Reirradiation of recurrent high-grade glioma and development of prognostic scores for progression and survival

被引:24
|
作者
Chapman, Christopher H. [1 ]
Hara, Jared H. [2 ]
Molinaro, Annette M. [3 ,4 ]
Clarke, Jennifer L. [3 ,5 ]
Bush, Nancy Ann Oberheim [3 ,5 ]
Taylor, Jennie W. [3 ,5 ]
Butowski, Nicholas A. [3 ]
Chang, Susan M. [3 ]
Fogh, Shannon E. [1 ]
Sneed, Penny K. [1 ]
Nakamura, Jean L. [1 ]
Raleigh, David R. [1 ]
Braunstein, Steve E. [1 ]
机构
[1] Univ Calif San Francisco, Dept Radiat Oncol, 1600 Divisadero St,Ste H1031, San Francisco, CA 94143 USA
[2] Univ Hawaii, John A Burns Sch Med, Honolulu, HI 96822 USA
[3] Univ Calif San Francisco, Dept Neurol Surg, San Francisco, CA 94143 USA
[4] Univ Calif San Francisco, Dept Epidemiol & Biostat, San Francisco, CA 94143 USA
[5] Univ Calif San Francisco, Dept Neurol, San Francisco, CA 94143 USA
关键词
glioblastoma; glioma; prognosis; recurrence; reirradiation; HYPOFRACTIONATED STEREOTACTIC REIRRADIATION; RADIATION-THERAPY; GLIOBLASTOMA; RADIOTHERAPY; RADIOSURGERY; BEVACIZUMAB; EFFICACY; MANAGEMENT; CRITERIA; SYSTEM;
D O I
10.1093/nop/npz017
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background. Optimal techniques and patient selection for salvage reirradiation of high-grade glioma (HGG) are unclear. In this study, we identify prognostic factors for freedom from progression (FFP) and overall survival (OS) after reirradiation, risk factors for high-grade toxicity, and validate clinical prognostic scores. Methods. A total of 116 patients evaluated between 2000 and 2018 received reirradiation for HGG (99 WHO grade IV, 17 WHO grade III). Median time to first progression after initial therapy was 10.6 months. Salvage therapies before reirradiation included surgery (31%) and systemic therapy (41%). Sixty-five patients (56%) received single-fraction stereotactic radiosurgery (SRS) as reirradiation. The median biologically effective dose (BED) was 47.25 Gy, and the median planning target volume (PTV) was 4.8 cc for SRS and 95.0 cc for non-SRS treatments. Systemic therapy was given concurrently to 52% and adjuvantly to 74% of patients. Results. Median FFP was 4.9 months, and median OS was 11.0 months. Significant multivariable prognostic factors for FFP were performance status, time to initial progression, and BED; for OS they were age, time to initial progression, and PTV volume at recurrence. High-grade toxicity was correlated to PTV size at recurrence. Three-level prognostic scores were generated for FFP and OS, with cross-validated receiver operating characteristic area under the curve (AUC) of 0.640 and 0.687, respectively. Conclusions. Clinical variables at the time of reirradiation for HGG can be used to prognosticate FFP and OS.
引用
收藏
页码:364 / 374
页数:11
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