ReviewPharmacological research2025
Advances in Cutaneous Melanoma Therapy: The Emerging Role of CDK4/6 Inhibitors.
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.
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.
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.
Who cites it
3 citing papers in PubMed.
- The Role of Transcriptional and Atypical Cyclin-Dependent Protein Kinases in Melanoma.Cancers · 2026Review
- Review
- Advancing precision immuno-oncology in melanoma: the synergistic convergence of personalized neoantigen vaccines and multi-omics biomarker profiling.Frontiers in immunology · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
6 authors.
Funding
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.
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Identifiers
What OpenQuestion holds
Registered trials
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.