Literature DB >> 32444980

Randomized prospective trial of fractionated stereotactic radiosurgery with chemotherapy versus chemotherapy alone for bevacizumab-resistant high-grade glioma.

David Bergman1, Ankit Modh1, Lonni Schultz2,3, James Snyder2,4, Tom Mikkelsen2,4, Mira Shah1, Samuel Ryu5, M Salim Siddiqui1, Tobias Walbert6,7.   

Abstract

PURPOSE: Outcomes for patients with recurrent high-grade glioma (HGG) progressing on bevacizumab (BEV) are dismal. Fractionated stereotactic radiosurgery (FSRS) has been shown to be feasible and safe when delivered in this setting, but prospective evidence is lacking. This single-institution randomized trial compared FSRS plus BEV-based chemotherapy versus BEV-based chemotherapy alone for BEV-resistant recurrent malignant glioma.
MATERIALS AND METHODS: HGG patients on BEV with tumor progression after 2 previous treatments were randomized to 1) FSRS plus BEV-based chemotherapy or 2) BEV-based chemotherapy with irinotecan, etoposide, temozolomide, or carboplatin. FSRS was delivered as 32 Gy (8 Gy × 4 fractions within 2 weeks) to the gross target volume and 24 Gy (6 Gy × 4 fractions) to the clinical target volume (fluid-attenuated inversion recovery abnormality). The primary endpoints were local control (LC) at 2 months and progression-free survival (PFS).
RESULTS: Of the 35 patients enrolled, 29 had glioblastoma (WHO IV) and 6 had anaplastic glioma (WHO III). The median number of prior recurrences was 3. Patients treated with FSRS had significantly improved PFS (5.1 vs 1.8 months, P < .001) and improved LC at 2 months (82% [14/17] vs 27% [4/15], P = .002). The overall median survival was 6.6 months (7.2 months with FSRS vs 4.8 months with chemotherapy alone, P = .11).
CONCLUSIONS: FSRS combined with BEV-based chemotherapy in recurrent HGG patients progressing on BEV is feasible and improves LC and PFS when compared to treatment with BEV-based chemotherapy alone.

Entities:  

Keywords:  Bevacizumab; Fractionated radiosurgery; Glioblastoma; High-grade glioma; Re-irradiation

Mesh:

Substances:

Year:  2020        PMID: 32444980     DOI: 10.1007/s11060-020-03526-4

Source DB:  PubMed          Journal:  J Neurooncol        ISSN: 0167-594X            Impact factor:   4.130


  5 in total

1.  Clinical outcomes of dose-escalated re-irradiation in patients with recurrent high-grade glioma.

Authors:  Corbin A Helis; Shih-Ni Prim; Christina K Cramer; Roy Strowd; Glenn J Lesser; Jaclyn J White; Stephen B Tatter; Adrian W Laxton; Christopher Whitlow; Hui-Wen Lo; Waldemar Debinski; James D Ververs; Paul J Black; Michael D Chan
Journal:  Neurooncol Pract       Date:  2022-05-02

2.  High-dose salvage re-irradiation for recurrent/progressive adult diffuse glioma: healing or hurting?

Authors:  T Gupta; M Maitre; P Maitre; J S Goda; R Krishnatry; A Chatterjee; A Moiyadi; P Shetty; S Epari; A Sahay; V Patil; R Jalali
Journal:  Clin Transl Oncol       Date:  2021-02-02       Impact factor: 3.405

3.  Genomic alterations predictive of response to radiosurgery in recurrent IDH-WT glioblastoma.

Authors:  Antonio Dono; Mark Amsbaugh; Magda Martir; Richard H Smilie; Roy F Riascos; Jay-Jiguang Zhu; Sigmund Hsu; Dong H Kim; Nitin Tandon; Leomar Y Ballester; Angel I Blanco; Yoshua Esquenazi
Journal:  J Neurooncol       Date:  2021-01-25       Impact factor: 4.130

4.  Heterogeneity of radiation response in mesenchymal subtype glioblastoma: molecular profiling and reactive oxygen species generation.

Authors:  Christopher P Cifarelli; Angelica Jacques; Andrey Bobko
Journal:  J Neurooncol       Date:  2021-02-10       Impact factor: 4.130

5.  Salvage therapies for radiation-relapsed isocitrate dehydrogenase-mutant astrocytoma and 1p/19q codeleted oligodendroglioma.

Authors:  Sirui Ma; Soumon Rudra; Jian L Campian; Milan G Chheda; Tanner M Johanns; George Ansstas; Christopher D Abraham; Michael R Chicoine; Eric C Leuthardt; Joshua L Dowling; Gavin P Dunn; Albert H Kim; Jiayi Huang
Journal:  Neurooncol Adv       Date:  2021-06-18
  5 in total

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