Chahlavi Ali, Kanner Andrew, Peereboom David, Staugaitis Susan M, Elson Paul, Barnett Gene
Department of Neurological Surgery, Brain Tumor Institute, Cleveland Clinic Cancer Center, Cleveland Clinic, Cleveland, OH 44195, USA.
J Neurooncol. 2003 Feb;61(3):267-73. doi: 10.1023/a:1022580610598.
In this IRB-approved retrospective study, we analyzed the efficacy of temozolomide on World Health Organization Grade II and III oligodendrogliomas, as well as mixed oligoastrocytomas, to determine if a correlation exists between the tumors' 1p status and control of growth by this new oral agent. We assessed six patients with oligodendrogliomas with 1p intact (38%) and 10 patients with 1p loss (62%), who received temozolomide. Chromosome 1p status was significantly associated with response to treatment using temozolomide. While nine of 10 patients (90%) with 1p loss responded to temozolomide, only two of six patients (33%) with 1p intact benefited from this treatment (p = 0.04). Although the number of patients evaluated was small, there was no association between 1p status and gender, age, and tumor grade. Gender, age, and tumor grade were similarly not correlated with response to chemotherapy. This report is the first to find that patients harboring oligodendrogliomas with 1p loss are more likely to be sensitive to treatment with temozolomide than those that retain this chromosomal element. Larger prospective trials are needed to confirm these findings; however, temozolomide should be considered in the management of these tumors.
在这项经机构审查委员会批准的回顾性研究中,我们分析了替莫唑胺对世界卫生组织二级和三级少突胶质细胞瘤以及混合性少突星形细胞瘤的疗效,以确定肿瘤的1p状态与这种新型口服药物对肿瘤生长的控制之间是否存在相关性。我们评估了6例1p完整的少突胶质细胞瘤患者(38%)和10例1p缺失的患者(62%),这些患者均接受了替莫唑胺治疗。1p染色体状态与替莫唑胺治疗反应显著相关。10例1p缺失患者中有9例(90%)对替莫唑胺有反应,而6例1p完整患者中只有2例(33%)从该治疗中获益(p = 0.04)。尽管评估的患者数量较少,但1p状态与性别、年龄和肿瘤分级之间无关联。性别、年龄和肿瘤分级与化疗反应同样无关。本报告首次发现,与保留该染色体元件的患者相比,患有1p缺失少突胶质细胞瘤的患者对替莫唑胺治疗更敏感。需要更大规模的前瞻性试验来证实这些发现;然而,在这些肿瘤的治疗中应考虑使用替莫唑胺。