Evidence map›Paper›PMID 40967492›Full record

ReviewPharmacological research2025

Advances in Cutaneous Melanoma Therapy: The Emerging Role of CDK4/6 Inhibitors.

Uriel Kim, Thomas S McCormick, Ankit Mangla, Kevin D Cooper, Gary K Schwartz, Akihiro Yoshida

Abstract readReview
In one paragraph

Review in Pharmacological research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Review
  3. 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

6 authors.

Uriel KimCase Comprehensive Cancer Center, Cleveland, OH 44106, USA; Department of Dermatology, Emory University, Atlanta, GA 30322, USA.
Thomas S McCormickDepartment of Dermatology, Case Western Reserve University and University Hospitals Cleveland Medical Center, Cleveland, OH 44106, USA.
Ankit ManglaCase Comprehensive Cancer Center, Cleveland, OH 44106, USA; Department of Hematology and Oncology, Case Western Reserve University and University Hospitals Cleveland Medical Center, Cleveland, OH 44106, USA; University Hospitals Seidman Cancer Center, Cleveland, OH 44106, USA.
Kevin D CooperDepartment of Dermatology, Case Western Reserve University and University Hospitals Cleveland Medical Center, Cleveland, OH 44106, USA.
Gary K SchwartzCase Comprehensive Cancer Center, Cleveland, OH 44106, USA.
Akihiro YoshidaCase Comprehensive Cancer Center, Cleveland, OH 44106, USA; Department of Dermatology, Case Western Reserve University and University Hospitals Cleveland Medical Center, Cleveland, OH 44106, USA. Electronic address: axy234@case.edu.

Funding

Project 5: Microenvironment manipulation using anti-angiogenics to improve immunotherapy in melanomaP50CA254865 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI WANG, HONG · 2021 to 2025
$10.4M
NCI NIH HHS P50 CA254865
6 · The paper itself

Abstract

Cutaneous melanoma is a highly aggressive malignancy; however, recent advancements in targeted and immunologic therapies have significantly improved patient outcomes. MAPK-directed therapies and immune checkpoint inhibitors such as anti-PD-1 and CTLA-4 have increased overall survival for patients with advanced melanoma. Unfortunately, resistance to MAPK-directed therapies and a lack of response to immunotherapy in a subset of patients remain major challenges, underscoring the need for novel therapeutic strategies. The CDK4/6 pathway, which regulates cell cycle progression through the p16-cyclin D-CDK4/6-RB axis, is frequently dysregulated in melanoma, presenting a viable target for therapeutic intervention. CDK4/6 inhibitors (CDK4/6i), which have already demonstrated efficacy in hormone receptor-positive and human epidermal growth factor receptor 2-negative breast cancer, show promise in melanoma by inducing tumor senescence, modulating the tumor microenvironment, and enhancing patient immune responses. Preclinical and translational studies suggest that CDK4/6i could be particularly effective when combined with existing therapies, including MAPK inhibitors, immune checkpoint inhibitors, and senolytic agents. Ongoing clinical trials and emerging data on combination strategies underscore the promise of CDK4/6i as a critical component of future melanoma therapy. This review summarizes the current melanoma treatment landscape and explores the potential of CDK4/6i in advancing melanoma treatment, highlighting their ability to overcome therapy resistance, improve therapeutic efficacy, and offer new strategies for patients with advanced cutaneous melanoma.

Indexed as

Antineoplastic AgentsCyclin-Dependent Kinase 4Cyclin-Dependent Kinase 6MelanomaProtein Kinase InhibitorsSkin NeoplasmsAnimalsHumansAntineoplastic AgentsCDK4 protein, humanCDK6 protein, humanCyclin-Dependent Kinase 4Cyclin-Dependent Kinase 6Protein Kinase InhibitorsCDK4/6 inhibitorsCombination therapyCutaneous melanomaTherapy resistance

Identifiers

PMID40967492
PMCPMC12776930

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.