Evidence map›Paper›PMID 41788986›Full record

ArticleFrontiers in oncology2026

Targeted and systemic therapies for recurrent adult ependymomas: real-world outcomes from a single institution and concise literature review.

Marta Maccari, Alberto Bosio, Mario Caccese, Marta Padovan, Angela Guerriero, Giovanni Librizzi, Giovanna Pintacuda, Luisa Bellu, Alba Fiorentino, Francesco Volpin and 5 more

Abstract read
In one paragraph

Article in Frontiers in oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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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

15 authors.

Marta MaccariDepartment of Surgery, Oncology and Gastroenterology, University of Padova, Padova, Italy.
Alberto BosioDepartment of Surgery, Oncology and Gastroenterology, University of Padova, Padova, Italy.
Mario CacceseMedical Oncology 1, Veneto Institute of Oncology IOV-IRCCS, Padova, Italy.
Marta PadovanMedical Oncology 1, Veneto Institute of Oncology IOV-IRCCS, Padova, Italy.
Angela GuerrieroDepartment of Surgical Pathology Unit, Padova University Hospital, Padova, Italy.
Giovanni LibrizziPadova Neuroscience Center (PNC), University of Padova, Padova, Italy.
Giovanna PintacudaRadiology Unit, Veneto Institute of Oncology IOV-IRCCS, Padova, Italy.
Luisa BelluRadiotherapy Unit, IOV-IRCCS Veneto Institute of Oncology, Padova, Italy.
Alba FiorentinoDepartment of Radiation Oncology, General Regional Hospital F. Miulli, (BA), Acquaviva delle Fonti, Italy.
Francesco VolpinDivision of Neurosurgery, Padova University Hospital, Padova, Italy.
Tamara IusAcademic Neurosurgery, Department of Neurosciences, University of Padova, Padova, Italy.
Franco ChioffiDivision of Neurosurgery, Padova University Hospital, Padova, Italy.
Luca DenaroAcademic Neurosurgery, Department of Neurosciences, University of Padova, Padova, Italy.
Sara LonardiMedical Oncology 1, Veneto Institute of Oncology IOV-IRCCS, Padova, Italy.
Giuseppe LombardiMedical Oncology 1, Veneto Institute of Oncology IOV-IRCCS, Padova, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Recurrent adult ependymomas lack standard systemic therapies and evidence on chemotherapy and targeted agents is limited. This study aimed to retrospectively evaluated outcomes of systemic therapies, including targeted combinations, in a real-world cohort. Methods: Adult patients with intracranial or spinal ependymoma treated at our institution between 2013 and 2025 who received at least one systemic line at recurrence were included. Tumor response was assessed according to RANO criteria. Primary endpoints were disease control rate (DCR) and progression-free survival (PFS). Secondary endpoints were overall survival from the start of the first line treatment (OSt) and overall survival from diagnosis (OS). Results: Among 47 patients, 12 received systemic therapy at recurrence. The median follow up duration for the entire cohort was 28.3 months. Temozolomide (TMZ) was the most commonly used agent (n=12). TMZ monotherapy achieved a DCR of 57% with 6- and 12-month PFS rates of 85.7% and 57.1%, respectively. Targeted therapy was administered to 7 patients: the TMZ-Lapatinib combination provided limited benefit (DCR 33%, median PFS 2.9 months), bevacizumab-based regimens showed variable efficacy; bevacizumab alone achieved a DCR of 33% with one case of prolonged stabilization (>58 months), while bevacizumab plus fotemustine yielded a PFS of 14.1 months. Treatments were generally well tolerated, with limited grade 3 toxicities. Sequential systemic therapy, up to five lines, was feasible in selected cases. Median OSt was not reached; 12-month OS was 66.7%. Conclusions: This real-world analysis indicates that temozolomide is feasible and associated with disease stabilization in selected patients, while bevacizumab-based combinations showed signals of clinical activity in recurrent adult ependymomas. Prospective, biomarker-driven multicenter trials are warranted to optimize systemic strategies in this rare disease.

Indexed as

bevacizumabchemotherapyependymomastargeted therapytemozolomide

Identifiers

PMID41788986
PMCPMC12956718

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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.