Department of Neurology, University Medical Center Regensburg, Universitätsstrasse 84, 93053, Regensburg, Germany.
J Neurooncol. 2011 Sep;104(3):801-9. doi: 10.1007/s11060-011-0548-y. Epub 2011 Mar 4.
The objective of this prospective, monocentric phase-II pilot study was to evaluate toxicity and efficacy of neoadjuvant temozolomide (TMZ) and 13-cis retinoic acid (13-cRA) treatment in patients with newly diagnosed anaplastic gliomas after total or subtotal tumor resection. The primary endpoint of the study was median progression-free survival (PFS). Secondary endpoints were toxicity and PFS rates at 6, 12 and 24 months. Thirty-two adult patients were included in the study and treated with a median number of 10 TMZ and 13-cRA cycles (range 1-26). The majority of patients had favorable prognostic factors characterized by young age, complete resection, oligodendroglial histology, 1p/19q co-deletion, O6-methylguanine-DNA methyltransferase (MGMT) promotor methylation and isocitrate dehydrogenase 1 (IDH1) mutation. Grade 3/4 myelotoxicity occurred in 5/32 patients, and about 90% of patients suffered from grade 2/3 adverse events attributable to 13-cRA. The median PFS was 37.8 months (95% CI 22.2-53.4). The 6-, 12- and 24-month PFS rates were 84.4, 75 and 42.4%. The extent of tumor resection was the only prognostic factor associated with better PFS. TMZ and 13-cRA treatment did not improve PFS when retrospectively compared to the TMZ-treated group within the randomized NOA-04 phase-III trial. In conclusion, 13-cRA addition to TMZ in a neoadjuvant setting showed acceptable toxicity, but did not yield an advantage in PFS in patients with newly diagnosed anaplastic gliomas after total or subtotal tumor resection.
本前瞻性、单中心 II 期试点研究的目的是评估新诊断的高级别胶质瘤患者在全切除或近全切除肿瘤后接受替莫唑胺(TMZ)和 13-顺式维甲酸(13-cRA)新辅助治疗的毒性和疗效。该研究的主要终点是无进展生存期(PFS)的中位数。次要终点是治疗 6、12 和 24 个月时的毒性和 PFS 率。该研究纳入了 32 名成年患者,中位接受 TMZ 和 13-cRA 治疗周期数为 10 个(范围为 1-26 个)。大多数患者具有良好的预后因素,包括年龄较小、完全切除、少突胶质细胞瘤组织学、1p/19q 共缺失、O6-甲基鸟嘌呤-DNA 甲基转移酶(MGMT)启动子甲基化和异柠檬酸脱氢酶 1(IDH1)突变。5/32 名患者发生 3/4 级骨髓毒性,约 90%的患者发生归因于 13-cRA 的 2/3 级不良事件。中位 PFS 为 37.8 个月(95%CI 22.2-53.4)。6、12 和 24 个月的 PFS 率分别为 84.4%、75%和 42.4%。肿瘤切除范围是唯一与更好的 PFS 相关的预后因素。与随机 III 期 NOA-04 试验中的 TMZ 治疗组相比,TMZ 和 13-cRA 治疗在回顾性比较时并未改善 PFS。总之,在新诊断的高级别胶质瘤患者中,替莫唑胺联合 13-cRA 在新辅助治疗中的毒性可接受,但在全切除或近全切除肿瘤后并未改善 PFS。