Evidence map›Paper›PMID 25802883›Full record

ArticleMolecular genetics & genomic medicine2015

Personalized treatment of Sézary syndrome by targeting a novel CTLA4:CD28 fusion.

Aleksandar Sekulic, Winnie S Liang, Waibhav Tembe, Tyler Izatt, Semyon Kruglyak, Jeffrey A Kiefer, Lori Cuyugan, Victoria Zismann, Christophe Legendre, Mark R Pittelkow and 6 more

Open access · goldAbstract read
In one paragraph

Article in Molecular genetics & genomic medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed, 1 pooled it
7.4field-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

53 citing papers in PubMed, 1 synthesis or guideline pooled it, 85 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. TCR Pathway Mutations in Mature T Cell Lymphomas.Journal of immunology (Baltimore, Md. : 1950) · 2023
    Review
  9. Review
  10. Review
  11. Review
  12. Review
  13. Frontiers in immunology · 2023
    Article
  14. Article
  15. Review
  16. Article
  17. Review
  18. Genetic Landscape of Peripheral T-Cell Lymphoma.Life (Basel, Switzerland) · 2022
    Review
  19. Mice transgenic for humanOncoimmunology · 2022
    Article
  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

16 authors at 4 institutions in 1 country.

Aleksandar SekulicMayo Clinic Scottsdale, Arizona ; Translational Genomics Research Institute Phoenix, Arizona.
Winnie S LiangTranslational Genomics Research Institute Phoenix, Arizona.
Waibhav TembeTranslational Genomics Research Institute Phoenix, Arizona.
Tyler IzattTranslational Genomics Research Institute Phoenix, Arizona.
Semyon KruglyakIllumina Inc. San Diego, California.
Jeffrey A KieferTranslational Genomics Research Institute Phoenix, Arizona.
Lori CuyuganTranslational Genomics Research Institute Phoenix, Arizona.
Victoria ZismannTranslational Genomics Research Institute Phoenix, Arizona.
Christophe LegendreTranslational Genomics Research Institute Phoenix, Arizona.
Mark R PittelkowMayo Clinic Scottsdale, Arizona.
John J GohmannLexington Oncology Associates Lexington, Kentucky.
Fernando R De CastroDermatology Associates of Kentucky Lexington, Kentucky.
Jeffrey TrentTranslational Genomics Research Institute Phoenix, Arizona.
John CarptenTranslational Genomics Research Institute Phoenix, Arizona.
David W CraigTranslational Genomics Research Institute Phoenix, Arizona.
Timothy K McDanielDerby Lane Farm Versailles, Kentucky.
Translational Genomics Research Institute · USCentral Kentucky Research Associates · USIllumina (United States) · USMayo Clinic in Arizona · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Matching molecularly targeted therapies with cancer subtype-specific gene mutations is revolutionizing oncology care. However, for rare cancers this approach is problematic due to the often poor understanding of the disease's natural history and phenotypic heterogeneity, making treatment of these cancers a particularly unmet medical need in clinical oncology. Advanced Sézary syndrome (SS), an aggressive, exceedingly rare variant of cutaneous T-cell lymphoma (CTCL) is a prototypical example of a rare cancer. Through whole genome and RNA sequencing (RNA-seq) of a SS patient's tumor we discovered a highly expressed gene fusion between CTLA4 (cytotoxic T lymphocyte antigen 4) and CD28 (cluster of differentiation 28), predicting a novel stimulatory molecule on the surface of tumor T cells. Treatment with the CTLA4 inhibitor ipilimumab resulted in a rapid clinical response. Our findings suggest a novel driver mechanism for SS, and cancer in general, and exemplify an emerging model of cancer treatment using exploratory genomic analysis to identify a personally targeted treatment option when conventional therapies are exhausted.

Indexed as

CD28CTLA4Sézary syndrome

Identifiers

PMID25802883
PMCPMC4367085
OpenAlexW2052811491

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.