Evidence map›Paper›PMID 30109673›Full record

ArticleJournal of neuro-oncology2018

Pediatric intracranial ependymoma: correlating signs and symptoms at recurrence with outcome in the second prospective AIEOP protocol follow-up.

Maura Massimino, Francesco Barretta, Piergiorgio Modena, Felice Giangaspero, Luisa Chiapparini, Alessandra Erbetta, Luna Boschetti, Manila Antonelli, Paolo Ferroli, Daniele Bertin and 26 more

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Article in Journal of neuro-oncology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

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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

36 authors.

Maura MassiminoPediatric Unit (MM, LB, VB, ES), Fondazione IRCCS Istituto Nazionale dei Tumori, Via Venezian 1, 20133, Milan, Italy. maura.massimino@istitutotumori.mi.it.ORCID http://orcid.org/0000-0002-5506-2001
Francesco BarrettaClinical Epidemiology and Trial Organization Unit (FB), Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Piergiorgio ModenaLaboratory of Genetics, Pathology Unit (PM), S. Anna General Hospital, Como, Italy.
Felice GiangasperoDepartment of Radiological, Oncological and Anatomo-Pathological Sciences (FG, MA), Sapienza University, Rome, Italy.
Luisa ChiappariniNeuroradiology (LC, AE), Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
Alessandra ErbettaNeuroradiology (LC, AE), Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
Luna BoschettiPediatric Unit (MM, LB, VB, ES), Fondazione IRCCS Istituto Nazionale dei Tumori, Via Venezian 1, 20133, Milan, Italy.
Manila AntonelliDepartment of Radiological, Oncological and Anatomo-Pathological Sciences (FG, MA), Sapienza University, Rome, Italy.
Paolo FerroliNeurosurgery Department (PF), Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
Daniele BertinPediatric Onco-Hematology (DB), A.O.U. Città della Salute e della Scienza, Turin, Italy.
Emilia PecoriPediatric Radiotherapy Unit (LG, EP), Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Veronica BiassoniPediatric Unit (MM, LB, VB, ES), Fondazione IRCCS Istituto Nazionale dei Tumori, Via Venezian 1, 20133, Milan, Italy.
Maria Luisa GarrèNeurosurgery Unit (MLG), Istituto Giannina Gaslini, Genoa, Italy.
Elisabetta SchiavelloPediatric Unit (MM, LB, VB, ES), Fondazione IRCCS Istituto Nazionale dei Tumori, Via Venezian 1, 20133, Milan, Italy.
Iacopo SardiNeuro-oncology (IS), Ospedale Pediatrico Meyer, Florence, Italy.
Elisabetta ViscardiPediatric Oncology Unit, (EV), Padova University, Padua, Italy.
Giovanni ScarzelloRadiotherapy Department (GS), IOV-IRCCS, Padua, Italy.
Maurizio MascarinPediatric Radiotherapy (MaM), CRO, Aviano, Italy.
Lucia QuagliettaPediatric Oncology (LQ), Ospedale Santobono-Pausillipon, Naples, Italy.
Giuseppe CinalliNeurosurgery Unit (GC), Ospedale Santobono-Pausillipon, Naples, Italy.
Lorenzo GenitoriNeurosurgery Unit (LG), Ospedale Pediatrico Meyer, Florence, Italy.
Paola PerettaPediatric Neurosurgery Unit (PP), A.O.U. Città della Salute e della Scienza, Turin, Italy.
Anna MussanoRadiotherapy (AM), A.O.U. Città della Salute e della Scienza, Turin, Italy.
Salvina BarraDepartment of Radiation Oncology (SB), IRCCS San Martino IST, Genoa, Italy.
Angela MastronuzziPediatric Hematology and Oncology Unit (AnM), Ospedale Pediatrico Bambino Gesù, Rome, Italy.
Carlo GiussaniNeurosurgery Unit (CG), University of Milano-Bicocca, Ospedale San Gerardo, Monza, Italy.
Carlo Efisio MarrasNeurosurgery Unit (CEM), Ospedale Pediatrico Bambino Gesù, Rome, Italy.
Rita BalterPediatric Oncology Unit (RB), Ospedale della Donna e del Bambino, Verona, Italy.
Patrizia BertoliniPediatric Oncology Unit (PB), University Hospital of Parma, Parma, Italy.
Assunta TorneselloPediatric Oncology Unit (AT), Ospedale Vito Fazzi, Lecce, Italy.
Milena La SpinaUnit of Paediatric Haematology and Oncology (MLS), Hospital Policlinico, University of Catania, Catania, Italy.
Francesca Romana ButtarelliNeurological Science (FRB), Sapienza University, Rome, Italy.
Antonio RuggieroPediatric Oncology (AR), Fondazione Policlinico Universitario Agostino Gemelli, Rome, Italy.
Massimo CaldarelliNeurosurgery (MC), Fondazione Policlinico Universitario Agostino Gemelli, Rome, Italy.
Geraldina PoggiAcquired Brain Lesions Unit (GP), IRCCS Eugenio Medea, Bosisio Parini, Italy.
Lorenza GandolaPediatric Radiotherapy Unit (LG, EP), Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe aims of patients' radiological surveillance are to: ascertain relapse; apply second-line therapy; accrue patients in phase 1/2 protocols if second-line therapy is not standardized/curative; and assess/treat iatrogenic effects. To lessen the emotional and socioeconomic burdens for patients and families, we ideally need to establish whether scheduled radiological surveillance gives patients a better outcome than waiting for symptoms and signs to appear.

methodsWe analyzed a prospective series of 160 newly-diagnosed and treated pediatric/adolescent patients with intracranial ependymoma, comparing patients with recurrent disease identified on scheduled MRI (the RECPT group; 34 cases) with those showing signs/symptoms of recurrent disease (the SYMPPT group; 16 cases). The median follow-up was 67 months.

resultsNo significant differences emerged between the two groups in terms of gender, age, tumor grade/site, shunting, residual disease, or type of relapse (local, distant, or concomitant). The time to relapse (median 19 months; range 5-104) and the MRI follow-up intervals did not differ between the SYMPPT and RECPT groups. The presence of signs/symptoms was an unfavorable factor for overall survival (OS) after recurrence (5-year OS: 8% vs. 37%, p = 0.001). On multivariable analysis, an adjusted model confirmed a significantly worse OS in the SYMPPT than in the RECPT patients.

conclusionsSymptomatic relapses carried a significantly worse survival for ependymoma patients than recurrences detected by MRI alone. It would therefore be desirable to identify recurrences before symptoms develop. Radiological follow-up should be retained in ependymoma patient surveillance because there is a chance of salvage treatment for relapses found on MRI.

Indexed as

AdolescentBrain NeoplasmsChildChild, PreschoolClinical ProtocolsEpendymomaFemaleFollow-Up StudiesHumansMagnetic Resonance ImagingMaleNeoplasm Recurrence, LocalPrognosisProspective StudiesChildhood ependymomaFollow-upRe-irradiationRelapseSurveillance

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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.