Chapman Paul B
From the Melanoma Section, Melanoma and Immunotherapeutics Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, Weill Cornell Medical College, New York, NY.
Am Soc Clin Oncol Educ Book. 2014:16-9. doi: 10.14694/EdBook_AM.2014.34.16.
In recent years the expectation related to treating patients with metastatic melanoma has changed. Three years ago, a diagnosis of metastatic melanoma was bleak; only a small number of patients would benefit from standard treatment and the reason for treatment benefit was often unknown, leaving physicians with limited options to help their patients. Today, just 3 years later, there are proven therapies that allow physicians to expect to shrink tumors and extend the lives of their patients after diagnosis. In this article, Paul B. Chapman, MD, Memorial Sloan Kettering Cancer Center, summarizes the recent advances in the field of metastatic melanoma and looks ahead to topics such as focusing on specificity, shutting down the ERK pathway, intermittent dosing, discovering driver mutations, individualizing checkpoint inhibition, and identifying rejection antigens to identify what should occur next in order to continue to improve outcomes for a larger population of patients with metastatic melanoma. Dr. Chapman's paper reminds us of the exciting progress that has been made while focusing on the work that is left in the field. Dr. Chapman is a physician-scientist who specializes in diagnosing and treating melanoma that has metastasized to other parts of the body. Dr. Chapman led a clinical trial that paved the way, in part, to the approval of vemurafenib-a drug that targets a BRAF mutation that is present in approximately 50% of patients with metastatic melanoma. Dr. Chapman is one of five Memorial Sloan Kettering scientists to be appointed to a melanoma "Dream Team" that focuses on identifying potential therapies for metastatic melanoma patients who do not have the mutated form of the BRAF gene. Dr. Chapman is also a professor of medicine at the Weill Cornell Medical College and is the chair of the Melanoma Research Alliance Medical Advisory Board. In addition to the above, Dr. Chapman is a sought-after mentor for medical oncology fellows and has a current research interest in identifying novel means to more durably block signaling in the MAPK pathway in melanoma cells. Jedd Wolchok, MD, PhD, Scientific Program Committee Chair.
近年来,对于转移性黑色素瘤患者的治疗期望已经发生了变化。三年前,转移性黑色素瘤的诊断前景黯淡;只有少数患者能从标准治疗中获益,而且治疗获益的原因往往不明,这使得医生帮助患者的选择有限。然而,仅仅3年后的今天,已有经过验证的疗法,使医生在诊断后有望缩小肿瘤并延长患者生命。在本文中,纪念斯隆凯特琳癌症中心的医学博士保罗·B·查普曼总结了转移性黑色素瘤领域的最新进展,并展望了诸如关注特异性、阻断ERK通路、间歇给药、发现驱动突变、个性化检查点抑制以及识别排斥抗原等主题,以确定为了继续改善更多转移性黑色素瘤患者的治疗效果接下来应该做些什么。查普曼博士的论文在关注该领域剩余工作的同时,也让我们想起了已经取得的令人振奋的进展。查普曼博士是一位临床医生兼科学家,专门从事诊断和治疗已转移至身体其他部位的黑色素瘤。查普曼博士领导了一项临床试验,该试验部分为维莫非尼的获批铺平了道路,维莫非尼是一种靶向约50%转移性黑色素瘤患者中存在的BRAF突变的药物。查普曼博士是被任命加入黑色素瘤“梦之队”的五位纪念斯隆凯特琳科学家之一,该团队专注于为没有BRAF基因变异形式的转移性黑色素瘤患者确定潜在疗法。查普曼博士还是威尔康奈尔医学院的医学教授,并且是黑色素瘤研究联盟医学顾问委员会主席。除此之外,查普曼博士是备受追捧的肿瘤医学研究员导师,目前的研究兴趣在于确定更持久地阻断黑色素瘤细胞中MAPK通路信号传导的新方法。杰德·沃尔乔克,医学博士、哲学博士,科学项目委员会主席