This Viewpoint discusses use of anti–PD-1 monotherapy as the primary treatment option for patients with treatment-naive metastatic melanoma staining positive for PD-L1 over dual checkpoint inhibition therapy.
Risultati per: Valutazione e gestione del Melanoma
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Final Results for Adjuvant Dabrafenib plus Trametinib in Stage III Melanoma
New England Journal of Medicine, Ahead of Print.
Gestione antibiotica in caso di infezione del piede diabetico
Neoadjuvant Nivolumab and Ipilimumab in Resectable Stage III Melanoma
New England Journal of Medicine, Ahead of Print.
Keratosis Pilaris–Like Reaction Associated With Chromatin Remodeling Complex Inhibition in Uveal Melanoma
This case series describes a constellation of novel adverse reactions in 3 of 9 patients with uveal melanoma receiving treatment targeting activity of the Brahma-associated factor chromatin remodeling complex.
1261 REGULATION OF INTRAEPITHELIAL CD8+ T CELL INTERACTION WITH EPITHELIAL MHC-I BY ABSENT IN MELANOMA 2 IN GASTRIC PRENEOPLASTIC LESIONS.
Mo1346 COLITIS DIAGNOSIS IN MELANOMA PATIENTS TREATED WITH IMMUNE CHECKPOINT INHIBITORS (ICI) IN REAL-WORLD SETTINGS: TIMING OF ONSET AND PATTERNS OF CARE
Neoadjuvant Dual Checkpoint Inhibitors vs Anti-PD1 Therapy in High-Risk Resectable Melanoma
This pooled analysis of 6 clinical trials describes the safety and efficacy of different courses of immune checkpoint inhibitor treatment in a neoadjuvant setting among patients with high-risk resectable melanoma.
Experience and Fear of Cancer Recurrence Among Survivors of Localized Melanoma
This qualitative and survey-based study uses interviews and surveys to understand the psychological well-being of survivors of localized cutaneous melanoma.
NICE: linee guida sulla diagnosi e gestione dell’endometriosi
Linee guida di consenso per la gestione delle metastasi peritoneali
Adjuvant Immunotherapy in Stage II Melanoma
This Viewpoint reviews the evidence for immune checkpoint inhibitor use in the adjuvant setting, discusses the individual and societal risks, benefits, and costs associated with immune checkpoint inhibitors, and highlights the need for more targeted patient selection approaches.
Considerations in Meta-Analysis of Immunotherapy for Advanced Cancers Other Than Melanoma
To the Editor Serritella and Shenoy conducted an interesting meta-analysis to assess the relative efficacy of nivolumab plus ipilimumab vs nivolumab for the treatment of advanced cancers other than melanoma. Based on 8 studies with 1727 patients (854 in the nivolumab plus ipilimumab group vs 873 in the nivolumab group), the authors concluded that patients in the combination therapy group did not show clinically meaningful overall survival or progression-free survival benefits compared to those in the monotherapy group. Furthermore, treatment-related higher-grade toxicity and discontinuation rates were substantially higher with the combination therapy. However, several methodological issues need to be clarified.
Immunohistochemistry for Diagnosing Melanoma in Older Adults
This retrospective cross-sectional study illustrates national-level trends in immunohistochemistry staining for the diagnosis of melanoma in older adult patients enrolled in Medicare.
Considerations in Meta-Analysis of Immunotherapy for Advanced Cancers Other Than Melanoma—Reply
In Reply I thank Pang and Sun for their comments on our meta-analysis. First, a statement on the key findings: with CheckMate 714 included (see Comment published along with article), the pooled overall survival (OS) and progression-free survival (PFS) hazard ratios (HRs) for nivolumab plus ipilimumab vs nivolumab alone were 0.98 (95% CI, 0.88-1.08) and 0.91 (95% CI, 0.83-1.00), respectively, with 5 of 9 studies having a numerically lower median OS. The combination was associated with substantially higher treatment-related discontinuations and high-grade adverse events. These numbers very strongly support the stated conclusions.
Incidence and Factors in Second Primary Invasive Melanoma in Norway
This cohort study assesses the incidence rate of second primary invasive melanoma at least 30 days after the first based on data from deidentified records of all invasive melanomas diagnosed in 2008 to 2020, obtained from the Cancer Registry of Norway.