Evidence map›Paper›PMID 41160229›Full record

ArticleJournal of neuro-oncology2025

Clinical, toxicity and long-term neurocognitive outcomes of first-line intensive chemotherapy in infant medulloblastoma: a single-center cohort study following AIEOP recommendations.

Giada Del Baldo, Valentina Di Ruscio, Antonella Cacchione, Annalisa Lo Sasso, Ludovica Corvino, Claudia D'Orazio, Andrea De Salvo, Giulia Albino, Selene Cipri, Evelina Miele and 6 more

Abstract read
In one paragraph

Article in Journal of neuro-oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

16 authors.

Giada Del BaldoHematology/Oncology, Cell Therapy, Gene Therapies, and Hemopoietic Transplant, Bambino Gesù Children's Hospital, IRCCS, Piazza S. Onofrio 4, 00165, Rome, Italy.ORCID http://orcid.org/0000-0003-3540-4331
Valentina Di RuscioHematology/Oncology, Cell Therapy, Gene Therapies, and Hemopoietic Transplant, Bambino Gesù Children's Hospital, IRCCS, Piazza S. Onofrio 4, 00165, Rome, Italy.ORCID http://orcid.org/0000-0002-9581-2751
Antonella CacchioneHematology/Oncology, Cell Therapy, Gene Therapies, and Hemopoietic Transplant, Bambino Gesù Children's Hospital, IRCCS, Piazza S. Onofrio 4, 00165, Rome, Italy.ORCID http://orcid.org/0000-0003-4901-9952
Annalisa Lo SassoDepartment of Medicine DAME-Division of Pediatrics, University of Udine, Udine, Italy.
Ludovica CorvinoUniCamillus - Saint Camillus International University of Health Sciences, Rome, Italy.
Claudia D'OrazioImaging Department, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.ORCID http://orcid.org/0000-0002-0264-8519
Andrea De SalvoHematology/Oncology, Cell Therapy, Gene Therapies, and Hemopoietic Transplant, Bambino Gesù Children's Hospital, IRCCS, Piazza S. Onofrio 4, 00165, Rome, Italy.ORCID http://orcid.org/0000-0002-8520-8008
Giulia AlbinoHematology/Oncology, Cell Therapy, Gene Therapies, and Hemopoietic Transplant, Bambino Gesù Children's Hospital, IRCCS, Piazza S. Onofrio 4, 00165, Rome, Italy.ORCID http://orcid.org/0009-0001-6266-0966
Selene CipriHematology/Oncology, Cell Therapy, Gene Therapies, and Hemopoietic Transplant, Bambino Gesù Children's Hospital, IRCCS, Piazza S. Onofrio 4, 00165, Rome, Italy.ORCID http://orcid.org/0000-0002-8730-0094
Evelina MieleHematology/Oncology, Cell Therapy, Gene Therapies, and Hemopoietic Transplant, Bambino Gesù Children's Hospital, IRCCS, Piazza S. Onofrio 4, 00165, Rome, Italy.ORCID http://orcid.org/0000-0002-4747-1032
Isabella GiovannoniPathology Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.ORCID http://orcid.org/0000-0002-9980-6594
Sabrina RossiPathology Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.ORCID http://orcid.org/0000-0002-1477-8855
Giovanna Stefania ColafatiImaging Department, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.ORCID http://orcid.org/0000-0002-1142-4904
Sabina VennariniPediatric Radiotherapy Unit, Fondazione Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Istituto Nazionale dei Tumori, Milan, Italy.ORCID http://orcid.org/0000-0002-8712-8781
Andrea CaraiNeurosurgery Unit, Neurosciences, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.ORCID http://orcid.org/0000-0002-5203-7855
Angela MastronuzziHematology/Oncology, Cell Therapy, Gene Therapies, and Hemopoietic Transplant, Bambino Gesù Children's Hospital, IRCCS, Piazza S. Onofrio 4, 00165, Rome, Italy. angela.mastronuzzi@opbg.net.ORCID http://orcid.org/0000-0002-4408-2373

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe long-term neurocognitive impact of craniospinal irradiation (CSI) in young children with medulloblastoma (MB) has driven the development of alternative strategies aimed at improving survival while delaying or avoiding CSI.

methodsWe retrospectively analyzed a cohort of patients under 5 years of age with MB treated at Bambino Gesù Children's Hospital between 2007 and 2023 with intensive chemotherapy regimens according to AIEOP recommendation. Clinical, radiological, histopathological, molecular, neurocognitive, and toxicity data were collected.

resultsAmong 42 patients under 5 years, 25 met inclusion criteria (median age 25.3 months, range 5.0-51.3). Histology included classic (52%), desmoplastic/nodular (20%), extensive nodularity (16%), and large cell/anaplastic (12%). SHH was the most common molecular subgroup (52%), followed by Group 3 (32%) and Group 4 (16%). At a median follow-up of 95.7 months, 68% were alive in complete remission. Two- and 5-year overall survival (OS) were 80.0% (95%CI: 58.4-91.1) and 65.9% (95%CI: 42.8-81.4); progression-free survival (PFS) was 68.0% (95%CI: 46.1-82.5) and 63.8% (95%CI: 41.8-79.2). Survival differed by risk group: low-risk patients achieved 100% OS and PFS, standard-risk intermediate, high-risk lowest. All experienced grade 3-4 hematological toxicity; late endocrine effects occurred in four patients, no other long-term toxicities reported. median IQ was stable from diagnosis (885.3) to last follow-up (8392.5.4).

conclusionOur retrospective study of infants MB treated with first-line intensive chemotherapy shows encouraging survival rates. Importantly, neurocognitive function was preserved over time, supporting radiation-sparing strategies, and toxicity was manageable in all cases.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsCerebellar NeoplasmsMedulloblastomaChild, PreschoolFemaleFollow-Up StudiesHumansInfantMaleRetrospective StudiesSurvival RateIntensive chemotherapyMedulloblastomaNeurocognitive outcomeRadiation-sparing strategiesSurvivalYoung children

Identifiers

PMID41160229
PMCPMC12572033

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