Evidence map›Paper›PMID 30104292›Full record

ArticleThe oncologist2018

Durable Response to Nivolumab in a Pediatric Patient with Refractory Glioblastoma and Constitutional Biallelic Mismatch Repair Deficiency.

Musa AlHarbi, Nahla Ali Mobark, Latifa AlMubarak, Rasha Aljelaify, Mariam AlSaeed, Amal Almutairi, Fatmah Alqubaishi, M Emarat Hussain, Ali Abdullah O Balbaid, Amal Said Marie and 5 more

Open access · bronzeAbstract readCase Reports
In one paragraph

Article in The oncologist, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed, 4 pooled it
7.0field-weighted citation impact, top 2% 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

45 citing papers in PubMed, 4 syntheses or guidelines pooled it, 70 citations in OpenAlex.

  1. Pooled it
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  17. Article
  18. Hereditary cancer syndromes.World journal of clinical oncology · 2023
    Review
  19. Molecular and Circulating Biomarkers in Patients with Glioblastoma.International journal of molecular sciences · 2022
    Review
  20. Article
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

15 authors at 6 institutions in 2 countries.

Musa AlHarbiDepartment of Oncology, Comprehensive Cancer Centre, King Fahad Medical City, Riyadh, Saudi Arabia.
Nahla Ali MobarkDepartment of Oncology, Comprehensive Cancer Centre, King Fahad Medical City, Riyadh, Saudi Arabia.
Latifa AlMubarakGenomics Research Department, Saudi Human Genome Project, King Fahad Medical City and King Abdulaziz City for Science and Technology, Riyadh, Saudi Arabia.
Rasha AljelaifyGenomics Research Department, Saudi Human Genome Project, King Fahad Medical City and King Abdulaziz City for Science and Technology, Riyadh, Saudi Arabia.
Mariam AlSaeedGenomics Research Department, Saudi Human Genome Project, King Fahad Medical City and King Abdulaziz City for Science and Technology, Riyadh, Saudi Arabia.
Amal AlmutairiGenomics Research Department, Saudi Human Genome Project, King Fahad Medical City and King Abdulaziz City for Science and Technology, Riyadh, Saudi Arabia.
Fatmah AlqubaishiGenomics Research Department, Saudi Human Genome Project, King Fahad Medical City and King Abdulaziz City for Science and Technology, Riyadh, Saudi Arabia.
M Emarat HussainRadiology Department, King Fahad Medical City, Riyadh, Saudi Arabia.
Ali Abdullah O BalbaidGenomics Research Department, Saudi Human Genome Project, King Fahad Medical City and King Abdulaziz City for Science and Technology, Riyadh, Saudi Arabia.
Amal Said MarieDepartment of Radiation Oncology, Comprehensive Cancer Centre, King Fahad Medical City, Riyadh, Saudi Arabia.
Lamia AlSubaieDivision of Genetics, Department of Pediatric, King Abdulaziz Medical City, Riyadh, Saudi Arabia.
Saeed AlShiebanDepartment of Pathology, King Abdulaziz Medical City, National Guard Health Affair, Riyadh, Saudi Arabia.
Nada alTassanGenetics Department, King Faisal Specialists Hospital and Research Center, Riyadh, Saudi Arabia.
Shakti H RamkissoonWake Forest Comprehensive Cancer Center and Department of Pathology, Winston-Salem, North Carolina, USA.
Malak AbedalthagafiGenomics Research Department, Saudi Human Genome Project, King Fahad Medical City and King Abdulaziz City for Science and Technology, Riyadh, Saudi Arabia malthagafi@kfmc.med.sa.
King Abdulaziz City for Science and Technology · SAKing Fahd Medical City · SAKing Abdulaziz Medical City · SABrigham and Women's Hospital · USFoundation Medicine (United States)King Faisal Specialist Hospital & Research Centre · SA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Primary brain tumors are a leading cause of cancer-related morbidity and mortality in children. Glioblastoma (GBM) is a high-grade astrocytoma that occurs in both children and adults and is associated with a poor prognosis. Despite extensive study in recent years, the clinical management of these tumors has remained largely unchanged, consisting of surgical resection, conventional chemotherapy, and radiotherapy. Although the etiology and genomic drivers in GBM are diverse, constitutional mismatch repair-deficiency (CMMRD) syndrome is a rare, recessively inherited disease with a predisposition to gliomagenesis. CMMRD results from biallelic mutations in one of the mismatch repair genes including mutL homolog 1 (

Indexed as

Antineoplastic Agents, ImmunologicalBrain NeoplasmsChild, PreschoolDNA Mismatch RepairDNA Repair EnzymesFemaleGlioblastomaHumansNivolumabAntineoplastic Agents, ImmunologicalDNA Repair EnzymesNivolumab

Identifiers

PMID30104292
PMCPMC6292541
OpenAlexW2886443268

What OpenQuestion 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 OpenQuestion graph.