Evidence map›Paper›PMID 28423678›Full record

ArticleOncotarget2017

Influence of ipilimumab on expanded tumour derived T cells from patients with metastatic melanoma.

Jon Bjoern, Rikke Lyngaa, Rikke Andersen, Lisbet Rosenkrantz Hölmich, Sine Reker Hadrup, Marco Donia, Inge Marie Svane

Erratum issuedOpen access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 14% 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

25 citing papers in PubMed, 1 synthesis or guideline pooled it, 31 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Tumor-Infiltrating Lymphocyte Therapy in Melanoma: Facts to the Future.Clinical cancer research : an official journal of the American Association for Cancer Research · 2023
    Review
  9. Review
  10. Review
  11. Article
  12. Nanobodies Enhancing Cancer Visualization, Diagnosis and Therapeutics.International journal of molecular sciences · 2021
    Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. A Multi-center Phase I Trial of Ipilimumab in Patients with Myelodysplastic Syndromes following Hypomethylating Agent Failure.Clinical cancer research : an official journal of the American Association for Cancer Research · 2018
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

Jon BjoernCenter for Cancer Immune Therapy, Herlev Hospital, University of Copenhagen, Copenhagen, Denmark.
Rikke LyngaaSection for Immunology and Vaccinology, Technical University of Denmark, Copenhagen, Denmark.
Rikke AndersenCenter for Cancer Immune Therapy, Herlev Hospital, University of Copenhagen, Copenhagen, Denmark.
Lisbet Rosenkrantz HölmichDepartment of Plastic Surgery, Herlev Hospital, University of Copenhagen, Copenhagen, Denmark.
Sine Reker HadrupSection for Immunology and Vaccinology, Technical University of Denmark, Copenhagen, Denmark.
Marco DoniaCenter for Cancer Immune Therapy, Herlev Hospital, University of Copenhagen, Copenhagen, Denmark.
Inge Marie SvaneCenter for Cancer Immune Therapy, Herlev Hospital, University of Copenhagen, Copenhagen, Denmark.
University of Copenhagen · DKHerlev Hospital · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionTumour infiltrating lymphocyte (TIL) based adoptive cell therapy (ACT) is a promising treatment for patients with advanced melanoma. Retrospective studies suggested an association between previous treatment with anti-CTLA-4 antibodies and long term survival after subsequent ACT. Thus, we hypothesized that treatment with anti-CTLA-4 antibodies can induce favourable changes to be detected in TILs.

resultsExpanded T cells from Ipilimumab treated patients had a higher proportion of cells expressing CD27, intracellular CTLA-4, TIM-3 and LAG-3. In addition, broader and more frequent T cell responses against common tumour antigens were detected in patients treated with Ipilimumab as compared to anti-CTLA-4 naïve patients. MATERIALS AND

methodsExpanded TILs were obtained from patients with advanced melanoma who had received Ipilimumab in the previous six months, or had not received any type of anti-CTLA-4 antibody. T cell specificity and expression of phenotypic and exhaustion markers were scrutinized as well as functional properties.

conclusionsIpilimumab may induce tumor-infiltration of T cells of a more naïve phenotype expressing markers related to activation or exhaustion. Additionally, Ipilimumab may increase the frequency of T cells recognizing common tumour associated antigens.

Indexed as

AdultAgedAntineoplastic Agents, ImmunologicalAntineoplastic Combined Chemotherapy ProtocolsBiomarkersCTLA-4 AntigenFemaleHumansImmunomodulationIpilimumabLymphocyte ActivationLymphocytes, Tumor-InfiltratingMaleMelanomaMiddle AgedNeoplasm GradingAntineoplastic Agents, ImmunologicalBiomarkersCTLA-4 AntigenCTLA4 protein, humanIpilimumabCTLA-4immunotherapyipilimumabmelanomatumour infiltrating lymphocyte

Identifiers

PMID28423678
PMCPMC5432318
OpenAlexW2593804207

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.