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Precision medicine: preliminary results from the Initiative for Molecular Profiling and Advanced Cancer Therapy 2 (IMPACT2) study

机译:精密药:分子分析和晚期癌症治疗的初步结果2(影响2)研究

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Precision medicine is associated with favorable outcomes in selected patients with cancer. Herein, we report an interim analysis of IMPACT2, an ongoing randomized study evaluating genomic profiling and targeted agents in metastatic cancer. Patients with metastatic cancer underwent tumor genomic profiling (ClinialTrials.gov: NCT02152254), and 69 patients met the criteria for randomization. Tumor board and multidisciplinary review of molecular alterations optimized treatment selection. From 5/2014 to 4/2017, 320 patients (median age, 63 years; men, 47%) had tumor molecular aberrations, and 213 (66.56%) received anticancer therapy. The most frequently mutated genes were TP53 (42%), KRAS (16%), PIK3CA (12%), and CDKN2A (11%). The median OS was 10.9 months (95% CI, 8.8–12.9). OS was shorter in patients with higher tumor mutational burden. Independent factors associated with shorter OS were age ≥60 years, liver metastases, low albumin levels, high LDH levels, and KRAS and TP53 mutations. Outcomes for randomized patients will be reported after completion of the study.
机译:精确药物与癌症患者的有利结果有关。在此,我们报告了对影响的临时分析2,一种正在进行的随机研究评估转移性癌症中的基因组分析和靶向剂。转移性癌症的患者接受了肿瘤基因组分析(ClinialTrials.gov:NCT02152254),69名患者达到了随机化的标准。肿瘤委员会和多学科审查分子改变优化治疗选择。从2014年5月2011年至2017年,320名患者(中位年龄,63岁;男性,47%)具有肿瘤分子像畸变,213(66.56%)接受抗癌治疗。最常突变的基因是TP53(42%),KRAS(16%),PIK3CA(12%)和CDKN2A(11%)。中位数OS为10.9个月(95%CI,8.8-12.9)。肿瘤突变负担患者患者较短。与较短OS相关的独立因素≥60岁,肝转移,低白蛋白水平,高LDH水平和KRA和TP53突变。随机患者的结果将在研究完成后报告。

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