Literature DB >> 28561661

Operable Melanoma: Screening, Prognostication, and Adjuvant and Neoadjuvant Therapy.

Ahmad A Tarhini1, Paul Lorigan1, Sancy Leachman1.   

Abstract

The importance of reducing the numbers of patients with late-stage melanoma, identifying which patients are most likely to progress, and treating these patients at the earliest possible stage cannot be overemphasized. Improved screening of patients prior to diagnosis has the advantage of identifying early-stage disease that is for the most part treatable by surgical methods. The process of melanoma screening is rapidly evolving through population-based programs, mobile health technologies, and advanced imaging tools. For patients with newly diagnosed melanoma, accurately estimating disease prognosis has important implications for management and follow-up. Prognostic factors are individual host- or tumor-related factors or molecules that correlate with genetic predisposition and clinical course. These include clinical covariates and host and tumor proteomic/genomic markers that allow the prognostic subclassification of patients. Adjuvant therapy for high-risk surgically resected melanoma targets residual micrometastatic disease with the goal of reducing the risk of relapse and mortality. In the United States, three regimens have achieved regulatory approval for adjuvant therapy, including high-dose interferon alpha, pegylated interferon alpha, and ipilimumab at 10 mg/kg. Phase III trials have reported benefits in relapse-free survival (all regimens) and overall survival (high-dose interferon alpha and ipilimumab). The management of locally/regionally advanced melanoma may benefit from neoadjuvant therapy, which is the subject of several ongoing studies. Recent studies have shown promising clinical activity and yielded important biomarker findings and mechanistic insights.

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Year:  2017        PMID: 28561661     DOI: 10.1200/EDBK_174930

Source DB:  PubMed          Journal:  Am Soc Clin Oncol Educ Book        ISSN: 1548-8748


  4 in total

1.  A unique gene expression signature is significantly differentially expressed in tumor-positive or tumor-negative sentinel lymph nodes in patients with melanoma.

Authors:  Ahmad A Tarhini; Theofanis Floros; Hui-Min Lin; Yan Lin; Zahra Rahman; Madeeha Ashraf; Priyanka Vallabhaneni; Cindy Sander; Uma N M Rao; Monica Panelli; William A LaFramboise; John M Kirkwood
Journal:  Melanoma Res       Date:  2017-10       Impact factor: 3.599

2.  Functional assessment of cancer therapy questionnaire for melanoma in the Serbian population: A factor analytic approach.

Authors:  Suzana Matkovic; Jelena Dotlic; Tatjana Gazibara; Gorica Maric; Vladimir Nikolic; Natasa Maksimovic
Journal:  PLoS One       Date:  2021-06-30       Impact factor: 3.240

3.  An Economic Evaluation of Pembrolizumab Versus Other Adjuvant Treatment Strategies for Resected High-Risk Stage III Melanoma in the USA.

Authors:  Arielle G Bensimon; Zheng-Yi Zhou; Madeline Jenkins; Yan Song; Wei Gao; James Signorovitch; Clemens Krepler; Emilie Scherrer; Jingshu Wang; Raquel Aguiar-Ibáñez
Journal:  Clin Drug Investig       Date:  2020-07       Impact factor: 2.859

4.  Neoadjuvant ipilimumab (3 mg/kg or 10 mg/kg) and high dose IFN-α2b in locally/regionally advanced melanoma: safety, efficacy and impact on T-cell repertoire.

Authors:  Ahmad Tarhini; Yan Lin; Huang Lin; Zahra Rahman; Priyanka Vallabhaneni; Prateek Mendiratta; James F Pingpank; Matthew P Holtzman; Erik C Yusko; Julie A Rytlewski; Uma N M Rao; Robert L Ferris; John M Kirkwood
Journal:  J Immunother Cancer       Date:  2018-10-23       Impact factor: 13.751

  4 in total

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