Muacevic Alexander, Kreth Friedrich W
Department of Neurosurgery, Klinikum Grosshadern, Ludwig-Maximilians-University, Marchioninistr. 15, 81377 Munich, Germany.
J Neurol. 2003 May;250(5):561-8. doi: 10.1007/s00415-003-1036-x.
Prognostic factors are poorly defined for the elderly subpopulation with glioblastoma multiforme and have been exclusively related to conventional survival analysis. In this study an additional quality adjusted survival analysis (QAS) was performed. The prognostic evaluation of both survival- and QAS data after standard treatment were checked for concordant/discordant findings. Their usefulness for estimation of treatment effects and treatment strategies was then evaluated.
123 patients >or= 65 years of age with a supratentorial, de novo glioblastoma were included in the current retrospective report. Microsurgery plus radiation therapy (planned tumor dose: 60 Gy) was performed in 58 patients, and radiation therapy alone after stereotactic biopsy (planned tumor dose: 60 Gy) in 65 patients. The functional status of each patient was scored when joining the study and at every follow-up using 15 selected neurological signs and symptoms (NSSs). Gradation of severity of each NSS was performed with subjective weights. Survival time of each patient was adjusted according to any changes in these NSSs to become the Quality Time (Q-TIME). Time intervals spent with side effects of the treatment (TOX) were subtracted from Q-TIME to become the patient's QAS (QAS = Q-TIME-TOX). Prognostic factors for both survival and QAS were obtained from the Cox model.
Overall survival and QAS were 24 weeks and 10.5 weeks, respectively. Perioperative morbidity and mortality were 5.2 % and 1.7 % in the surgery group and 1.5 % and 1.5 % in the biopsy group, respectively (p > 0.05). Tumor resection gained favorable prognostic importance for patients with midline shift in terms of both survival and QAS (p < 0.0001). Otherwise, radiation therapy alone was as effective as surgery plus radiation therapy (concordant finding). A pretreatment Karnofsky Score (KPS) < 70 was an unfavorable predictor for QAS (p < 0.002) but not for survival (discordant finding). Median QAS for patients with a pretreatment KPS < 70 was only 10 weeks. Age did not reach prognostic relevance.
The dramatic decrease of QAS as compared with survival indicates extremely limited posttreatment improvement and/or rapid deterioration of the neurological score after standard treatment for the older subpopulation with glioblastoma multiforme. Supportive treatment should be considered for patients with a pretreatment KPS < 70.
多形性胶质母细胞瘤老年亚群的预后因素定义尚不明确,且一直仅与传统生存分析相关。本研究进行了额外的质量调整生存分析(QAS)。对标准治疗后生存数据和QAS数据的预后评估进行一致性/不一致性检查。然后评估它们在估计治疗效果和治疗策略方面的有用性。
本回顾性报告纳入了123例年龄≥65岁的幕上原发性胶质母细胞瘤患者。58例患者接受了显微手术加放射治疗(计划肿瘤剂量:60 Gy),65例患者在立体定向活检后仅接受放射治疗(计划肿瘤剂量:60 Gy)。在患者入组研究时以及每次随访时,使用15项选定的神经体征和症状(NSS)对每位患者的功能状态进行评分。对每个NSS的严重程度进行主观加权分级。根据这些NSS的任何变化调整每位患者的生存时间,以得出质量时间(Q-TIME)。从Q-TIME中减去治疗副作用所花费的时间间隔(TOX),得出患者的QAS(QAS = Q-TIME - TOX)。从Cox模型中获得生存和QAS的预后因素。
总生存期和QAS分别为24周和10.5周。手术组围手术期发病率和死亡率分别为5.2%和1.7%,活检组分别为1.5%和1.5%(p>0.05)。就生存和QAS而言,肿瘤切除对中线移位患者具有良好的预后意义(p<0.0001)。否则,单纯放射治疗与手术加放射治疗效果相同(一致性结果)。治疗前卡诺夫斯基评分(KPS)<70是QAS的不良预测因素(p<0.002),但不是生存的不良预测因素(不一致性结果)。治疗前KPS<70的患者的中位QAS仅为10周。年龄未达到预后相关性。
与生存期相比,QAS显著降低表明多形性胶质母细胞瘤老年亚群在标准治疗后治疗后改善极其有限和/或神经评分迅速恶化。对于治疗前KPS<70的患者应考虑给予支持性治疗。