Hildebrand Jerzy, Gorlia Thierry, Kros Johan M, Afra Dénes, Frenay Marc, Omuro Antonio, Stupp Roger, Lacombe Denis, Allgeier Anouk, van den Bent Martin J
Hopital Universitaire Erasme, Brussels, Belgium.
Eur J Cancer. 2008 Jun;44(9):1210-6. doi: 10.1016/j.ejca.2007.12.005. Epub 2008 Jan 14.
In a previous randomised EORTC study on adjuvant dibromodulcitol (DBD) and bichloroethylnitrosourea (BCNU) in adults with glioblastoma multiforme (GBM) and anaplastic astrocytoma (AA), a clinically significant trend towards a longer overall survival (OS) and a progression-free survival (PFS) was observed in the subgroup of AA. The aim of the present study was to test this adjuvant regimen in a larger number of AA patients.
Continuation of the previous phase III trial for newly diagnosed AA according to the local pathologist. Patients were randomised to either radiotherapy only or to radiotherapy in combination with BCNU on day 2 and weekly DBD, followed by adjuvant DBD and BCNU in cycles of six weeks for a maximum total treatment duration of one year. OS was the primary end-point.
Patients (193 ) with newly diagnosed AA according to local pathological assessment were randomised to radiotherapy (RT) alone (n=99), or to RT plus DBD/BCNU (n=94); 12 patients were considered not eligible. At central pathology review, over half (53%) of the locally diagnosed AA cases could not be confirmed. On intent-to-treat analysis, no statistically significant differences in OS (p=0.111) and PFS (p=0.087) were observed, median OS after RT was only 23.9 months 95% confidence interval (CI), [18.4-34.0] after RT plus DBD/BCNU 27.3 months 95% CI [21.4-46.8].
No statistically significant improvement in survival was observed after BCNU/DBD adjuvant chemotherapy in AA patients. The trend towards improved survival is consistent with previous reports. Central pathology review of grade 3 tumours remains crucial.
在先前一项欧洲癌症研究与治疗组织(EORTC)针对多形性胶质母细胞瘤(GBM)和间变性星形细胞瘤(AA)成人患者的辅助性二溴卫矛醇(DBD)和双氯乙基亚硝脲(BCNU)的随机研究中,在AA亚组中观察到总体生存期(OS)和无进展生存期(PFS)有临床显著延长的趋势。本研究的目的是在更多AA患者中测试这种辅助治疗方案。
根据当地病理学家的诊断,继续对新诊断的AA患者进行先前的III期试验。患者被随机分为仅接受放疗组或放疗联合第2天的BCNU及每周一次的DBD组,随后进行为期六周的辅助性DBD和BCNU治疗,最长总治疗时长为一年。OS是主要终点。
根据当地病理评估,193例新诊断的AA患者被随机分为单纯放疗组(n = 99)或放疗加DBD/BCNU组(n = 94);12例患者被认为不符合条件。在中心病理复查时,超过一半(53%)的当地诊断为AA的病例无法得到确认。在意向性分析中,未观察到OS(p = 0.111)和PFS(p = 0.087)有统计学显著差异,放疗后的中位OS仅为23.9个月,95%置信区间(CI)为[18.4 - 34.0],放疗加DBD/BCNU后的中位OS为27.3个月,95%CI为[21.4 - 46.8]。
在AA患者中,BCNU/DBD辅助化疗后未观察到生存期有统计学显著改善。生存期改善的趋势与先前报告一致。对3级肿瘤进行中心病理复查仍然至关重要。