Lote K, Egeland T, Hager B, Stenwig B, Skullerud K, Berg-Johnsen J, Storm-Mathisen I, Hirschberg H
Department of Oncology, Norwegian Radium Hospital, Oslo, Norway.
J Clin Oncol. 1997 Sep;15(9):3129-40. doi: 10.1200/JCO.1997.15.9.3129.
We report survival, prognostic factors, and treatment efficacy in low-grade glioma.
A total of 379 patients with histologic intracranial low-grade glioma received post-operative radiotherapy (n = 361) and intraarterial carmustine (BCNU) chemotherapy (n = 153). Overall survival and prognostic factors were evaluated with the SPSS statistical program (SPSS Inc, Chicago, IL).
Median survival (all patients) was 100 months (95% confidence interval [CI], B7 to 113); in age group 0 to 19 years (n = 41), 226 months; in age group 20 to 49 years (n = 263), 106 months; in age group 50 to 59 years (n = 49), 76 months; and for older patients (n = 26), 39 months. Projected survival at 10 and 15 years was 42% and 29%, respectively. Patient age, World Health Organization (WHO) performance status, tumor computed tomography (CT) contrast enhancement, mental changes, or initial corticosteroid dependency were significant independent prognostic factors (p < .05), while histologic subgroup, focal deficits, presence of seizures, prediagnostic symptom duration, tumor category, and tumor stage were not. Patients aged 20 to 49 years with no independent negative prognostic factors (n = 132) had a median survival time of 139 months versus 41 months in patients with two or more factors (n = 33). Patients who presented with symptoms of expansion (n = 97) survived longer when resected (P < .03); otherwise no survival benefit was associated with initial tumor resection compared with biopsy. Intraarterial chemotherapy and radiation doses more than 55 Gy were not associated with prolonged survival. Among 66 reoperated patients, 45% progressed to high-grade histology within 25 months.
Prognosis in low-grade glioma following postoperative radiotherapy seems largely determined by the inherent biology of the glioma and patient age at diagnosis.
我们报告低级别胶质瘤的生存率、预后因素及治疗效果。
共有379例组织学确诊的颅内低级别胶质瘤患者接受了术后放疗(n = 361)及动脉内卡莫司汀(BCNU)化疗(n = 153)。使用SPSS统计软件(SPSS公司,伊利诺伊州芝加哥)评估总生存率及预后因素。
中位生存期(所有患者)为100个月(95%置信区间[CI],87至113);0至19岁年龄组(n = 41)为226个月;20至49岁年龄组(n = 263)为106个月;50至59岁年龄组(n = 49)为76个月;老年患者(n = 26)为39个月。预计10年和15年生存率分别为42%和29%。患者年龄、世界卫生组织(WHO)功能状态、肿瘤计算机断层扫描(CT)增强、精神变化或初始皮质类固醇依赖是显著的独立预后因素(p <.05),而组织学亚组、局灶性缺损、癫痫发作、诊断前症状持续时间、肿瘤类别和肿瘤分期则不是。无独立阴性预后因素的20至49岁患者(n = 132)中位生存时间为139个月,而有两个或更多因素的患者(n = 33)为41个月。出现肿瘤扩大症状的患者(n = 97)手术切除后生存期更长(P <.03);否则,与活检相比,初始肿瘤切除未带来生存获益。动脉内化疗及放疗剂量超过55 Gy与生存期延长无关。在66例再次手术的患者中,45%在25个月内进展为高级别组织学类型。
术后放疗后低级别胶质瘤的预后似乎很大程度上由胶质瘤的内在生物学特性及诊断时的患者年龄决定。