Evidence map›Paper›PMID 39456853›Full record

ReviewInternational journal of molecular sciences2024

Advancing Treatment Options for Merkel Cell Carcinoma: A Review of Tumor-Targeted Therapies.

Helena M Nammour, Karla Madrigal, Caroline T Starling, Hung Q Doan

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Review
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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

4 authors.

Helena M NammourUTHealth McGovern Medical School, Houston, TX 77030, USA.ORCID 0009-0000-5531-7636
Karla MadrigalUTHealth McGovern Medical School, Houston, TX 77030, USA.ORCID 0009-0009-1872-9741
Caroline T StarlingDepartment of Dermatology, UTHealth McGovern Medical School, Houston, TX 77030, USA.ORCID 0000-0003-4540-9363
Hung Q DoanDepartment of Dermatology, UTHealth McGovern Medical School, Houston, TX 77030, USA.ORCID 0000-0002-4715-0562

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although rare, Merkel cell carcinoma (MCC) is a highly aggressive and increasingly prevalent neuroendocrine cancer of the skin. While current interventions, including surgical resection, radiation, and immunotherapy have been employed in treating many patients, those who remain unresponsive to treatment are met with sparse alternatives and a grim prognosis. For this reason, it is of interest to expand the repertoire of available therapies for MCC patients who remain resistant to current primary interventions. Recently, our improved mechanistic understanding of aberrant cell signaling observed in both MCPyV-positive and -negative MCC has facilitated exploration into several small molecules and inhibitors, among them receptor tyrosine kinase inhibitors (TKIs) and somatostatin analogs (SSAs), both of which have positively improved response rates and reduced tumor volumes upon application to treatment of MCC. The introduction of such targeted therapies into treatment protocols holds promise for more personalized care tailored towards patients of diverse subtypes, thereby improving outcomes and mitigating tumor burden, especially for treatment-resistant individuals. In this review, we characterize recent findings surrounding targeted treatments that have been applied to MCC and provide an overview of emerging perspectives on translatable options that can be further developed to offer additional therapeutic avenues for patients with the disease.

Indexed as

Carcinoma, Merkel CellMolecular Targeted TherapySkin NeoplasmsAntineoplastic AgentsHumansProtein Kinase InhibitorsAntineoplastic AgentsProtein Kinase Inhibitorsclinical trialsMerkel cell carcinomareceptor tyrosine kinase inhibitorssomatostatin analogstargeted therapies

Identifiers

PMID39456853
PMCPMC11507330

What OpenQuestion holds

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Registered trials

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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.