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Impact of genomic profiling on the treatment and outcomes of patients with advanced gastrointestinal malignancies

机译:基因组谱分析对晚期胃肠道恶性肿瘤患者的治疗和结局的影响

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Abstract The impact of genomic profiling on the outcomes of patients with advanced gastrointestinal (GI) malignancies remains unknown. The primary objectives of the study were to investigate the clinical benefit of genomic-guided therapy, defined as complete response (CR), partial response (PR), or stable disease (SD) at 3 months, and its impact on progression-free survival (PFS) in patients with advanced GI malignancies. Clinical and genomic data of all consecutive GI tumor samples from April, 2013 to April, 2016 sequenced by FoundationOne were obtained and analyzed. A total of 101 samples from 97 patients were analyzed. Ninety-eight samples from 95 patients could be amplified making this approach feasible in 97% of the samples. After removing duplicates, 95 samples from 95 patients were included in the further analysis. Median time from specimen collection to reporting was 11 days. Genomic alteration-guided treatment recommendations were considered new and clinically relevant in 38% (36/95) of the patients. Rapid decline in functional status was noted in 25% (9/36) of these patients who could therefore not receive genomic-guided therapy. Genomic-guided therapy was utilized in 13 patients (13.7%) and 7 patients (7.4%) experienced clinical benefit (6 PR and 1 SD). Among these seven patients, median PFS was 10 months with some ongoing durable responses. Genomic profiling-guided therapy can lead to clinical benefit in a subset of patients with advanced GI malignancies. Attempting genomic profiling earlier in the course of treatment prior to functional decline may allow more patients to benefit from these therapies.
机译:摘要基因组图谱对晚期胃肠道(GI)恶性肿瘤患者预后的影响尚不清楚。该研究的主要目的是研究基因组指导疗法的临床益处,定义为3个月时的完全缓解(CR),部分缓解(PR)或稳定疾病(SD),及其对无进展生存的影响(PFS)患有晚期胃肠道恶性肿瘤的患者。获得并分析了由FoundationOne测序的2013年4月至2016年4月的所有连续GI肿瘤样品的临床和基因组数据。共分析了来自97位患者的101个样本。可以扩增来自95位患者的98个样本,使这种方法在97%的样本中可行。删除重复样本后,来自95个患者的95个样本被包括在进一步分析中。从标本采集到报告的中位时间为11天。在38%(36/95)的患者中,以基因组改变指导的治疗建议被认为是新的且具有临床意义。在这些无法接受基因组指导治疗的患者中,有25%(9/36)注意到功能状态迅速下降。基因组指导疗法用于13例患者(13.7%)和7例患者(7.4%),具有临床获益(6 PR和1 SD)。在这7例患者中,中位PFS为10个月,并有持续的持续反应。基因组概况分析指导的治疗可以使部分胃肠道恶性肿瘤患者受益。在功能下降之前的治疗过程中尽早进行基因组谱分析可以使更多的患者受益于这些疗法。

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