Evidence map›Paper›PMID 27567676›Full record

ArticleJournal of experimental & clinical cancer research : CR2016

Brain stereotactic biopsy flow cytometry for central nervous system lymphoma characterization: advantages and pitfalls.

Iole Cordone, Serena Masi, Mariantonia Carosi, Antonello Vidiri, Francesco Marchesi, Mirella Marino, Stefano Telera, Alessia Pasquale, Andrea Mengarelli, Laura Conti and 3 more

Open access · goldAbstract readComparative Study
In one paragraph

Article in Journal of experimental & clinical cancer research : CR, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

12 citing papers in PubMed, 26 citations in OpenAlex.

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  10. Long-term in vivo microscopy of CAR T cell dynamics during eradication of CNS lymphoma in mice.Proceedings of the National Academy of Sciences of the United States of America · 2019
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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

13 authors at 1 institution in 1 country.

Iole CordoneClinical Pathology, Regina Elena National Cancer Institute, Rome, Italy.
Serena MasiClinical Pathology, Regina Elena National Cancer Institute, Rome, Italy.
Mariantonia CarosiPathology, Regina Elena National Cancer Institute, Rome, Italy.
Antonello VidiriRadiology, Regina Elena National Cancer Institute, Rome, Italy.
Francesco MarchesiHematology and Stem Cell Transplant, Regina Elena National Cancer Institute, Rome, Italy.
Mirella MarinoPathology, Regina Elena National Cancer Institute, Rome, Italy.
Stefano TeleraNeurosurgery, Regina Elena National Cancer Institute, Rome, Italy.
Alessia PasqualeClinical Pathology, Regina Elena National Cancer Institute, Rome, Italy.
Andrea MengarelliHematology and Stem Cell Transplant, Regina Elena National Cancer Institute, Rome, Italy.
Laura ContiClinical Pathology, Regina Elena National Cancer Institute, Rome, Italy.
Edoardo PescarmonaPathology, Regina Elena National Cancer Institute, Rome, Italy.
Andrea PaceNeuroncology, Regina Elena National Cancer Institute, Rome, Italy.
Carmine M CarapellaNeurosurgery, Regina Elena National Cancer Institute, Rome, Italy. carmine.carapella@ifo.gov.it.
National Cancer Institute · MY

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBrain stereotactic biopsy (SB) followed by conventional histopathology and immunohistochemistry (IHC) is the gold standard approach for primary central nervous system lymphoma (PCNSL) diagnosis. Flow cytometry (FCM) characterization of fine-needle aspiration cytology and core needle biopsies are increasingly utilized to diagnose lymphomas however, no biological data have been published on FCM characterization of fresh single cell suspension from PCNSL SB. The aim of this study was to establish the feasibility and utility of FCM for the diagnosis and characterization of brain lymphomas from a tissue samples obtained by a single SB disaggregation.

methodsTwenty-nine patients with a magnetic resonance suggestive for PCNSL entered the study. A median of 6 SB were performed for each patient. A cell suspension generated from manual tissue disaggregation of a single, unfixed, brain SB, was characterized by FCM. The FCM versus standard approach was prospectively compared.

resultsFCM and IHC showed an high degree of agreement (89 %) in brain lymphoma identification. By FCM, 16 out of 18 PCNSL were identified within 2 h from biopsy. All were of B cell type, with a heterogeneous CD20 mean fluorescence intensity (MFI), CD10 positive in 3 cases (19 %) with surface Ig light chain restriction documented in 11 cases (69 %). No false positive lymphomas cases were observed. Up to 38 % of the brain leukocyte population consisted of CD8 reactive T cells, in contrast with the CD4 positive lymphocytes of the peripheral blood samples (P < 0.001). By histopathology, 18 B-PCNSL, only one CD10 positive (5 %), 1 primitive neuroectodermal tumor (PNET) and 10 gliomas were diagnosed. A median of 6 days was required for IHC diagnosis.

conclusionComplementary to histopathology FCM can contribute to a better characterization of PCNSL, although necrosis and previous steroid treatment can represent a pitfall of this approach. A single brain SB is a valid source for accurate FCM characterization of both lymphoma and reactive lymphocyte population, routinely applicable for antigen intensity quantification and consistently documenting an active mechanism of reactive CD8 T-lymphocytes migration in brain lymphomas. Moreover, FCM confirmed to be more sensitive than IHC for the identification of selected markers.

Indexed as

AdolescentAdultAgedAged, 80 and overBiopsy, Fine-NeedleBiopsy, Large-Core NeedleBrain NeoplasmsFemaleFlow CytometryGliomaHumansLymphomaMaleMiddle AgedNeuroectodermal TumorsProspective StudiesBrain stereotactic biopsyFlow cytometryPCNSLTumor side population

Identifiers

PMID27567676
PMCPMC5002320
OpenAlexW2514083167

What OpenQuestion holds

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LicenceCC BY
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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.