Nørøxe Dorte Schou, Østrup Olga, Yde Christina Westmose, Ahlborn Lise Barlebo, Nielsen Finn Cilius, Michaelsen Signe Regner, Larsen Vibeke Andrée, Skjøth-Rasmussen Jane, Brennum Jannick, Hamerlik Petra, Poulsen Hans Skovgaard, Lassen Ulrik
Department of Radiation Biology, Rigshospitalet, 2100 Copenhagen, Denmark.
Department of Oncology, Rigshospitalet, 2100 Copenhagen, Denmark.
Oncotarget. 2019 Jul 9;10(43):4397-4406. doi: 10.18632/oncotarget.27030.
Glioblastoma (GB) is an incurable brain cancer with limited treatment options. The aim was to test the feasibility of using cell-free DNA (cfDNA) to support evaluation of treatment response, pseudo-progression and whether progression could be found before clinical and/or radiologic progression. CfDNA fluctuated during treatment with the highest levels before diagnostic surgery and at progression. An increase was seen in 3 out of 4 patients at the time of progression while no increase was seen in 3 out of 4 patients without progression. CfDNA levels could aid in 3 out of 3 questionable cases of pseudo-progression. Eight newly diagnosed GB patients were included. Blood samples were collected prior to diagnosis, before start and during oncologic treatment until progression. Seven patients received concurrent radiotherapy/Temozolomide with adjuvant Temozolomide with one of the patients included in a clinical trial with either immunotherapy or placebo as add-on. One patient received radiation alone. CfDNA concentration was determined for each blood sample. It was feasible to measure cfDNA concentration. Despite the limited cohort size, there was a good tendency between cfDNA and treatment course and -response, respectively with the highest levels at progression.
胶质母细胞瘤(GB)是一种无法治愈的脑癌,治疗选择有限。目的是测试使用游离DNA(cfDNA)来支持评估治疗反应、假性进展以及是否能在临床和/或影像学进展之前发现病情进展的可行性。cfDNA在治疗期间波动,在诊断性手术前和病情进展时水平最高。4例病情进展患者中有3例在病情进展时cfDNA水平升高,而4例无病情进展患者中有3例未见升高。cfDNA水平有助于判断3例可疑的假性进展病例。纳入了8例新诊断的GB患者。在诊断前、开始肿瘤治疗前以及治疗期间直至病情进展时采集血样。7例患者接受同步放疗/替莫唑胺及辅助性替莫唑胺治疗,其中1例患者纳入一项临床试验,该试验将免疫疗法或安慰剂作为附加治疗。1例患者仅接受放疗。测定每个血样的cfDNA浓度。测量cfDNA浓度是可行的。尽管队列规模有限,但cfDNA与治疗过程及反应之间分别存在良好的趋势,病情进展时水平最高。