Evidence map›Paper›PMID 34328587›Full record

ReviewCurrent treatment options in oncology2021

Immunosuppression in Medulloblastoma: Insights into Cancer Immunity and Immunotherapy.

Zahraa F Audi, Zahraa Saker, Mahdi Rizk, Hayat Harati, Youssef Fares, Hisham F Bahmad, Sanaa M Nabha

Abstract readReview
PubMed Publisher
In one paragraph

Review in Current treatment options in oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.8field-weighted citation impact, top 15% of its field
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

13 citing papers in PubMed, 20 citations in OpenAlex.

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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

7 authors at 2 institutions in 2 countries.

Zahraa F Audi *Neuroscience Research Center, Faculty of Medical Sciences, Lebanese University, Beirut, Lebanon.
Zahraa Saker *Neuroscience Research Center, Faculty of Medical Sciences, Lebanese University, Beirut, Lebanon.
Mahdi Rizk *Neuroscience Research Center, Faculty of Medical Sciences, Lebanese University, Beirut, Lebanon.
Hayat HaratiNeuroscience Research Center, Faculty of Medical Sciences, Lebanese University, Beirut, Lebanon.
Youssef FaresNeuroscience Research Center, Faculty of Medical Sciences, Lebanese University, Beirut, Lebanon.
Hisham F Bahmad *Arkadi M. Rywlin M.D. Department of Pathology and Laboratory Medicine, Mount Sinai Medical Center, 4300 Alton Rd, Miami Beach, FL, USA. Hisham.Bahmad@msmc.com.ORCID 0000-0003-3799-2595
Sanaa M Nabha *Neuroscience Research Center, Faculty of Medical Sciences, Lebanese University, Beirut, Lebanon. snabha@ul.edu.lb.
Lebanese University · LBMount Sinai Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

opinion statementMedulloblastoma (MB) is the most common pediatric brain malignancy, with a 5-year overall survival (OS) rate of around 65%. The conventional MB treatment, comprising surgical resection followed by irradiation and adjuvant chemotherapy, often leads to impairment in normal body functions and poor quality of life, especially with the increased risk of recurrence and subsequent development of secondary malignancies. The development and progression of MB are facilitated by a variety of immune-evading mechanisms such as the secretion of immunosuppressive molecules, activation of immunosuppressive cells, inhibition of immune checkpoint molecules, impairment of adhesive molecules, downregulation of the major histocompatibility complex (MHC) molecules, protection against apoptosis, and activation of immunosuppressive pathways. Understanding the tumor-immune relationship in MB is crucial for effective development of immune-based therapeutic strategies. In this comprehensive review, we discuss the immunological aspect of the brain, focusing on the current knowledge tackling the mechanisms of MB immune suppression and evasion. We also highlight several key immunotherapeutic approaches developed to date for the treatment of MB.

Indexed as

Immune ToleranceBiomarkersBrainCerebellar NeoplasmsClinical Decision-MakingCombined Modality TherapyDisease ManagementDisease SusceptibilityHumansImmunocompromised HostImmunotherapyMedulloblastomaOrgan SpecificityTreatment OutcomeTumor MicroenvironmentBiomarkersBrain tumor,Clinical trialImmunosuppression,Immunotherapy,Medulloblastoma,

Identifiers

PMID34328587
OpenAlexW3183144877

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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 Socratic graph.