Validation of the prognostic Heidelberg re-irradiation score in an independent mono-institutional patient cohort

被引:25
作者
Niyazi, Maximilian [1 ]
Flieger, Maya [1 ]
Ganswindt, Ute [1 ]
Combs, Stephanie E. [2 ,3 ]
Belka, Claus [1 ]
机构
[1] Univ Munich, Dept Radiat Oncol, D-81377 Munich, Germany
[2] Heidelberg Univ, Dept Radiat Oncol, D-69120 Heidelberg, Germany
[3] Tech Univ Munich, Klinikum Rechts Isar, Dept Radiat Oncol, D-81675 Munich, Germany
关键词
Bevacizumab; Re-irradiation; Radiotherapy; Glioma; Glioblastoma; Heidelberg score; Prognostic; RECURRENT MALIGNANT GLIOMA; HIGH-GRADE GLIOMA; PREDICT SURVIVAL; PHASE-II; GLIOBLASTOMA; BEVACIZUMAB; IRINOTECAN; RADIOCHEMOTHERAPY; CHEMOTHERAPY; RADIOTHERAPY;
D O I
10.1186/1748-717X-9-128
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Re-irradiation has been shown to be a valid option with proven efficacy for recurrent high-grade glioma patients. Overall, up to now it is unclear which patients might be optimal candidates for a second course of irradiation. A recently reported prognostic score developed by Combs et al. may guide treatment decisions and thus, our mono-institutional cohort served as validation set to test its relevance for clinical practice. Patients and methods: The prognostic score is built upon histology, age (< 50 vs. >= 50 years) and the time between initial radiotherapy and re-irradiation (<= 12 vs. > 12 months). This score was initially introduced to distinguish patients with excellent (0 points), good (1 point), moderate (2 points) and poor (3-4 points) post-recurrence survival (PRS) after re-irradiation. Median prescribed radiation dose during re-treatment of recurrent malignant glioma was 36 Gy in 2 Gy single fractions. A substantial part of the patients was additionally treated with bevacizumab (10 mg/kg intravenously at d1 and d15 during re-irradiation). Results: 88 patients (initially 61 WHO IV, 20 WHO III, 7 WHO II) re-irradiated in a single institution were retrospectively analyzed. Median follow-up was 30 months and median PRS of the entire patient cohort 7 months. Seventy-one patients (80.7%) received bevacizumab. PRS was significantly increased in patients receiving bevacizumab (8 vs. 6 months, p = 0.027, log-rank test). KPS, age, MGMT methylation status, sex, WHO grade and the Heidelberg score showed no statistically significant influence on neither PR-PFS nor PRS. Conclusion: In our cohort which was mainly treated with bevacizumab the usefulness of the Heidelberg score could not be confirmed probably due to treatment heterogeneity; it can be speculated that larger multicentric data collections are needed to derive a more reliable score.
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