Evidence map›Paper›PMID 42750913›Full record

ReviewNeuro-oncology practice2026

Multidisciplinary recommendations for routine follow-up of isocitrate dehydrogenase‑mutant glioma in 2026: Adapting clinical practice to the molecular era.

Mary Jane Lim-Fat, Amelie Darlix, Bogdana Suchorska, Antonella Castellano, Giuseppe Minniti, Maarten Wijnenga, Susan C Short, Martin J van den Bent

Abstract readReview
In one paragraph

Review in Neuro-oncology practice, 2026. 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

8 authors.

Mary Jane Lim-FatDivision of Neurology, Department of Medicine, Sunnybrook Health Sciences Centre, Toronto, Canada.ORCID https://orcid.org/0000-0002-4317-5770
Amelie DarlixDepartment of Medical Oncology, Institut Régional du Cancer de Montpellier, University of Montpellier, Montpellier, France.ORCID https://orcid.org/0000-0003-1384-1709
Bogdana SuchorskaDepartment of Neurosurgery, Heidelberg University Hospital, Heidelberg, Germany.ORCID https://orcid.org/0000-0002-1083-8232
Antonella CastellanoDepartment of Radiotherapy, Vita-Salute San Raffaele University, Milan, Italy.ORCID https://orcid.org/0000-0002-4137-9016
Giuseppe MinnitiDepartment of Radiological Sciences, Oncology and Anatomical Pathology, Sapienza University of Rome, Rome, Italy.ORCID https://orcid.org/0000-0003-1239-1603
Maarten WijnengaBrain Tumor Center at Erasmus MC Cancer Institute, Rotterdam, the Netherlands.ORCID https://orcid.org/0000-0002-2690-5022
Susan C ShortDepartment of Radiotherapy, Leeds Institute of Medical Research, St James's Hospital, Leeds, UK.ORCID https://orcid.org/0000-0003-4423-7256
Martin J van den BentBrain Tumor Center at Erasmus MC Cancer Institute, Rotterdam, the Netherlands.ORCID https://orcid.org/0000-0001-5710-5127

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Grade 2 and most grade 3 isocitrate dehydrogenase (IDH) mutant diffuse gliomas are slow growing tumors, for which however no curative treatment is available. Although surgery as extensive as possible improves outcome, for virtually all patients at some point in time further treatment is necessary. Treatment with radiotherapy and chemotherapy is very effective in controlling tumor growth in most patients, but has side effects. Therefore, in many patients these are postponed and a postoperative "watch-and-wait" observational strategy is followed. With the approval of IDH inhibitors, another effective strategy has emerged allowing further delay of treatment with radiotherapy and chemotherapy. This underscores the need for guidance how to best follow these patients during their subsequent phases of treatment, but most guidelines give only minimal recommendations for follow-up. Follow-up should not be limited to imaging only, but should also routinely assess seizures and cognition of patients. Follow-up intervals should be based on the risk of progression, allowing longer intervals for patients with oligodendroglioma, for more definitively treated patients and for patients with longer lasting disease stabilization. Evidence justifying a more intensive follow-up of patients on IDH inhibitors than for patients on a "watch-and-wait" strategy is lacking. Assessing a growth trajectory over time and routine two-dimensional or three-dimensional tumor assessment will allow identification of early changes in growth rate. This manuscript provides guidance for optimal follow-up of these patients with perspectives from all involved disciplines, as indeed the follow-up of these patients needs to be truly multidisciplinary, at every step along the pathway of these patients.

Identifiers

PMID42750913
PMCPMC13578488

What OpenQuestion holds

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Registered trials

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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.