Evidence map›Paper›PMID 35257217›Full record

ArticleActa neurochirurgica2022

Diagnosis, treatment, and outcome of primary CNS lymphoma-a single-center experience.

Joakim Wismann, Rune Hørlykke Sommer-Sørensen, Mikkel Seremet Kofoed, Bo Halle, Christian Bonde Pedersen, Mette Katrine Schulz, Mads Hjortdal Grønhøj, Thomas Stauffer Larsen, Michael Boe Møller, Frantz Rom Poulsen

Abstract read
PubMed Publisher
In one paragraph

Article in Acta neurochirurgica, 2022. 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
0.4field-weighted citation impact, top 40% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Conditional survival of elderly primary central nervous system lymphoma.Journal of cancer research and clinical oncology · 2023
    Article
  3. 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

10 authors at 1 institution in 1 country.

Joakim WismannDepartment of Neurosurgery, Odense University Hospital, Odense, Denmark. Joakim_wismann@hotmail.com.ORCID http://orcid.org/0000-0002-4658-9805
Rune Hørlykke Sommer-SørensenDepartment of Neurosurgery, Odense University Hospital, Odense, Denmark.
Mikkel Seremet KofoedDepartment of Neurosurgery, Odense University Hospital, Odense, Denmark.ORCID http://orcid.org/0000-0002-6819-4345
Bo HalleDepartment of Neurosurgery, Odense University Hospital, Odense, Denmark.
Christian Bonde PedersenDepartment of Neurosurgery, Odense University Hospital, Odense, Denmark.
Mette Katrine SchulzDepartment of Neurosurgery, Odense University Hospital, Odense, Denmark.
Mads Hjortdal GrønhøjDepartment of Neurosurgery, Odense University Hospital, Odense, Denmark.
Thomas Stauffer LarsenDepartment of Clinical Research, University of Southern Denmark, Odense, Denmark.ORCID http://orcid.org/0000-0002-8418-6708
Michael Boe MøllerDepartment of Clinical Research, University of Southern Denmark, Odense, Denmark.ORCID http://orcid.org/0000-0003-2041-3630
Frantz Rom PoulsenDepartment of Neurosurgery, Odense University Hospital, Odense, Denmark.ORCID http://orcid.org/0000-0001-5715-6901
University of Southern Denmark · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPrimary CNS lymphoma (PCNSL) is a highly aggressive non-Hodgkin lymphoma (NHL) that occurs in the CNS (e.g. brain, meninges, spinal cord, cerebrospinal fluid, or intraocular involvement) in the absence of systemic NHL. Tumor resection does not improve survival, and neurosurgical intervention is generally limited to stereotactic biopsy to provide a histopathological diagnosis.

objectiveThe objective of this single-center study was to evaluate the management and outcome of PCNSL patients diagnosed by biopsy, using overall survival and progression-free survival as endpoints.

methodsAt our department of neurosurgery, 140 patients were diagnosed with PCNSL by biopsy between January 1, 2009, and December 31, 2018. Of these, 37 patients were included in the study and were divided into three groups according to their postoperative therapy.

resultsMedian OS was 35.7 months for the intensive treatment group, 29.5 months for the moderate treatment group, and 8.6 months for the palliative treatment group. The intensive and moderate treatment groups had similar progression-free survival, while the palliative treatment group had poor overall and progression-free survival. Six patients were long-term survivors (> 80 months). Age under 65 years was the main significant parameter affecting overall survival.

conclusionIn this cohort, patients with PCNSL had an overall fair prognosis if they (1) were under 65 years old, (2) had a performance score < 2 at the time of diagnosis, and (3) received either intensive or moderate chemotherapeutic treatment. Biopsy is still the primary diagnostic tool; other methods have been investigated but are not yet recommended.

Indexed as

Central Nervous System NeoplasmsLymphoma, Non-HodgkinAgedBrainCohort StudiesHumansNeurosurgical ProceduresPrognosisProgression-Free SurvivalRetrospective StudiesTreatment OutcomeBrain biopsyOverall survivalPCNSLProgression-free survival

Identifiers

PMID35257217
OpenAlexW4220759955

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.