Evidence map›Paper›PMID 38342925›Full record

ReviewJournal of experimental & clinical cancer research : CR2024

From glioma gloom to immune bloom: unveiling novel immunotherapeutic paradigms-a review.

Moksada Regmi, Yingjie Wang, Weihai Liu, Yuwei Dai, Shikun Liu, Ke Ma, Guozhong Lin, Jun Yang, Hongyi Liu, Jian Wu and 1 more

Abstract readReview
In one paragraph

Review in Journal of experimental & clinical cancer research : CR, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing 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

20 citing papers in PubMed.

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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

11 authors.

Moksada RegmiDepartment of Neurosurgery, Peking University Third Hospital, Peking University, Beijing, 100191, China.
Yingjie WangDepartment of Neurosurgery, Peking University Third Hospital, Peking University, Beijing, 100191, China.
Weihai LiuDepartment of Neurosurgery, Peking University Third Hospital, Peking University, Beijing, 100191, China.
Yuwei DaiDepartment of Neurosurgery, Peking University Third Hospital, Peking University, Beijing, 100191, China.
Shikun LiuDepartment of Neurosurgery, Peking University Third Hospital, Peking University, Beijing, 100191, China.
Ke MaPeking University Health Science Center, Beijing, 100191, China.
Guozhong LinDepartment of Neurosurgery, Peking University Third Hospital, Peking University, Beijing, 100191, China.
Jun YangDepartment of Neurosurgery, Peking University Third Hospital, Peking University, Beijing, 100191, China.
Hongyi LiuHenan Academy of Innovations in Medical Science (AIMS), Zhengzhou, 450003, China.
Jian WuHenan Academy of Innovations in Medical Science (AIMS), Zhengzhou, 450003, China. karena.wu@foxmail.com.
Chenlong YangDepartment of Neurosurgery, Peking University Third Hospital, Peking University, Beijing, 100191, China. vik.yang@pku.edu.cn.ORCID http://orcid.org/0000-0001-8102-8811

Funding

AO Spine Research Start-up Grant AOS-Startup-21-016Beijing Natural Science Foundation 7222217Beijing Nova Program 20230484356Capital Health Research and Development of Special 2022-4-40918National Natural Science Foundation of China 82371319Peking University Clinical Medicine Plus X-Young Scholars Project PKU2021LCXQ007Peking University Third Hospital Clinical Key Project BYSYZD2021023
6 · The paper itself

Abstract

In tumor therapeutics, the transition from conventional cytotoxic drugs to targeted molecular therapies, such as those targeting receptor tyrosine kinases, has been pivotal. Despite this progress, the clinical outcomes have remained modest, with glioblastoma patients' median survival stagnating at less than 15 months. This underscores the urgent need for more specialized treatment strategies. Our review delves into the progression toward immunomodulation in glioma treatment. We dissect critical discoveries in immunotherapy, such as spotlighting the instrumental role of tumor-associated macrophages, which account for approximately half of the immune cells in the glioma microenvironment, and myeloid-derived suppressor cells. The complex interplay between tumor cells and the immune microenvironment has been explored, revealing novel therapeutic targets. The uniqueness of our review is its exhaustive approach, synthesizing current research to elucidate the intricate roles of various molecules and receptors within the glioma microenvironment. This comprehensive synthesis not only maps the current landscape but also provides a blueprint for refining immunotherapy for glioma, signifying a paradigm shift toward leveraging immune mechanisms for improved patient prognosis.

Indexed as

Brain NeoplasmsGlioblastomaGliomaMyeloid-Derived Suppressor CellsHumansImmunomodulationImmunotherapyTumor MicroenvironmentGliomasImmune checkpointsImmunotherapyInhibitors

Identifiers

PMID38342925
PMCPMC10860318

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.