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Pretreatment Tumor DNA Sequencing of KIT and PDGFRA in Endosonography-Guided Biopsies Optimizes the Preoperative Management of Gastrointestinal Stromal Tumors

机译:预处理肿瘤DNA测序套件和PDGFRA在内皮引导活检中优化了胃肠道间质瘤的术前管理

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Background Neoadjuvant tyrosine kinase inhibitor (TKI) therapy increases the chance of organ-preserving, radical resection in selected patients with gastrointestinal stromal tumors (GISTs). We aimed to evaluate systematic, immediate DNA sequencing of KIT and PDGFRA in pretreatment GIST tissue to guide neoadjuvant TKI therapy and optimize preoperative tumor response. Methods All patients who were candidates for neoadjuvant therapy of a suspected GIST [the study cohort (SC)] were prospectively included from January 2014 to March 2018. Patients were subjected to pretreatment endosonography-guided fine-needle biopsy (EUS-FNB) or transabdominal ultrasound-guided needle biopsy (TUS-NB), followed by immediate tumor DNA sequencing (< 2 weeks). A historic (2006-2013) reference cohort (RC) underwent work-up without sequencing before neoadjuvant imatinib (n = 42). The rate of optimal neoadjuvant therapy (Therapy(OPTIMAL)) was calculated, and the induced tumor size reduction (Tumor Regression(MAX), %) was evaluated by computed tomography (CT) scan. Results The success rate of pretreatment tumor DNA sequencing in the SC (n = 81) was 77/81 (95%) [EUS-FNB 71/74 (96%); TUS-NB 6/7 (86%)], with mutations localized in KIT (n = 58), PDGFRA (n = 18), or neither gene, wild type (n = 5). In patients with a final indication for neoadjuvant therapy, the Therapy(OPTIMAL) was higher in the SC compared with the RC [61/63 (97%) versus 33/42 (79%), p = 0.006], leading to a significantly higher Tumor Regression(MAX) in patients treated with TKI (27% vs. 19%, p = 0.015). Conclusions Pretreatment endosonography-guided biopsy sampling followed by immediate tumor DNA sequencing of KIT and PDGFRA is highly accurate and valuable in guiding neoadjuvant TKI therapy in GIST. This approach minimizes maltreatment with inappropriate regimens and leads to improved tumor size reduction before surgery.
机译:背景技术Neoadjuvant Tyrosine激酶抑制剂(TKI)治疗增加了器官保留的机会,在胃肠道基质肿瘤(GISTS)中的选定患者中的机构。我们旨在评估试剂盒和PDGFRA的系统,即时DNA测序在预处理的GIST组织中,以引导Neoadjuvant TKI治疗并优化术前肿瘤反应。方法对疑似理论的新辅助治疗候选人的所有患者均在2014年1月至2018年3月期间探讨了疑似;研究队长(SC)]。患者进行预处理封面引导的细针活检(EUS-FNB)或TAYABOMINAL引导针活检(TUS-NB),其次是立即肿瘤DNA测序(<2周)。历史悠久的(2006-2013)参考队列(RC)正在进行的工作,而不在Neoadjuvant imatinib之前进行排序(n = 42)。计算出最佳Neoadjuvant治疗率(治疗(最佳)),通过计算机断层扫描(CT)扫描评估诱导的肿瘤大小减少(肿瘤回归(最大),%)。结果SC(n = 81)中预处理肿瘤DNA测序的成功率为77/81(95%)[EUS-FNB 71/74(96%); TUS-NB 6/7(86%)],突变局部化在试剂盒(n = 58),PDGFRA(n = 18),或既不是基因,野生型(n = 5)。在患有Neoadjuvant治疗的最终指示的患者中,与RC相比,SC的治疗(最佳)更高[61/63(97%),与33/42(79%),p = 0.006],导致显着用TKI治疗的患者的患者更高的肿瘤回归(MAX)(27%对19%,P = 0.015)。结论预处理内皮引导的活检采样随后是试剂盒和PDGFRA的直接肿瘤DNA测序,高度准确,有价值的是在GIST中引导新辅助TKI治疗。这种方法使虐待药物减少不适当的方案,并导致手术前改善肿瘤大小减少。

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