Evidence map›Paper›PMID 29804159›Full record

ArticleNeuroradiology2018

Is deep brain involvement in intracranial primary central nervous system lymphoma of importance for penetration of chemotherapeutic agents?

Torstein R Meling, Anna Latysheva, Michele Da Broi, Guro Jahr, Harald Holte, Klaus Beiske, Kyrre Eeg Emblem

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Article in Neuroradiology, 2018. 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
0.5field-weighted citation impact, top 33% 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

2 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
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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 1 institution in 1 country.

Torstein R MelingDepartment of Neurosurgery, Oslo University Hospital, 0027, Oslo, Norway. torsteinrmeling@gmail.com.ORCID http://orcid.org/0000-0001-6595-0873
Anna LatyshevaDepartment of Radiology, Oslo University Hospital, Oslo, Norway.
Michele Da BroiDepartment of Neurosurgery, Oslo University Hospital, 0027, Oslo, Norway.
Guro JahrDepartment of Neurosurgery, Oslo University Hospital, 0027, Oslo, Norway.
Harald HolteDepartment of Oncology, Oslo University Hospital, Oslo, Norway.
Klaus BeiskeFaculty of Medicine, Institute of Clinical Medicine, University of Oslo, Oslo, Norway.
Kyrre Eeg EmblemDepartment of Diagnostic Physics, Oslo University Hospital, Oslo, Norway.
Oslo University Hospital · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe purposes of this study are to study the impact of deep brain involvement on overall survival (OS) and progression-free survival (PFS) in intracranial primary CNS lymphoma (PCNSL), and to explore possible mechanisms for this impact using advanced MRI techniques.

methodsSeventy-nine patients with histologically verified PCNSL were identified from a prospective clinical database of patients treated at Oslo University Hospital between 2003 and 2014. Patients were treated per standard chemotherapeutic regimens (N = 57) or no chemotherapy (N = 22). Anatomical MRIs were available in all patients to assess tumor load and location based on contrast agent enhancement visible on T1-weighted images. Diffusion MRIs were available in 33 (42%) patients and perfusion MRI in 13 (16%) patients that received active treatment.

resultsAcross all patients, OS and PFS were 16.4 and 9.8 months, respectively. In multivariate analysis, MRI-based deep brain involvement (80%) was the only negative significant factor of OS (OR = 14.2; P < 0.005). While a reduced Karnofsky performance status was associated with deep brain involvement (P < 0.05), neither chemotherapy regimen, neurologic status, nor patient age were independent significant factors for OS or PFS in this setting. Compared to other tumors and healthy tissue levels, MRI perfusion showed more pathologic hemodynamic flow signatures in tumors with deep brain involvement.

conclusionIn intracranial PCNSL, the only significant prognostic factor for OS and PFS in multivariate analysis was age and deep brain involvement. While contingent on a small study sample, we hypothesize this may in part be explained by regional differences in vascular supply and delivery from a dysfunctional perfusion signature.

Indexed as

AdolescentAdultAgedAged, 80 and overCentral Nervous System NeoplasmsContrast MediaFemaleHumansLymphomaMagnetic Resonance ImagingMaleMiddle AgedNorwayPrognosisProspective StudiesSurvival RateContrast MediaLymphomaMRIOncologyPrognostic factorsSurgery

Identifiers

PMID29804159
OpenAlexW2803408409

What OpenQuestion holds

Textmetadata
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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.