Norden Andrew D, Drappatz Jan, Muzikansky Alona, David Karly, Gerard Mary, McNamara M Brenna, Phan Phuong, Ross Ainsley, Kesari Santosh, Wen Patrick Y
Division of Neuro-Oncology, Department of Neurology, Brigham and Women's Hospital, 75 Francis St, Boston, MA 02115, USA.
J Neurooncol. 2009 Apr;92(2):149-55. doi: 10.1007/s11060-008-9745-8. Epub 2008 Nov 29.
Recent clinical trial results suggest that anti-angiogenic therapy may be effective against recurrent malignant glioma. Though these treatments prolong progression-free survival, the extent to which they prolong overall survival is unknown. We pooled data from 34 patients treated at a single institution on phase II clinical trials of bevacizumab and cediranib, and we compared these data to 18 patients treated on clinical trials of cytotoxic chemotherapies. In univariate and multivariate analyses, treatment group was a significant predictor of progression-free but not overall survival. Median progression-free survival was 8 vs. 22 weeks in patients treated with cytotoxic as compared to anti-angiogenic therapy (P = 0.01). Median overall survival was nearly identical in the two groups (39 vs. 37 weeks). The results of this exploratory analysis suggest that anti-angiogenic therapy may fail to prolong overall survival in patients with recurrent malignant glioma. If this conclusion proves correct, progression-free survival may be an inappropriate endpoint for phase II trials of anti-angiogenic therapies.
近期临床试验结果表明,抗血管生成疗法可能对复发性恶性胶质瘤有效。尽管这些治疗可延长无进展生存期,但它们对总生存期的延长程度尚不清楚。我们汇总了在单一机构接受贝伐单抗和西地尼布II期临床试验治疗的34例患者的数据,并将这些数据与接受细胞毒性化疗临床试验治疗的18例患者的数据进行了比较。在单变量和多变量分析中,治疗组是无进展生存期的显著预测因素,但不是总生存期的预测因素。与抗血管生成疗法相比,接受细胞毒性治疗的患者中位无进展生存期为8周,而抗血管生成治疗组为22周(P = 0.01)。两组的中位总生存期几乎相同(39周对37周)。这项探索性分析的结果表明,抗血管生成疗法可能无法延长复发性恶性胶质瘤患者的总生存期。如果这一结论被证明是正确的,那么无进展生存期可能不适用于抗血管生成疗法II期试验的终点。