Evidence map›Paper›PMID 41696493›Full record

ArticleNeuro-oncology advances

Evaluation of sex differences in survival among glioblastoma patients treated with immune checkpoint inhibitors.

Vihang Nakhate, Catharina Westergaard, Zhou Lan, Aleksandra B Lasica, Alona Muzikansky, Brooke Barlow, Alyssa Russ, Loai Aker, Albert Jiao, Ian Pan and 16 more

Abstract read
In one paragraph

Article in Neuro-oncology advances. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Review
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

26 authors.

Vihang NakhateCenter for Neuro-Oncology, Dana-Farber Cancer Institute, Boston.ORCID https://orcid.org/0000-0002-2941-9740
Catharina WestergaardCenter for Neuro-Oncology, Dana-Farber Cancer Institute, Boston.
Zhou LanHarvard Medical School, Boston.
Aleksandra B LasicaCenter for Neuro-Oncology, Dana-Farber Cancer Institute, Boston.ORCID https://orcid.org/0000-0002-9739-5103
Alona MuzikanskyBiostatistics Center, Massachusetts General Hospital, Boston.ORCID https://orcid.org/0000-0001-7585-8181
Brooke BarlowCenter for Neuro-Oncology, Dana-Farber Cancer Institute, Boston.
Alyssa RussCenter for Neuro-Oncology, Dana-Farber Cancer Institute, Boston.
Loai AkerHarvard Medical School, Boston.
Albert JiaoHarvard Medical School, Boston.
Ian PanHarvard Medical School, Boston.
Thomas A NelsonDivision of Neuro-Oncology, Department of Neurosurgery, University of California San Francisco, San Francisco.
Chibueze D NwagwuHarvard Medical School, Boston.
Elisa AquilantiCenter for Neuro-Oncology, Dana-Farber Cancer Institute, Boston.ORCID https://orcid.org/0000-0002-1343-5017
Tracy T BatchelorCenter for Neuro-Oncology, Dana-Farber Cancer Institute, Boston.
Rameen BeroukhimCenter for Neuro-Oncology, Dana-Farber Cancer Institute, Boston.
Tamar R BergerCenter for Neuro-Oncology, Dana-Farber Cancer Institute, Boston.
Ugonma ChukwuekeCenter for Neuro-Oncology, Dana-Farber Cancer Institute, Boston.ORCID https://orcid.org/0000-0003-0598-9535
L Nicolas Gonzalez CastroCenter for Neuro-Oncology, Dana-Farber Cancer Institute, Boston.ORCID https://orcid.org/0000-0001-7699-5188
Eudocia Quant LeeCenter for Neuro-Oncology, Dana-Farber Cancer Institute, Boston.
J Ricardo Mcfaline-FigueroaBrain & Spine Tumor Center, Perlmutter Cancer Center, NYU Langone Health, New York.
Lakshmi NayakCenter for Neuro-Oncology, Dana-Farber Cancer Institute, Boston.ORCID https://orcid.org/0000-0003-2725-8717
John Y RheeCenter for Neuro-Oncology, Dana-Farber Cancer Institute, Boston.
David A ReardonCenter for Neuro-Oncology, Dana-Farber Cancer Institute, Boston.
Raymond Y HuangHarvard Medical School, Boston.
Patrick Y WenCenter for Neuro-Oncology, Dana-Farber Cancer Institute, Boston.ORCID https://orcid.org/0000-0002-0774-7700
Gilbert YoussefCenter for Neuro-Oncology, Dana-Farber Cancer Institute, Boston.ORCID https://orcid.org/0000-0001-6109-7692

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Sex differences in glioblastoma (GBM) are recognized, but their treatment implications remain unclear. Recent preclinical studies have characterized mechanisms of sex-biased anti-tumor immunity in GBM, and have found in murine models that males derive greater survival benefit from immune checkpoint inhibitor (ICI). We evaluated sex differences associated with ICI in GBM patients. Methods: We retrospectively evaluated consecutive patients with newly diagnosed GBM (nGBM) or recurrent GBM (rGBM) treated with ICI on clinical trials at one institution from 2014 to 2022. Progression-free survival (PFS) and overall survival (OS) were evaluated by Kaplan-Meier analysis, univariate and multivariable regression models. Sex-by-treatment interactions were assessed relative to a concurrent reference group treated on non-ICI clinical trials. Results: 296 patients with nGBM (58% male, 19% ICI) and 458 patients with rGBM (60% male, 40% ICI) were evaluated. In nGBM, ICI was not associated with sex difference in PFS (HR Conclusion: In nGBM and rGBM, ICI therapy was not associated with sex difference in PFS or OS. Clinically meaningful sex-based outcome differences may be better understood by prospective evaluation in clinical trials.

Indexed as

glioblastomaimmune checkpoint inhibitorsimmunotherapysex differences

Identifiers

PMID41696493
PMCPMC12901605

What OpenQuestion holds

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LicenceCC BY
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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.