Wong E T, Hess K R, Gleason M J, Jaeckle K A, Kyritsis A P, Prados M D, Levin V A, Yung W K
Departments of Neuro-Oncology and Biomathematics, The University of Texas M.D. Anderson Cancer Center, Houston, TX 77030, USA.
J Clin Oncol. 1999 Aug;17(8):2572-8. doi: 10.1200/JCO.1999.17.8.2572.
To determine aggregate outcomes and prognostic covariates in patients with recurrent glioma enrolled onto phase II chemotherapy trials.
Patients from eight consecutive phase II trials included 225 with recurrent glioblastoma multiforme (GBM) and 150 with recurrent anaplastic astrocytoma (AA). Their median age was 45 years (range, 15 to 82 years) and their median Karnofsky performance score was 80 (range, 60 to 100). Prognostic covariates were analyzed with respect to tumor response, progression-free survival (PFS), and overall survival (OS) by multivariate logistic and Cox proportional hazards regression analyses.
Overall, 34 (9%) had complete or partial response, whereas 80 (21%) were alive and progression-free at 6 months (APF6). The median PFS was 10 weeks and median OS was 30 weeks. Histology was a robust prognostic factor across all outcomes. GBM patients had significantly poorer outcomes than AA patients. The APF6 proportion was 15% for GBM and 31% for AA, whereas the median PFS was 9 weeks for GBM and 13 weeks for AA. Results were also significantly poorer for patients with more than two prior surgeries or chemotherapy regimens.
Histology is a dominant factor in determining outcome in patients with recurrent glioma enrolled onto phase II trials. Future trials should be designed with separate histology strata.
确定纳入II期化疗试验的复发性胶质瘤患者的总体疗效及预后协变量。
来自8项连续II期试验的患者包括225例复发性多形性胶质母细胞瘤(GBM)患者和150例复发性间变性星形细胞瘤(AA)患者。他们的中位年龄为45岁(范围15至82岁),中位卡氏评分(Karnofsky performance score)为80分(范围60至100分)。通过多变量逻辑回归和Cox比例风险回归分析,对预后协变量在肿瘤反应、无进展生存期(PFS)和总生存期(OS)方面进行分析。
总体而言,34例(9%)有完全或部分缓解,而80例(21%)在6个月时存活且无进展(APF6)。中位PFS为10周,中位OS为30周。组织学是所有疗效指标中强有力的预后因素。GBM患者的疗效明显比AA患者差。GBM患者的APF6比例为15%,AA患者为31%,而GBM患者的中位PFS为9周,AA患者为13周。对于接受过两次以上既往手术或化疗方案的患者,结果也明显较差。
组织学是决定纳入II期试验的复发性胶质瘤患者预后的主要因素。未来试验应按不同组织学分层设计。