The prognostic improvement of add-on bevacizumab for progressive disease during concomitant temozolomide and radiation therapy in patients with glioblastoma and anaplastic astrocytoma

被引:6
作者
Yamaguchi, Shigeru [1 ]
Ishi, Yukitomo [1 ]
Motegi, Hiroaki [1 ]
Okamoto, Michinari [1 ]
Kobayashi, Hiroyuki [1 ]
Hirata, Kenji [2 ]
Oda, Yoshitaka [3 ]
Tanaka, Shinya [3 ]
Terasaka, Shunsuke [1 ]
Houkin, Kiyohiro [1 ]
机构
[1] Hokkaido Univ, Fac Med, Dept Neurosurg, North 15 West 7, Sapporo, Hokkaido 0608638, Japan
[2] Hokkaido Univ, Fac Med, Dept Nucl Med, Sapporo, Hokkaido, Japan
[3] Hokkaido Univ, Fac Med, Dept Canc Pathol, Sapporo, Hokkaido, Japan
关键词
Astrocytoma; Bevacizumab; Glioblastoma; Radiotherapy; Temozolomide; PHASE-II; RADIOTHERAPY; IRINOTECAN; GLIOMA; METHYLATION; NEOADJUVANT; EXPRESSION; ADJUVANT; BENEFIT; TRIAL;
D O I
10.23736/S0390-5616.18.04463-6
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
BACKGROUND: Although newly diagnosed high-grade glioma patients in Japan can receive bevacizumab (BEV) as first-line chemotherapy. randomized clinical trials have not shown a survival benefit for BEV for these patients. In this study, we investigated whether selective add-on BEV for patients with newly diagnosed glioblastoma (GBM) and anaplastic astrocytoma (AA) improves prognosis, in cases where tumors were continuously growing during radiotherapy concomitant with temozolomide (TMZ). METHODS: We conducted a retrospective survey of the overall survival (OS) of patients with GBM;AAs who were treated in our institution between 2006 and 2016. Patients whose tumors were continuously growing regardless of radiotherapy were categorized as the "progressive" group; remaining patients were categorized as the "non-progressive" group. Since 2013, patients in the "progressive" group received add-on BEV therapy with the Stupp regimen during or just after radiotherapy. RESULTS: Of 151 GBM/AA patients, 34 (22.5%) were categorized in the "progressive" group. Median OSs of the "progressive" and "nonprogressive" groups were 13.2 months and 25.3 months, respectively (P<0.001). Twelve patients in the "progressive" group received add-on BEV therapy, and their median OS was 20.2 months; whereas for the remaining 22 patients in the "progressive" group who were treated before the BEV era, their median OS was 10.5 months. In the "progressive" group, add-on BEV significantly extended OS (P 0.018) and was the lone clinical factor of better prognosis. CONCLUSIONS: We found that, for patients with GBM/AAs whose tumors were continuously growing during radiotherapy, add-on BEV treatment resulted in survival benefits.
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页码:502 / 508
页数:7
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