Continuous Low-Dose Temozolomide Chemotherapy and Microvessel Density in Recurrent Glioblastoma

被引:15
|
作者
Woo, Jong-Yun [1 ]
Yang, Seung Ho [3 ]
Lee, Youn Soo [2 ]
Lee, Su Youn [1 ]
Kim, Jeana [4 ]
Hong, Yong Kil [1 ]
机构
[1] Catholic Univ Korea, Seoul St Marys Hosp, Dept Neurosurg, 222 Banpo Daero, Seoul 06591, South Korea
[2] Catholic Univ Korea, Seoul St Marys Hosp, Dept Pathol, Seoul 06591, South Korea
[3] Catholic Univ Korea, St Vincents Hosp, Dept Neurosurg, Suwon, South Korea
[4] Catholic Univ Korea, Bucheon St Marys Hosp, Dept Hosp Pathol, Bucheon, South Korea
关键词
Glioblastoma; Temozolomide; Metronomic chemotherapy; Microvessel density; PHASE-II TRIAL; HIGH-GRADE GLIOMA; MALIGNANT GLIOMA; INTENSE TEMOZOLOMIDE; METRONOMIC CHEMOTHERAPY; FACTOR EXPRESSION; BRAIN-TUMORS; LUNG-CANCER; RADIOTHERAPY; SURVIVAL;
D O I
10.3340/jkns.2015.58.5.426
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective : The purpose of this study was to evaluate the clinical efficacy of continuous low-dose temozolomide (TMZ) chemotherapy for recurrent and TMZ-refractory glioblastoma multiforme (GBM) and to study the relationship between its efficacy and microvessel density within the tumor. Methods : Thirty patients who had recurrent GBM following Stupp's regimen received TMZ daily at 50 mg/m(2)/day until tumor progression between 2007 and 2013. The median duration of continuous low-dose TMZ administration was 8 weeks (range, 2-64). Results : The median progression-free survival (PFS) of continuous low-dose TMZ therapy was 2 months (range, 0.5-16). At 6 months, PFS was 20%. The median overall survival (OS) from the start of this therapy to death was 6 months (95% CI : 5.1-6.9). Microvessel density of recurrent tumor tissues obtained by reoperation of 17 patients was 22.7 +/- 24.1/mm(2) (mean +/- standard deviation), and this was lower than that of the initial tumor (61.4 +/- 32.7/mm(2)) (p-value=0.001). It suggests that standard TMZ-chemoradiotherapy reduces the microvessel density within GBM and that recurrences develop in tumor cells with low metabolic burden. The efficacy of continuous low-dose TMZ could not be expected in recurrent GBM cells in poor angiogenic environments. Conclusion : The efficacy of continuous low-dose TMZ chemotherapy is marginal. This study suggests the need to develop further treatment strategies for recurrent and TMZ-refractory GBM.
引用
收藏
页码:426 / 431
页数:6
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