Continuous Low-Dose Temozolomide Chemotherapy and Microvessel Density in Recurrent Glioblastoma
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 : Thi...
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Veröffentlicht in: | Journal of Korean Neurosurgical Society 2015, Vol.58 (5), p.426-431 |
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description | 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 $50mg/m^2/day$ 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 $22.7{\pm}24.1/mm^2$ (mean${\pm}$standard deviation), and this was lower than that of the initial tumor ($61.4{\pm}32.7/mm^2$) (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. |
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Methods : Thirty patients who had recurrent GBM following Stupp's regimen received TMZ daily at $50mg/m^2/day$ 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 $22.7{\pm}24.1/mm^2$ (mean${\pm}$standard deviation), and this was lower than that of the initial tumor ($61.4{\pm}32.7/mm^2$) (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.</description><identifier>ISSN: 2005-3711</identifier><identifier>EISSN: 1598-7876</identifier><language>kor</language><ispartof>Journal of Korean Neurosurgical Society, 2015, Vol.58 (5), p.426-431</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,4024</link.rule.ids></links><search><creatorcontrib>Woo, Jong-Yun</creatorcontrib><creatorcontrib>Yang, Seung Ho</creatorcontrib><creatorcontrib>Lee, Youn Soo</creatorcontrib><creatorcontrib>Lee, Su Youn</creatorcontrib><creatorcontrib>Kim, Jeana</creatorcontrib><creatorcontrib>Hong, Yong Kil</creatorcontrib><title>Continuous Low-Dose Temozolomide Chemotherapy and Microvessel Density in Recurrent Glioblastoma</title><title>Journal of Korean Neurosurgical Society</title><addtitle>대한신경외과학회지</addtitle><description>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 $50mg/m^2/day$ 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 $22.7{\pm}24.1/mm^2$ (mean${\pm}$standard deviation), and this was lower than that of the initial tumor ($61.4{\pm}32.7/mm^2$) (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.</description><issn>2005-3711</issn><issn>1598-7876</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>JDI</sourceid><recordid>eNqNys9qwkAQgPGlVGiovsNcPAZ2VzeJR4nV0j8I4j2sZsTBzU7JbBT79O2hD9DTxw--B5UZt6jysiqLR5VZrV0-K415UhMROmhdOW2NKzLV1BwTxYEHgQ--5SsWhD12_M2BO2oR6vOv0hl7_3UHH1v4pGPPVxTBACuMQukOFGGHx6HvMSbYBOJD8JK482M1OvkgOPnrs5quX_b1a34hSdTEVkLztnzfWm2cNtYVppy7ws7--_0Ak_lFfQ</recordid><startdate>2015</startdate><enddate>2015</enddate><creator>Woo, Jong-Yun</creator><creator>Yang, Seung Ho</creator><creator>Lee, Youn Soo</creator><creator>Lee, Su Youn</creator><creator>Kim, Jeana</creator><creator>Hong, Yong Kil</creator><scope>JDI</scope></search><sort><creationdate>2015</creationdate><title>Continuous Low-Dose Temozolomide Chemotherapy and Microvessel Density in Recurrent Glioblastoma</title><author>Woo, Jong-Yun ; Yang, Seung Ho ; Lee, Youn Soo ; Lee, Su Youn ; Kim, Jeana ; Hong, Yong Kil</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-kisti_ndsl_JAKO2015012561745623</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>kor</language><creationdate>2015</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Woo, Jong-Yun</creatorcontrib><creatorcontrib>Yang, Seung Ho</creatorcontrib><creatorcontrib>Lee, Youn Soo</creatorcontrib><creatorcontrib>Lee, Su Youn</creatorcontrib><creatorcontrib>Kim, Jeana</creatorcontrib><creatorcontrib>Hong, Yong Kil</creatorcontrib><collection>KoreaScience</collection><jtitle>Journal of Korean Neurosurgical Society</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Woo, Jong-Yun</au><au>Yang, Seung Ho</au><au>Lee, Youn Soo</au><au>Lee, Su Youn</au><au>Kim, Jeana</au><au>Hong, Yong Kil</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Continuous Low-Dose Temozolomide Chemotherapy and Microvessel Density in Recurrent Glioblastoma</atitle><jtitle>Journal of Korean Neurosurgical Society</jtitle><addtitle>대한신경외과학회지</addtitle><date>2015</date><risdate>2015</risdate><volume>58</volume><issue>5</issue><spage>426</spage><epage>431</epage><pages>426-431</pages><issn>2005-3711</issn><eissn>1598-7876</eissn><abstract>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 $50mg/m^2/day$ 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 $22.7{\pm}24.1/mm^2$ (mean${\pm}$standard deviation), and this was lower than that of the initial tumor ($61.4{\pm}32.7/mm^2$) (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.</abstract><oa>free_for_read</oa></addata></record> |
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title | Continuous Low-Dose Temozolomide Chemotherapy and Microvessel Density in Recurrent Glioblastoma |
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