Evidence map›Paper›PMID 31575060›Full record

ArticleCancers2019

Exosomal microRNAs from Longitudinal Liquid Biopsies for the Prediction of Response to Induction Chemotherapy in High-Risk Neuroblastoma Patients: A Proof of Concept SIOPEN Study.

Martina Morini, Davide Cangelosi, Daniela Segalerba, Danilo Marimpietri, Federica Raggi, Aurora Castellano, Doriana Fruci, Jaime Font de Mora, Adela Cañete, Yania Yáñez and 15 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed, 2 pooled it
2.3field-weighted citation impact, top 11% 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

40 citing papers in PubMed, 2 syntheses or guidelines pooled it, 55 citations in OpenAlex.

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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

25 authors at 7 institutions in 5 countries.

Martina MoriniLaboratorio di Biologia Molecolare, IRCCS Istituto Giannina Gaslini, 16147 Genova, Italy. martinamorini@gaslini.org.
Davide CangelosiLaboratorio di Biologia Molecolare, IRCCS Istituto Giannina Gaslini, 16147 Genova, Italy.
Daniela SegalerbaLaboratorio di Biologia Molecolare, IRCCS Istituto Giannina Gaslini, 16147 Genova, Italy.
Danilo MarimpietriU.O.C. Laboratorio di Cellule Staminali Post Natali e Terapie Cellulari, IRCCS Istituto Giannina Gaslini, 16147 Genova, Italy.
Federica RaggiLaboratorio di Biologia Molecolare, IRCCS Istituto Giannina Gaslini, 16147 Genova, Italy.
Aurora CastellanoDipartimento di Oncoematologia, Ospedale Pediatrico Bambino Gesù IRCCS, 00165 Roma, Italy.
Doriana FruciDipartimento di Oncoematologia, Ospedale Pediatrico Bambino Gesù IRCCS, 00165 Roma, Italy.
Jaime Font de MoraHospital Universitario y Politècnico La Fe, 46026 Valencia, Spain.
Adela CañeteHospital Universitario y Politècnico La Fe, 46026 Valencia, Spain.
Yania YáñezHospital Universitario y Politècnico La Fe, 46026 Valencia, Spain.
Virginie VipreyLeeds Institute of Medical Research at St James's University Hospital, LS9 7TF Leeds, UK.
Maria Valeria CorriasLaboratorio Terapie Sperimentali in Oncologia, IRCCS Istituto Giannina Gaslini, 16147 Genova, Italy.
Barbara CarliniAnatomia Patologica, IRCCS Istituto Giannina Gaslini, 16147 Genova, Italy.
Annalisa PezzoloU.O.C. Laboratorio di Cellule Staminali Post Natali e Terapie Cellulari, IRCCS Istituto Giannina Gaslini, 16147 Genova, Italy.
Gudrun SchleiermacherCurie Institute, 75248 Paris, France.
Katia MazzoccoAnatomia Patologica, IRCCS Istituto Giannina Gaslini, 16147 Genova, Italy.
Ruth LadensteinSt Anna Children's Hospital, 1090 Wien, Austria.
Angela Rita SementaAnatomia Patologica, IRCCS Istituto Giannina Gaslini, 16147 Genova, Italy.
Massimo ConteOncoematologia Pediatrica, IRCCS Istituto Giannina Gaslini, 16147 Genova, Italy.
Alberto GaraventaOncoematologia Pediatrica, IRCCS Istituto Giannina Gaslini, 16147 Genova, Italy.
Susan BurchillLeeds Institute of Medical Research at St James's University Hospital, LS9 7TF Leeds, UK.
Roberto LukschFondazione IRCSS Istituto Nazionale dei Tumori, 20133 Milano, Italy.
Maria Carla BoscoLaboratorio di Biologia Molecolare, IRCCS Istituto Giannina Gaslini, 16147 Genova, Italy. mariacarlabosco@gaslini.org.
Alessandra EvaLaboratorio di Biologia Molecolare, IRCCS Istituto Giannina Gaslini, 16147 Genova, Italy.
Luigi VaresioLaboratorio di Biologia Molecolare, IRCCS Istituto Giannina Gaslini, 16147 Genova, Italy.
Istituto Giannina Gaslini · ITHospital Universitari i Politècnic La Fe · ESBambino Gesù Children's Hospital · ITSt James's University Hospital · GBFondazione IRCCS Istituto Nazionale dei Tumori · ITInstitut Curie · FRSt Anna Children's Hospital · AT

Funding

Associazione Italiana per la Lotta al Neuroblastoma noneAssociazione Italiana per la Ricerca sul Cancro 17459Ministero della Salute none
6 · The paper itself

Abstract

Despite intensive treatment, 50% of children with high-risk neuroblastoma (HR-NB) succumb to their disease. Progression through current trials evaluating the efficacy of new treatments for children with HR disease usually depends on an inadequate response to induction chemotherapy, assessed using imaging modalities. In this study, we sought to identify circulating biomarkers that might be detected in a simple blood sample to predict patient response to induction chemotherapy. Since exosomes released by tumor cells can drive tumor growth and chemoresistance, we tested the hypothesis that exosomal microRNA (exo-miRNAs) in blood might predict response to induction chemotherapy. The exo-miRNAs expression profile in plasma samples collected from children treated in HR-NBL-1/SIOPEN before and after induction chemotherapy was compared to identify a three exo-miRs signature that could discriminate between poor and good responders. Exo-miRNAs expression also provided a chemoresistance index predicting the good or poor prognosis of HR-NB patients.

Indexed as

chemotherapy responseexosomesliquid biopsymiRNAneuroblastoma

Identifiers

PMID31575060
PMCPMC6826693
OpenAlexW2975612929

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.