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Gershenwald, Jeffrey E.

https://orcid.org/0000-0003-4519-5369

Mayo Clinic

The University of Texas MD Anderson Cancer Center

Citations 2

Chemoprevention agents for melanoma: A path forward into phase 3 clinical trials
Jeter, Joanne, Bowles, Tawnya L. , Curiel‐Lewandrowski, Clara , Filipp, Fabian V. , Geskin, Larisa J. , Brewer, Jerry D., Gershenwald, Jeffrey E. , Chu, Emily Y. , Kirkwood, John M. , Funchain, Pauline , Fisher, David E. , Kendra, Kari , Marghoob, Ashfaq A. , Chen, Suephy C. , Ming, Michael E. , Albertini, Mark R. , Vetto, John T. , Margolin, Kim , Hay, Jennifer L. , Ellis, Darrel L., Kashani–Sabet, Mohammed , Mangold, Aaron R. , Nelson, Kelly C. , Powers, Jennifer G. , Sahni, Debjani, Sekulić, Aleksandar , Sondak, Vernon K. , Wei, Maria L. , Thompson, John A. , Weinstock, Martin A. , Cassidy, Pamela B. , Filipp, Fabian V , Mangold, A R , Funchain, Pauline , Jeter, Joanne , Swetter, Susan M. , ABDEL‐MALEK, ZALFA A. , Arbiser, Jack L. , Box, Neil F. , Pagoto, Sherry , Grossman, Douglas , Markovic, Svetomir N. , Robinson, June K. , Zager, Jonathan S. , Dellavalle, Robert Paul , Leachman, Sancy A.

Cancer | October 5, 2018 | Volume: 125 | Issue: 1 | Pages: 18-44

10.1002/cncr.31719 Get It

Recent progress in the treatment of advanced melanoma has led to unprecedented improvements in overall survival and, as these new melanoma treatments have been developed and deployed in the clinic, much has been learned about the natural history of the disease. Now is the time to apply that knowledge toward the design and clinical evaluation of new chemoprevention agents. Melanoma chemoprevention has the potential to reduce dramatically both the morbidity and the high costs associated with treating patients who have metastatic disease. In this work, scientific and clinical melanoma experts from the national Melanoma Prevention Working Group, composed of National Cancer Trials Network investigators, discuss research aimed at discovering and developing (or repurposing) drugs and natural products for the prevention of melanoma and propose an updated pipeline for translating the most promising agents into the clinic. The mechanism of action, preclinical data, epidemiological evidence, and results from available clinical trials are discussed for each class of compounds. Selected keratinocyte carcinoma chemoprevention studies also are considered, and a rationale for their inclusion is presented. These data are summarized in a table that lists the type and level of evidence available for each class of agents. Also included in the discussion is an assessment of additional research necessary and the likelihood that a given compound may be a suitable candidate for a phase 3 clinical trial within the next 5 years.
American Joint Committee on Cancer acceptance criteria for inclusion of risk models for individualized prognosis in the practice of precision medicine
Kattan, Michael W. , Hess, Kenneth R. , Amin, Mahul B. , Lü, Ying , Moons, Karl G.M., Gershenwald, Jeffrey E. , Gimotty, Phyllis A. , Guinney, Justin , Halabi, Susan , Lazar, Alexander J. , Mahar, Alyson , Weiser, Martin R. , Compton, Carolyn C. , Core, members of the AJCC Precision Medicine, Compton, Carolyn, Patel, Tushar P , Sargent, Daniel J. , Core, members of the AJCC Precision Medicine, Mahar, Alyson L , Lazar, Alexander J , Halabi, Susan , Lu, Ying , Kattan, Michael W

CA: A Cancer Journal for Clinicians | January 19, 2016 | Volume: 66 | Issue: 5 | Pages: 370-374

10.3322/caac.21339 Get It

The American Joint Committee on Cancer (AJCC) has increasingly recognized the need for more personalized probabilistic predictions than those delivered by ordinal staging systems, particularly through the use of accurate risk models or calculators. However, judging the quality and acceptability of a risk model is complex. The AJCC Precision Medicine Core conducted a 2‐day meeting to discuss characteristics necessary for a quality risk model in cancer patients. More specifically, the committee established inclusion and exclusion criteria necessary for a risk model to potentially be endorsed by the AJCC. This committee reviewed and discussed relevant literature before creating a checklist unique to this need of AJCC risk model endorsement. The committee identified 13 inclusion and 3 exclusion criteria for AJCC risk model endorsement in cancer. The emphasis centered on performance metrics, implementation clarity, and clinical relevance. The facilitation of personalized probabilistic predictions for cancer patients holds tremendous promise, and these criteria will hopefully greatly accelerate this process. Moreover, these criteria might be useful for a general audience when trying to judge the potential applicability of a published risk model in any clinical domain. CA Cancer J Clin 2016;66:370–374. © 2016 American Cancer Society.