliera Città della Salute e della Scienza di Torino, University of Torino, Torino, Italy.
R PasseraDivision of Nuclear Medicine, Statistical Consultant, University of Torino, Torino, Italy.
M BoccadoroDivision of Hematology, A.O. Azienda Ospedaliera Città della Salute e della Scienza di Torino, University of Torino, Torino, Italy.
M RitgenSecond Medical Department, University Hospital Schleswig-Holstein, Campus Kiel, Kiel, Germany.
N GökbugetDepartment of Internal Medicine II, Hematology and Oncology, Goethe University Hospital, Frankfurt, Germany.
J ZhengSequenta Inc, San Francisco, CA, USA.
V CarltonSequenta Inc, San Francisco, CA, USA.
H TrautmannSecond Medical Department, University Hospital Schleswig-Holstein, Campus Kiel, Kiel, Germany.
M FahamSequenta Inc, San Francisco, CA, USA.
C PottSecond Medical Department, University Hospital Schleswig-Holstein, Campus Kiel, Kiel, Germany.
Azienda Ospedaliera Citta' della Salute e della Scienza di Torino · ITUniversity Hospital Schleswig-Holstein · DEUniversity of Lübeck · DEGoethe University Frankfurt · DEUniversity of Turin · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In this study, we compared immunoglobulin heavy-chain-gene-based minimal residual disease (MRD) detection by real-time quantitative PCR (RQ-PCR) and next-generation sequencing (NGS) to assess whether NGS could overcome some limitations of RQ-PCR and further increase sensitivity, specificity, accuracy and reproducibility. In total, 378 samples from 55 patients with acute lymphoblastic leukemia (ALL), mantle cell lymphoma (MCL) or multiple myeloma (MM) were investigated for clonotype identification, clonotype identity and comparability of MRD results. Forty-five clonotypes were identified by RQ-PCR and 49 by NGS. Clonotypes identified by both tools were identical or >97% homologous in 96% of cases. Both tools were able to routinely reach a sensitivity level of 1 × E-05. A good correlation of MRD results was observed (R=0.791, P<0.001), with excellent concordance in 79.6% of cases. Few discordant cases were observed across all disease subtypes. NGS showed at least the same level of sensitivity as allele-specific oligonucleotides-PCR, without the need for patient-specific reagents. We conclude that NGS is an effective tool for MRD monitoring in ALL, MCL and MM. Prospective comparative analysis of unselected cases is required to validate the clinical impact of NGS-based MRD assessment.

Indexed as

High-Throughput Nucleotide SequencingBiomarkers, TumorDNA, NeoplasmGene RearrangementGenes, ImmunoglobulinHumansLymphoma, Mantle-CellMultiple MyelomaNeoplasm, ResidualPrecursor Cell Lymphoblastic Leukemia-LymphomaProspective StudiesReal-Time Polymerase Chain ReactionTumor Cells, CulturedBiomarkers, TumorDNA, Neoplasm

Identifiers

PMID24342950
OpenAlexW1985012922

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.