Harada Shuko, Arend Rebecca, Dai Qian, Levesque Jessica A, Winokur Thomas S, Guo Rongjun, Heslin Martin J, Nabell Lisle, Nabors L Burt, Limdi Nita A, Roth Kevin A, Partridge Edward E, Siegal Gene P, Yang Eddy S
Department of Pathology, University of Alabama at Birmingham, Birmingham, AL, USA.
Department of The Comprehensive Cancer Center, University of Alabama at Birmingham, Birmingham, AL, USA.
Oncotarget. 2017 Jun 14;8(34):57845-57854. doi: 10.18632/oncotarget.18471. eCollection 2017 Aug 22.
With rapid advances in genomic medicine, the complexity of delivering precision medicine to oncology patients across a university health system demanded the creation of a Molecular Tumor Board (MTB) for patient selection and assessment of treatment options. The objective of this report is to analyze our progress to date and discuss the importance of the MTB in the implementation of personalized medicine.
Patients were reviewed in the MTB for appropriateness for comprehensive next generation sequencing (NGS) cancer gene set testing based on set criteria that were in place. Because profiling of stage IV lung cancer, colon cancer, and melanoma cancers were standard of care, these cancer types were excluded from this process. We subsequently analyzed the types of cases referred for testing and approved with regards to their results.
191 cases were discussed at the MTB and 132 cases were approved for testing. Forty-six cases (34.8%) had driver mutations that were associated with an active targeted therapeutic agent, including , and . An additional 56 cases (42.4%) had driver mutations previously reported in some type of cancer. Twenty-two cases (16.7%) did not have any clinically significant mutations. Eight cases did not yield adequate DNA. 15 cases were considered for targeted therapy, 13 of which received targeted therapy. One patient experienced a near complete response. Seven of 13 had stable disease or a partial response.
MTB at University of Alabama-Birmingham is unique because it reviews the appropriateness of NGS testing for patients with recurrent cancer and serves as a forum to educate our physicians about the pathways of precision medicine. Our results suggest that our detection of actionable mutations may be higher due to our careful selection. The application of precision medicine and molecular genetic testing for cancer patients remains a continuous educational process for physicians.
随着基因组医学的迅速发展,在大学健康系统中为肿瘤患者提供精准医疗的复杂性要求设立一个分子肿瘤委员会(MTB),用于患者选择和治疗方案评估。本报告的目的是分析我们迄今为止的进展,并讨论MTB在个性化医疗实施中的重要性。
根据既定标准,在MTB中对患者进行审查,以确定其是否适合进行全面的下一代测序(NGS)癌症基因集检测。由于IV期肺癌、结肠癌和黑色素瘤的基因检测已成为标准治疗手段,因此这些癌症类型被排除在本过程之外。我们随后分析了送检并获批检测的病例类型及其检测结果。
MTB讨论了191例病例,其中132例获批检测。46例(34.8%)有与活性靶向治疗药物相关的驱动突变,包括 、 和 。另外56例(42.4%)有先前在某种癌症中报道过的驱动突变。22例(16.7%)没有任何具有临床意义的突变。8例未获得足够的DNA。15例被考虑进行靶向治疗,其中13例接受了靶向治疗。1例患者出现近乎完全缓解。13例中有7例病情稳定或部分缓解。
阿拉巴马大学伯明翰分校的MTB独具特色,因为它审查了复发性癌症患者进行NGS检测的适宜性,并作为一个论坛,让我们的医生了解精准医疗的途径。我们的结果表明,由于我们的仔细筛选,我们对可操作突变的检测率可能更高。对癌症患者应用精准医疗和分子基因检测对医生来说仍然是一个持续的教育过程。