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논문 기본 정보

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학술저널
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Gwak, Ho-Shin (Registration Group) Yee, Gi Taek (Registration Group) Park, Chul-Kee (Registration Group) Kim, Jin Wook (Registration Group) Hong, Yong-Kil (Registration Group) Kang, Seok-Gu (Registration Group) Kim, Jeong Hoon (Registration Group) Seol, Ho Jun (Registration Group) Jung, Tae-Young (Registration Group) Chang, Jong Hee (Registration Group) Yoo, Heon (Registration Group) Hwang, Jeong-Hyun (Registration Group) Kim, Se-Hyuk (Registration Group) Park, Bong Jin (Registration Group) Hwang, Sun-Chul (Registration Group) Kim, Min Su (Registration Group) Kim, Seon-Hwan (Registration Group) Kim, Eun-Young (Registration Group) Kim, Ealmaan (Registration Group) Kim, Hae Yu (Registration Group) Ko, Young-Cho (Registration Group) Yun, Hwan Jung (Registration Group) Youn, Ji Hye (Registration Group) Kim, Juyoung (Korean Society for Neuro-Oncology, Pharmaceutical Benefit Department, Health Insurance Review and Assessment Service) Lee, Byeongil (Korean Society for Neuro-Oncology, Pharmaceutical Benefit Department, Health Insurance Review and Assessment Service) Lee, Seung Hoon (Registration Group)
저널정보
대한신경외과학회 대한신경외과학회지 대한신경외과학회지 제54권 제6호
발행연도
2013.1
수록면
489 - 495 (7page)

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Objective : To evaluate the efficacy of temozolomide (TMZ) chemotherapy for recurrent anaplastic oligodendroglioma (AO) and anaplastic oligoastrocytoma (AOA). Methods : A multi-center retrospective trial enrolled seventy-two patients with histologically proven AO/AOA who underwent TMZ chemotherapy for their recurrent tumors from 2006 to 2010. TMZ was administered orally (150 to 200 $mg/m^2/day$) for 5 days per 28 days until unacceptable toxicity occurred or tumor progression was observed. Results : TMZ chemotherapy cycles administered was median 5.3 (range, 1-41). The objective response rate was 24% including 8 cases (11%) of complete response and another 23 patients (32%) were remained as stable disease. Severe side effects (${\geq}$grade 3) occurred only in 9 patients (13%). Progression-free survival (PFS) of all patients was a median 8.0 months (95% confidence interval, 6.0-10.0). The time to recurrence of a year or after was a favorable prognostic factor for PFS (p<0.05). Overall survival (OS) was apparently differed by the patient's histology, as AOA patients survived a median OS of 18.0 months while AO patients did not reach median OS at median follow-up of 11.5 months (range 2.7-65 months). Good performance status of Eastern Cooperative Oncology Group 0 and 1 showed prolonged OS (p<0.01). Conclusion : For recurrent AO/AOA after surgery followed by radiation therapy, TMZ could be recommended as a salvage therapy at the estimated efficacy equal to procarbazine, lomustine, and vincristine (PCV) chemotherapy at first relapse. For patients previously treated with PCV, TMZ is a favorable therapeutic option as 2nd line salvage chemotherapy with an acceptable toxicity rate.

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