Evidence map›Paper›PMID 30944610›Full record

ReviewOncology letters2019

Tumor infiltrating lymphocytes: The regulator of melanoma evolution.

Mihaela Antohe, Roxana Ioana Nedelcu, Luciana Nichita, Cristiana Gabriela Popp, Mirela Cioplea, Alice Brinzea, Anastasia Hodorogea, Andreea Calinescu, Mihaela Balaban, Daniela Adriana Ion and 5 more

Open access · diamondAbstract readReview
In one paragraph

Review in Oncology letters, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 71 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
71citing papers in PubMed, 1 pooled it
6.5field-weighted citation impact, top 3% 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

71 citing papers in PubMed, 1 synthesis or guideline pooled it, 93 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Advancements in Melanoma Therapies: From Surgery to Immunotherapy.Current treatment options in oncology · 2024
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Article
  16. Article
  17. Roadmap on Label-Free Super-Resolution Imaging.Laser & photonics reviews · 2023
    Article
  18. Article
  19. Review
  20. Article

11 more citing papers are in PubMed but not listed here.

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

15 authors at 5 institutions in 2 countries.

Mihaela AntoheDepartment of Pathophysiology, 'Carol Davila' University of Medicine and Pharmacy, 050474 Bucharest, Romania.
Roxana Ioana NedelcuDepartment of Pathophysiology, 'Carol Davila' University of Medicine and Pharmacy, 050474 Bucharest, Romania.
Luciana NichitaDepartment of Pathology, Colentina Clinical Hospital, 021103 Bucharest, Romania.
Cristiana Gabriela PoppDepartment of Pathology, Colentina Clinical Hospital, 021103 Bucharest, Romania.
Mirela CiopleaDepartment of Pathology, Colentina Clinical Hospital, 021103 Bucharest, Romania.
Alice BrinzeaDepartment of Pathophysiology, 'Carol Davila' University of Medicine and Pharmacy, 050474 Bucharest, Romania.
Anastasia HodorogeaDepartment of Pathophysiology, 'Carol Davila' University of Medicine and Pharmacy, 050474 Bucharest, Romania.
Andreea CalinescuDepartment of Dermatology, Colentina Clinical Hospital, 021103 Bucharest, Romania.
Mihaela BalabanDepartment of Dermatology, Derma 360° Clinic, 011274 Bucharest, Romania.
Daniela Adriana IonDepartment of Pathophysiology, 'Carol Davila' University of Medicine and Pharmacy, 050474 Bucharest, Romania.
Carmen DiaconuDepartment of Cellular and Molecular Pathology, 'Stefan S. Nicolau' Institute of Virology, 030304 Bucharest, Romania.
Coralia BleotuDepartment of Cellular and Molecular Pathology, 'Stefan S. Nicolau' Institute of Virology, 030304 Bucharest, Romania.
Daniel PiriciDepartment of Pathology, University of Medicine and Pharmacy of Craiova, 200349 Craiova, Romania.
Sabina Andrada ZuracDepartment of Pathology, Colentina Clinical Hospital, 021103 Bucharest, Romania.
Gabriela TurcuDepartment of Dermatology, Derma 360° Clinic, 011274 Bucharest, Romania.
Carol Davila University of Medicine and Pharmacy · ROSpitalul Clinic Colentina · ROClinical Emergency Hospital Bucharest · ROInstitute of Virology of the Slovak Academy of Sciences · SKUniversity of Medicine and Pharmacy of Craiova · RO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Melanoma is the most severe type of skin cancer and its incidence has increased in the last decades. In the United States, it is the 6th most common cancer in both men and women. Prognosis for patients with melanoma depends on the stage of the disease at the time of diagnosis and it can be influenced by the immunologic response. Melanoma has been historically considered an immunogenic malignancy. It often contains great amount of immune cells (different subsets of T-cells, dendritic cells, macrophages, neutrophils, mast cells, B lymphocytes), which may reflect a continuous intercommunication between host and tumor. It is not established if tumor-infiltrating lymphocytes (TILs) are induced by tumor cells or by other components of the microenvironment or when they are a host direct immunologic reaction. It has been observed that in many cases, the presence of a dense TIL is associated with good prognosis. The pattern and activation state of the cells which constitute TIL is variable and modulates the clinical outcome. An important step in the understanding of tumor immunobiology is the analysis of the populations and subsets of immune cells that form TIL. Besides its prognostic significance, after approval of cytotoxic T lymphocyte antigen 4, programmed cell death-1 and programmed death-1 ligand antibodies for the treatment of melanoma, the assessment of immune infiltrate composition has become even more captivating, as it could provide new target molecules and new biomarkers for predicting the effect of the treatment and disease outcome in patients treated with immunotherapy. In this review we discuss current state of knowledge in the field of immune cells that infiltrate melanoma, resuming the potential of TIL components to become prognostic markers for natural evolution, for response to drugs or valuable targets for new medication.

Indexed as

dendritic cellsimmunoeditingimmunogenic tumormelanoma

Identifiers

PMID30944610
PMCPMC6444298
OpenAlexW2908784791

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.