Skin Cancer & Melanoma

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At 1 and 2 years, the progression-free survival rates were higher with nivolumab plus ipilimumab vs pembrolizumab in patients with cutaneous melanoma.
Nivolumab/Ipilimumab Improves Real-World Melanoma Outcomes Vs Pembrolizumab

November 12th 2025

At 1 and 2 years, the progression-free survival rates were higher with nivolumab plus ipilimumab vs pembrolizumab in patients with cutaneous melanoma.

One patient with metastatic bladder cancer experienced an ongoing metabolic complete response following treatment with aldesleukin/imneskibart.
Imneskibart Yields Activity and Responses in Melanoma, NSCLC Cohorts

November 11th 2025

Biomarker analyses and real-world comparisons to refine patient selection are ongoing in the phase 2 PLUME trial.
Pembrolizumab Regimen May Show Synergy in Melanoma Populations

November 9th 2025

The 24-month RFS rates were 95.1%, 81.2%, 69.4%, and 48.4% in patients with stage III melanoma who experienced a pCR, near pCR, pPR, pNR, respectively.
Neoadjuvant Nivolumab/Ipilimumab Shows Superior EFS in Resectable Melanoma

November 5th 2025

A Prescription Drug User Fee Act date of April 10, 2026, has been established by the FDA based on a Class II resubmission timeline.
FDA Accepts Resubmission of BLA for RP1/Nivolumab in Advanced Melanoma

October 21st 2025

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Vaccine Therapy for Patients With Melanoma

November 1st 1999

Investigation into the therapeutic use of vaccines in patients with metastatic melanoma is critically important because of the lack of effective conventional modalities. The most extensively studied melanoma vaccines in clinical trials are whole-cell preparations or cell lysates that contain multiple antigens capable of stimulating an immune response. Unfortunately, in the majority of studies, immune responses to these vaccines have not translated into a survival advantage. Advances in tumor cell immunology have led to the identification of candidate tumor cell antigens that can stimulate an immune response; this, in turn, has allowed for refinements in vaccine design. However, the exact tumor antigens that should be targeted with a specific vaccine are unknown. The univalent antigen vaccines, which have greater purity, ease of manufacturing, and reproducibility compared with polyvalent vaccines, may suffer from poorer efficacy due to immunoselection and appearance of antigen-negative clones within the tumor. Novel approaches to vaccine design using gene transfection with cytokines and dendritic cells are all promising. However, the induction of immune responses does not necessarily confer a therapeutic benefit. Therefore, these elegant newer strategies need to be studied in carefully designed clinical trials so that outcomes can be compared objectively with standard therapy. If survival is improved with these vaccine approaches, their ease of administration and lack of toxicity will firmly entrench active specific vaccine immunotherapy as a standard modality in the treatment of the melanoma patient.[ONCOLOGY 13(11):1561-1574, 1999].