Evidence map›Paper›PMID 21768298›Full record

ArticleBlood2011

Follicular lymphoma in situ: clinical implications and comparisons with partial involvement by follicular lymphoma.

Armin G Jegalian, Franziska C Eberle, Svetlana D Pack, Mariya Mirvis, Mark Raffeld, Stefania Pittaluga, Elaine S Jaffe

Abstract readComparative Study
In one paragraph

Article in Blood, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
11.3field-weighted citation impact, top 1% 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

52 citing papers in PubMed, 159 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Splenosis involved by in situ follicular B-cell neoplasm.Virchows Archiv : an international journal of pathology · 2025
    Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Follicular lymphoma and marginal zone lymphoma: how many diseases?Virchows Archiv : an international journal of pathology · 2023
    Review
  11. Precursory or early lesions of follicular lymphoma: clinical features, pathology, and genetics.Journal of clinical and experimental hematopathology : JCEH · 2023
    Review
  12. Follicular lymphoma: updates for pathologists.Journal of pathology and translational medicine · 2022
    Review
  13. Review
  14. Genetic evolution ofHaematologica · 2021
    Article
  15. Article
  16. Article
  17. Review
  18. Review
  19. Review
  20. Review
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.

Armin G JegalianNational Cancer Institute, Bethesda, MD, USA.
Franziska C Eberle
Svetlana D Pack
Mariya Mirvis
Mark Raffeld
Stefania Pittaluga
Elaine S Jaffe
National Cancer Institute · US

Funding

Molecular Diagnostics Core LaboratoryZICBC011079 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI XI, LIQIANG · 2009 to 2025
$33.8M
Lymphoma Disease Discovery and DefintionZIASC000550 · NCI · DIVISION OF CLINICAL SCIENCES - NCI · PI JAFFE, ELAINE · 2009 to 2025
$16.9M
Hematopathology FellowshipZIEBC011241 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI JAFFE, ELAINE · 2009 to 2025
$11.1M
Immunohistochemistry Core LaboratoryZICBC011087 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI RAFFELD, MARK · 2009 to 2015
$7.4M
Development of FISH Molecular Diagnostics to support Clinical Trials at NCIZIDBC011349 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI PACK, SVETLANA · 2010 to 2014
$2.7M
Intramural NIH HHS
6 · The paper itself

Abstract

Follicular lymphoma in situ (FLIS) was first described nearly a decade ago, but its clinical significance remains uncertain. We reevaluated our original series and more recently diagnosed cases to develop criteria for the distinction of FLIS from partial involvement by follicular lymphoma (PFL). A total of 34 cases of FLIS were identified, most often as an incidental finding in a reactive lymph node. Six of 34 patients had prior or concurrent FL, and 5 of 34 had FLIS composite with another lymphoma. Of patients with negative staging at diagnosis and available follow-up (21 patients), only one (5%) developed FL (follow-up: median, 41 months; range, 10-118 months). Follow-up was not available in 2 cases. Fluorescence in situ hybridization for BCL2 gene rearrangement was positive in all 17 cases tested. PFL patients were more likely to develop FL, diagnosed in 9 of 17 (53%) who were untreated. Six patients with PFL were treated with local radiation therapy (4) or rituximab (2) and remained with no evidence of disease. FLIS can be reliably distinguished from PFL and has a very low rate of progression to clinically significant FL. FLIS may represent the tissue counterpart of circulating t(14;18)-positive B cells.

Indexed as

AdultAgedChromosomes, Human, Pair 14Chromosomes, Human, Pair 18Cohort StudiesDiagnosis, DifferentialFemaleFollow-Up StudiesHumansLymphoma, FollicularMaleMiddle AgedMutationNeoplasm StagingProto-Oncogene Proteins c-bcl-2Translocation, GeneticProto-Oncogene Proteins c-bcl-2

Identifiers

PMID21768298
PMCPMC3175777
OpenAlexW2035580412

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.