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Concurrent Chemoradiotherapy with Temozolomide Followed by Adjuvant Temozolomide for Newly Diagnosed Glioblastoma Patients: A Retrospective Multicenter Observation Study in Korea.

Authors :
Kim BS
Seol HJ
Nam DH
Park CK
Kim IH
Kim TM
Kim JH
Cho YH
Yoon SM
Chang JH
Kang SG
Kim EH
Suh CO
Jung TY
Lee KH
Kim CY
Kim IA
Hong CK
Yoo H
Kim JH
Kang SH
Kang MK
Kim EY
Kim SH
Chung DS
Hwang SC
Song JH
Cho SJ
Lee SI
Lee YS
Ahn KJ
Kim SH
Lim DH
Gwak HS
Lee SH
Hong YK
Source :
Cancer research and treatment [Cancer Res Treat] 2017 Jan; Vol. 49 (1), pp. 193-203. Date of Electronic Publication: 2016 Jun 27.
Publication Year :
2017

Abstract

Purpose: The purpose of this study was to investigate the feasibility and survival benefits of combined treatment with radiotherapy and adjuvant temozolomide (TMZ) in a Korean sample.<br />Materials and Methods: A total of 750 Korean patients with histologically confirmed glioblastoma multiforme, who received concurrent chemoradiotherapy with TMZ (CCRT) and adjuvant TMZ from January 2006 until June 2011, were analyzed retrospectively.<br />Results: After the first operation, a gross total resection (GTR), subtotal resection (STR), partial resection (PR), biopsy alone were achieved in 388 (51.7%), 159 (21.2%), 96 (12.8%), and 107 (14.3%) patients, respectively. The methylation status of O <superscript>6</superscript> -methylguanine-DNA methyltransferase (MGMT) was reviewed retrospectively in 217 patients. The median follow-up period was 16.3 months and the median overall survival (OS) was 17.5 months. The actuarial survival rates at the 1-, 3-, and 5-year OS were 72.1%, 21.0%, and 9.0%, respectively. The median progression-free survival (PFS) was 10.1 months, and the actuarial PFS at 1-, 3-, and 5-year PFS were 42.2%, 13.0%, and 7.8%, respectively. The patients who received GTR showed a significantly longer OS and PFS than those who received STR, PR, or biopsy alone, regardless of the methylation status of the MGMT promoter. Patients with a methylated MGMT promoter also showed a significantly longer OS and PFS than those with an unmethylated MGMT promoter. Patients who received more than six cycles of adjuvant TMZ had a longer OS and PFS than those who received six or fewer cycles. Hematologic toxicity of grade 3 or 4 was observed in 8.4% of patients during the CCRT period and in 10.2% during the adjuvant TMZ period.<br />Conclusion: Patients treated with CCRT followed by adjuvant TMZ had more favorable survival rates and tolerable toxicity than those who did not undergo this treatment.<br />Competing Interests: relevant to this article was not reported.

Details

Language :
English
ISSN :
2005-9256
Volume :
49
Issue :
1
Database :
MEDLINE
Journal :
Cancer research and treatment
Publication Type :
Academic Journal
Accession number :
27384161
Full Text :
https://doi.org/10.4143/crt.2015.473