Powell Steven F, Dib Elie G, Bleeker Jonathan S, Keppen Michael D, Mazurczak Miroslaw, Hack Keely M, Gitau Mark M, Steen Preston D, Terstriep Shelby A, Reynolds John, Landsverk Megan L, Chan Chun-Hung, Nelson Morgan E, Thompson Paul A, Ellison Christie, Black Lora J, Ford James M, Chung Jon H, Anhorn Rachel, Gaba Anu G
Steven F. Powell, Elie G. Dib, Jonathan S. Bleeker, Michael D. Keppen, Miroslaw Mazurczak, Keely M. Hack, Megan L. Landsverk, and Chun-Hung Chan, Sanford Cancer Center; Morgan E. Nelson, Paul A. Thompson, Christie Ellison, and Lora J. Black, Sanford Research, Sioux Falls, SD; Mark M. Gitau, Preston D. Steen, Shelby A. Terstriep, and Anu G. Gaba, Roger Maris Cancer Center, Fargo; John Reynolds, Sanford Cancer Center, Bismarck, ND; James M. Ford, Stanford University School of Medicine, Stanford, CA; Jon H. Chung and Rachel Anhorn, Foundation Medicine, Cambridge, MA.
JCO Precis Oncol. 2018 Nov;2:1-12. doi: 10.1200/PO.17.00220.
Precision oncology (PO) is a growing treatment approach in the era of next-generation sequencing (NGS) and matched therapies. Effective delivery of PO in the community has not been extensively studied. Our program developed a virtual molecular tumor board (MTB) strategy to help guide PO care.
Over 18 months, eligible adult patients with advanced, incurable solid tumor malignancies were enrolled in a molecular profiling (MP) study using the Foundation Medicine NGS panel. Results were reviewed through a weekly, videoconferenced MTB conducted across our largely rural integrated health system. Recommendations from the MTB were used to identify actionable alterations (AAs). Feasibility of PO care delivery was assessed as the primary outcome. Secondary outcomes included the frequency of AAs, genomic matched treatments, genomic matched clinical trial enrollment, and clinical outcomes.
A total of 120 participants with a variety of advanced tumor types were enrolled. Of these, 109 (90.8%) had successful MP. Treatment on the basis of an AA was recommended by the MTB in 58% of patients (63 of 109) who had a successful MP result. For those completing MP, treatments included enrollment in a genomic matched clinical trial (n = 16; 14.6%) and genomic matched treatment with a Food and Drug Administration-approved agent (n = 23; 21.1%). Response and survival data were similar regardless of the matched treatment option chosen.
A video-conferenced MTB-facilitated NGS testing and treatment delivery system was implemented in our integrated community oncology program. Continued use of this model aims to increase understanding of the impact of PO in this setting.
精准肿瘤学(PO)是下一代测序(NGS)和匹配疗法时代不断发展的治疗方法。社区中PO的有效实施尚未得到广泛研究。我们的项目制定了虚拟分子肿瘤委员会(MTB)策略,以帮助指导PO治疗。
在18个月的时间里,符合条件的成年晚期、不可治愈实体瘤恶性肿瘤患者参加了一项使用Foundation Medicine NGS检测板的分子谱分析(MP)研究。通过我们主要为农村地区的综合卫生系统每周进行的视频会议MTB对结果进行审查。MTB的建议用于确定可操作的改变(AA)。将PO治疗实施的可行性作为主要结果进行评估。次要结果包括AA的频率、基因组匹配治疗、基因组匹配临床试验入组情况和临床结果。
共招募了120名患有各种晚期肿瘤类型的参与者。其中,109名(90.8%)成功进行了MP。在成功获得MP结果的患者中,58%(109名中的63名)的MTB建议根据AA进行治疗。对于完成MP的患者,治疗包括参加基因组匹配的临床试验(n = 16;14.6%)和使用美国食品药品监督管理局批准的药物进行基因组匹配治疗(n = 23;21.1%)。无论选择何种匹配治疗方案,反应和生存数据相似。
我们的综合社区肿瘤项目实施了一个通过视频会议MTB促进的NGS检测和治疗交付系统。持续使用该模型旨在增进对PO在这种情况下影响的理解。