Kesari Santosh, Schiff David, Henson John W, Muzikansky Alona, Gigas Debra C, Doherty Lisa, Batchelor Tracy T, Longtine Janina A, Ligon Keith L, Weaver Susan, Laforme Andrea, Ramakrishna Naren, Black Peter McL, Drappatz Jan, Ciampa Abigail, Folkman Judah, Kieran Mark, Wen Patrick Y
Dana-Farber/Brigham and Women's Cancer Center, Center for Neuro-Oncology, 44 Binney St., SW430D, Boston, MA 02115, USA.
Neuro Oncol. 2008 Jun;10(3):300-8. doi: 10.1215/15228517-2008-005. Epub 2008 Apr 10.
We conducted a phase II study of the combination of temozolomide and angiogenesis inhibitors for treating adult patients with newly diagnosed glioblastoma. Patients who had stable disease following standard radiation therapy received temozolomide for 5 days in 28-day cycles, in combination with daily thalidomide and celecoxib. Patients were treated until tumor progression or development of unacceptable toxicity. Four-month progression-free survival (PFS) from study enrollment was the primary end point, and overall survival (OS) was the secondary end point. In addition, we sought to correlate response with O(6)-methylguanine-DNA methyltransferase promoter methylation status and serum levels of angiogenic peptides. Fifty patients with glioblastoma were enrolled (18 women, 32 men). Median age was 54 years (range, 29-78) and median KPS score was 90 (range, 70-100). From study enrollment, median PFS was 5.9 months (95% confidence interval [CI]: 4.2-8.0) and 4-month PFS was 63% (95% CI: 46%-75%). Median OS was 12.6 months (95% CI: 8.5-16.4) and 1-year OS was 47%. Of the 47 patients evaluable for best response, none had a complete response, five (11%) had partial response, four (9%) had minor response, 22 (47%) had stable disease, and 16 (34%) had progressive disease. Analysis of serial serum samples obtained from 47 patients for four angiogenic peptides failed to show a significant correlation with response or survival for three of the peptides; higher vascular endothelial growth factor levels showed a trend toward correlation with decreased OS (p=0.07) and PFS (p=0.09). The addition of celecoxib and thalidomide to adjuvant temozolomide was well tolerated but did not meet the primary end point of improvement of 4-month PFS from study enrollment.
我们开展了一项II期研究,评估替莫唑胺与血管生成抑制剂联合用药治疗新诊断的成人间变性星形细胞瘤的疗效。接受标准放疗后病情稳定的患者,接受替莫唑胺治疗,每28天为一个周期,连续5天给药,并联合每日服用沙利度胺和塞来昔布。持续治疗直至肿瘤进展或出现不可接受的毒性反应。从入组研究开始计算的4个月无进展生存期(PFS)为主要终点,总生存期(OS)为次要终点。此外,我们试图将疗效与O(6)-甲基鸟嘌呤-DNA甲基转移酶启动子甲基化状态以及血管生成肽的血清水平进行关联分析。共入组50例间变性星形细胞瘤患者(18例女性,32例男性)。中位年龄为54岁(范围29 - 78岁),中位KPS评分为90分(范围70 - 100分)。从入组研究开始计算,中位PFS为5.9个月(95%置信区间[CI]:4.2 - 8.0),4个月PFS率为63%(95% CI:46% - 75%)。中位OS为12.6个月(95% CI:8.5 - 16.4),1年OS率为47%。在可评估最佳疗效的47例患者中,无患者达到完全缓解,5例(11%)部分缓解,4例(9%)轻微缓解,22例(47%)病情稳定,16例(34%)病情进展。对47例患者的系列血清样本进行4种血管生成肽分析,结果显示其中3种肽与疗效或生存期无显著相关性;血管内皮生长因子水平较高与OS降低(p = 0.07)和PFS降低(p = 0.09)存在一定相关性趋势。在辅助性替莫唑胺治疗中加用塞来昔布和沙利度胺耐受性良好,但未达到从入组研究开始4个月PFS改善的主要终点。