Improvement, clinical course, and quality of life after palliative radiotherapy for recurrent glioblastoma
- PMID: 18525311
- DOI: 10.1097/COC.0b013e31815e3fdc
Improvement, clinical course, and quality of life after palliative radiotherapy for recurrent glioblastoma
Abstract
The purpose of this review is to assess the palliative effect of re-irradiation in adult patients with recurrent supratentorial glioblastoma (GBM) previously treated with adjuvant or primary radiation therapy, with or without chemotherapy. From a comprehensive literature search, studies were identified reporting on survival, progression, and quality of life endpoints including, but not limited to, EORTC QLQ-C30 questionnaire, clinical symptoms, and ability to reduce dexamethasone. Data from more than 300 GBM patients (grade 3 anaplastic gliomas were excluded) demonstrate that re-irradiation yields 6-month PFS of 28% to 39% and 1-year overall survival of 18% to 48%, without additional chemotherapy (median value 26%). Patients with Karnofsky performance status <70 appeared to be at higher risk of early progression and apparently had lesser benefit from re-irradiation. Clinical improvement was observed in 24% to 45% of the patients. Most studies suggest that stabilization of the performance status is a realistic aim. In the studies reporting on corticosteroid usage during and after re-irradiation, 20% to 60% of the patients achieved a reduction in steroid dependency. Serious late toxicity was uncommon, especially after conventional treatment and fractionated stereotactic radiotherapy (FSRT). In light of recent technological advances such as FSRT and intensity modulated radiotherapy, which permit maximal sparing of normal brain, re-treatment seems attractive, and deserves scientific validation. Even fraction sizes of 3 to 5 Gy seem to be well tolerated in limited-volume recurrences as long as the total dose is limited to 30 to 35 Gy. Salvage chemotherapy or targeted agents should be prospectively tested against re-irradiation alone.
Similar articles
-
Radiotherapy in supratentorial gliomas. A study of 821 cases.Strahlenther Onkol. 2003 Sep;179(9):606-14. doi: 10.1007/s00066-003-1098-9. Strahlenther Onkol. 2003. PMID: 14628126
-
[Role of radiotherapy in recurrent gliomas].Bull Cancer. 2004 Nov;91(11):883-9. Bull Cancer. 2004. PMID: 15582893 Review. French.
-
Phase I/II trial of hyperfractionated concomitant boost proton radiotherapy for supratentorial glioblastoma multiforme.Int J Radiat Oncol Biol Phys. 2010 May 1;77(1):98-105. doi: 10.1016/j.ijrobp.2009.04.054. Epub 2009 Aug 19. Int J Radiat Oncol Biol Phys. 2010. PMID: 19695794 Clinical Trial.
-
Generation and validation of a prognostic score to predict outcome after re-irradiation of recurrent glioma.Acta Oncol. 2013 Jan;52(1):147-52. doi: 10.3109/0284186X.2012.692882. Epub 2012 Jun 11. Acta Oncol. 2013. PMID: 22686472
-
Radiotherapeutic alternatives for previously irradiated recurrent gliomas.BMC Cancer. 2007 Aug 30;7:167. doi: 10.1186/1471-2407-7-167. BMC Cancer. 2007. PMID: 17760992 Free PMC article. Review.
Cited by
-
Factors influencing quality of life in adult patients with primary brain tumors.Neuro Oncol. 2012 Sep;14 Suppl 4(Suppl 4):iv8-16. doi: 10.1093/neuonc/nos205. Neuro Oncol. 2012. PMID: 23095834 Free PMC article. Review.
-
External beam re-irradiation, combination chemoradiotherapy, and particle therapy for the treatment of recurrent glioblastoma.Expert Rev Anticancer Ther. 2016;16(3):347-58. doi: 10.1586/14737140.2016.1143364. Epub 2016 Feb 9. Expert Rev Anticancer Ther. 2016. PMID: 26781426 Free PMC article. Review.
-
Bevacizumab combined with re-irradiation in recurrent glioblastoma.Front Oncol. 2022 Aug 4;12:961014. doi: 10.3389/fonc.2022.961014. eCollection 2022. Front Oncol. 2022. PMID: 36046037 Free PMC article.
-
Hypofractionated stereotactic reirradiation of recurrent glioblastomas : a beneficial treatment option after high-dose radiotherapy?Strahlenther Onkol. 2009 Apr;185(4):235-40. doi: 10.1007/s00066-009-1753-x. Epub 2009 Apr 16. Strahlenther Onkol. 2009. PMID: 19370426 Clinical Trial.
-
Influence of far upstream element binding protein 1 gene on chemotherapy sensitivity in human U251 glioblastoma cells.Arch Med Sci. 2016 Feb 1;12(1):156-62. doi: 10.5114/aoms.2016.57592. Epub 2016 Feb 2. Arch Med Sci. 2016. PMID: 26925132 Free PMC article.
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Medical