Department of Neurological Surgery, Wakayama Medical University School of Medicine, Kimiidera 811-1, Wakayama, 641-0012, Japan.
Kansai Molecular Diagnosis Network for CNS Tumors, Osaka, Japan.
J Neurooncol. 2018 Nov;140(2):329-339. doi: 10.1007/s11060-018-2957-7. Epub 2018 Aug 3.
This study investigates the current state of clinical practice and molecular analysis for elderly patients with diffuse gliomas and aims to elucidate treatment outcomes and prognostic factors of patients with glioblastomas.
We collected elderly cases (≥ 70 years) diagnosed with primary diffuse gliomas and enrolled in Kansai Molecular Diagnosis Network for CNS Tumors. Clinical and pathological characteristics were analyzed retrospectively. Various factors were evaluated in univariate and multivariate models to examine their effects on overall survival.
Included in the study were 140 elderly patients (WHO grade II: 7, III: 19, IV: 114), median age was 75 years. Sixty-seven patients (47.9%) had preoperative Karnofsky Performance Status score of ≥ 80. All patients underwent resection (gross-total: 20.0%, subtotal: 14.3%, partial: 39.3%, biopsy: 26.4%). Ninety-six of the patients (68.6%) received adjuvant treatment consisting of radiotherapy (RT) with temozolomide (TMZ). Seventy-eight of the patients (75.0%) received radiation dose of ≥ 50 Gy. MGMT promoter was methylated in 68 tumors (48.6%), IDH1/2 was wild-type in 129 tumors (92.1%), and TERT promoter was mutated in 78 of 128 tumors (60.9%). Median progression-free and overall survival of grade IV cases was 8.2 and 13.6 months, respectively. Higher age (≥ 80 years) and TERT promoter mutated were associated with shorter survival. Resection and adjuvant RT + TMZ were identified as independent factors for good prognosis.
This community-based study reveals characteristics and outcomes of elderly glioma patients in a real-world setting. Elderly patients have several potential factors for poor prognosis, but resection followed by RT + TMZ could lengthen duration of survival.
本研究旨在探讨老年弥漫性神经胶质瘤患者的临床实践和分子分析现状,并阐明胶质母细胞瘤患者的治疗结果和预后因素。
我们收集了在关西中枢神经系统肿瘤分子诊断网络中诊断为原发性弥漫性神经胶质瘤的老年病例(≥70 岁)。回顾性分析临床和病理特征。在单变量和多变量模型中评估了各种因素,以检查它们对总生存期的影响。
研究纳入了 140 名老年患者(WHO 分级 II:7 例,III:19 例,IV:114 例),中位年龄为 75 岁。67 例患者(47.9%)术前 Karnofsky 表现状态评分≥80。所有患者均行切除术(全切除:20.0%,次全切除:14.3%,部分切除:39.3%,活检:26.4%)。96 例患者(68.6%)接受了辅助治疗,包括替莫唑胺联合放疗(RT)。78 例患者(75.0%)接受了≥50 Gy 的放疗剂量。68 例肿瘤中 MGMT 启动子甲基化(48.6%),129 例肿瘤中 IDH1/2 野生型(92.1%),128 例肿瘤中有 78 例 TERT 启动子突变(60.9%)。IV 级病例的中位无进展生存期和总生存期分别为 8.2 个月和 13.6 个月。较高的年龄(≥80 岁)和 TERT 启动子突变与较短的生存期相关。切除和辅助 RT+TMZ 被确定为良好预后的独立因素。
本基于社区的研究揭示了老年神经胶质瘤患者在真实环境中的特征和结局。老年患者存在多种预后不良的潜在因素,但切除后行 RT+TMZ 可延长生存期。