Evidence map›Paper›PMID 40134851›Full record

ArticleNeuro-oncology advances

Phase 1 trial of hypofractionated stereotactic re-irradiation in combination with nivolumab, ipilimumab, and bevacizumab for recurrent high-grade gliomas.

Solmaz Sahebjam, Raju R Raval, Peter A Forsyth, Heiko Enderling, Nam D Tran, John A Arrington, Robert Macaulay, Haley K Perlow, Joshua D Palmer, Jayeeta Ghose and 11 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 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. 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

21 authors.

Solmaz SahebjamJohns Hopkins University School of Medicine, The Sidney Kimmel Cancer Center, Sibley Memorial Hospital, Washington, DC, USA.ORCID https://orcid.org/0000-0001-9930-9937
Raju R RavalPelotonia Institute for Immuno-Oncology, Columbus, Ohio, USA.
Peter A ForsythH. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida, USA.
Heiko EnderlingThe University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Nam D TranH. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida, USA.
John A ArringtonH. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida, USA.
Robert MacaulayH. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida, USA.
Haley K PerlowDepartment of Radiation Oncology, University Hospitals Seidman Cancer Center, Case Western Reserve University, Cleveland, Ohio, USA.
Joshua D PalmerThe Ohio State University Wexner Medical Center, James Cancer Hospital, Columbus, OH, USA.
Jayeeta GhoseThe Ohio State University Wexner Medical Center, James Cancer Hospital, Columbus, OH, USA.
Prajwal RajappaPelotonia Institute for Immuno-Oncology, Columbus, Ohio, USA.
Pierre GiglioThe Ohio State University Wexner Medical Center, James Cancer Hospital, Columbus, OH, USA.ORCID https://orcid.org/0000-0001-5165-0984
Zihai LiPelotonia Institute for Immuno-Oncology, Columbus, Ohio, USA.ORCID https://orcid.org/0000-0003-4603-927X
Arnold B EtameH. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida, USA.
Sepideh MokhtariH. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida, USA.
Ruben J Cruz-ChamorroH. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida, USA.
Menal BhandariH. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida, USA.
Ram ThapaH. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida, USA.
Timothy J RobinsonYale School of Medicine, Smilow Cancer Center, New Haven, Connecticut, USA.
Dung-Tsa ChenH. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida, USA.ORCID https://orcid.org/0000-0001-5026-415X
Hsiang-Hsuan Michael YuH. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Our previous clinical investigation suggested that hypofractionated stereotactic re-irradiation (HFSRT) and PD-1 blockade may act synergistically to enhance the immune response against glioma. This subsequent trial investigated the dual blockade of CTLA4 and PD-1 in combination with HFSRT and bevacizumab. Methods: This phase I study enrolled eligible patients with bevacizumab-naïve recurrent glioblastoma or anaplastic astrocytoma. Participants received nivolumab, ipilimumab, and bevacizumab concurrently with HFSRT (3000 cGy in 5 fractions). Subsequently, nivolumab, ipilimumab, and bevacizumab were administered for a total of 4 cycles followed by nivolumab and bevacizumab until progression. The primary end point of this study was the safety and tolerability of HFSRT in combination with nivolumab, ipilimumab, and bevacizumab in patients with recurrent HGGs. Secondary end points included 6-month survival and 9-month survival. Results: Twenty-six patients were treated. Treatment-related adverse events (TRAEs) of grade 3 or 4 were observed in 12 (48%) evaluable patients with no unexpected TRAEs. Six months and 9 months survival were 92% (95% CI, 82-100%) and 75% (95% CI, 60-95%), respectively. The median progression-free survival and overall survival were 7.1 months (95% CI, 5.2-12.2) and 15.6 months (95% CI, 11.3-27.0), respectively. Conclusions: The combination of HFSRT with ipilimumab, nivolumab, and bevacizumab is safe. Our results underscore the potential synergies between stereotactic re-irradiation and checkpoint immunotherapy in patients with recurrent high-grade gliomas.

Indexed as

glioblastomahigh-grade gliomaipilimumabnivolumabstereotactic re-irradiation

Identifiers

PMID40134851
PMCPMC11934552

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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.