Evidence map›Paper›PMID 39682188›Full record

ReviewCancers2024

Into the Future: Fighting Melanoma with Immunity.

Derek A Corica, Scott D Bell, Peyton J Miller, Daniel T Kasperbauer, Nicholas J Lawler, Mark R Wakefield, Yujiang Fang

Abstract readReview
In one paragraph

Review in Cancers, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Review
  2. Article
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.

Derek A CoricaDepartment of Microbiology, Immunology & Pathology, Des Moines University, West Des Moines, IA 50266, USA.
Scott D BellDepartment of Microbiology, Immunology & Pathology, Des Moines University, West Des Moines, IA 50266, USA.
Peyton J MillerDepartment of Microbiology, Immunology & Pathology, Des Moines University, West Des Moines, IA 50266, USA.
Daniel T KasperbauerDepartment of Microbiology, Immunology & Pathology, Des Moines University, West Des Moines, IA 50266, USA.
Nicholas J LawlerDepartment of Microbiology, Immunology & Pathology, Des Moines University, West Des Moines, IA 50266, USA.
Mark R WakefieldDepartment of Surgery, University of Missouri School of Medicine, Columbia, MO 65212, USA.ORCID 0000-0003-2598-7895
Yujiang FangDepartment of Microbiology, Immunology & Pathology, Des Moines University, West Des Moines, IA 50266, USA.

Funding

Des Moines University 112-3119
6 · The paper itself

Abstract

Immunotherapy offers a novel and promising option in the treatment of late-stage melanoma. By utilizing the immune system to assist in tumor destruction, patients have additional options after tumor progression. Immune checkpoint inhibitors reduce the ability for tumors to evade the immune system by inhibiting key surface proteins used to inactivate T-cells. Without these surface proteins, T-cells can induce cytotoxic responses against tumors. Tumor infiltrating lymphocyte therapy is a form of adoptive cell therapy that takes advantage of a small subset of T-cells that recognize and infiltrate tumors. Isolation and rapid expansion of these colonies assist the immune system in mounting a charged response that can induce remission. Tumor vaccines deliver a high dose of unique antigens expressed by tumor cells to the entire body. The introduction of large quantities of tumor antigens upregulates antigen presenting cells and leads to effective activation of the immune system against tumors. Cytokine therapy introduces high amounts of chemical messengers that are endogenous to the immune system and support T-cell expansion. While other methods of immunotherapy exist, immune checkpoint inhibitors, tumor infiltrating lymphocytes, tumor vaccines, and cytokine therapy are commonly used to treat melanoma. Like many other cancer treatments, immunotherapy is not without adverse effects, as toxicities represent a major obstacle. However, immunotherapy has been efficacious in the treatment of melanoma.

Indexed as

melanomamelanoma immunotherapymelanoma treatment

Identifiers

PMID39682188
PMCPMC11640241

What OpenQuestion holds

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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.