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Precision Medicine Tumor Boards: Clinical Applicability of Personalized Treatment Concepts in Ovarian Cancer

机译:精密医学肿瘤委员会:个性化治疗概念在卵巢癌中的临床适用性

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摘要

Background: Treating cancer according to its molecular alterations (i.e., targeted treatment, TT) is the goal of precision medicine tumor boards (PTBs). Their clinical applicability has been evaluated for ovarian cancer patients in this analysis. Methods: All consecutive ovarian cancer patients discussed in a PTB at the Medical University of Vienna, Austria, from April 2015 to April 2019 were included ( = 44). Results: In 38/44 (86%) cases, at least one mutation, deletion or amplification was detected. The most frequently altered genes were p53 (64%), PI3K pathway (18%), KRAS (14%), BRCA1 (11%) and BRCA2 (2%). In 31 patients (70%) a TT was recommended. A total of 12/31 patients (39%) received the recommended therapy. Median time from indication for PTB to TT start was 65 days (15–216). Median time to treatment failure was 2.7 months (0.2–13.2). Clinical benefit rate (CBR) was 42%. Reasons for treatment discontinuation were disease progression (42%), poor performance status (PS > 2; 25%), death (17%) or treatment related side effects (8%). In 61% the TT was not administered—mainly due to PS > 2. Conclusion: Even though a TT recommendation can be derived frequently, clinical applicability remains limited due to poor patients’ general condition after exploitation of standard treatment. However, we observed antitumor activity in a substantial number of heavily pretreated patients.
机译:背景:根据其分子变化(即靶向治疗,TT)治疗癌症是精密医学肿瘤板(PTB)的目标。在此分析中,已评估了其对卵巢癌患者的临床适用性。方法:纳入2015年4月至2019年4月在奥地利维也纳医科大学的PTB中讨论的所有连续卵巢癌患者(= 44)。结果:在38/44(86%)病例中,至少检测到一种突变,缺失或扩增。改变最频繁的基因是p53(64%),PI3K途径(18%),KRAS(14%),BRCA1(11%)和BRCA2(2%)。建议在31例患者(70%)中使用TT。共有12/31例患者(39%)接受了推荐的治疗。从显示PTB到开始TT的中位时间为65天(15–216)。治疗失败的中位时间为2.7个月(0.2-13.2)。临床受益率(CBR)为42%。中止治疗的原因是疾病进展(42%),表现不佳(PS> 2; 25%),死亡(17%)或治疗相关的副作用(8%)。在61%的患者中未进行TT治疗-主要是因为PS>2。结论:尽管TT推荐可经常获得,但由于采用标准治疗后患者的总体状况较差,因此临床应用仍然受到限制。但是,我们在大量经过严格治疗的患者中观察到了抗肿瘤活性。

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