Hypofractionated radiotherapy for glioblastoma: therapeutic outcomes, toxicities and quality of life
PO-1139
Abstract
Hypofractionated radiotherapy for glioblastoma: therapeutic outcomes, toxicities and quality of life
Authors: Fatma Dhouib1, Sirine Zouari1, Nejla Fourati1, Mouna Kallel1, Wicem Siala1, Wafa Mnejja1, Jamel Daoud1
1Habib Bourguiba University Hospital, Oncology-radiotherapy, Sfax, Tunisia
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Purpose or Objective
Glioblastoma
(GB) is the most common primary malignant brain tumor in adults. Despite
improvements in survival with aggressive chemoradiation, outcomes remain poor. Though
the literature supports the use of standard radiotherapy (SRT) (60 Gy in 30
fractions), several randomized studies have supported the use of
hypofractionated regimen especially for elderly patients. The aim of this study
was to evaluate the effectiveness and safety of the hypofractionated
radiotherapy (HRT) in patients with GB.
Material and Methods
This is a retrospective study analyzing the data of
37 patients with GB treated between 2016 and 2020. The median age was 60 years
[15-84] (HRT: 72 years; SRT: 66 years) and the performance score (WHO) was ³ 2 in 64% of cases. The median tumor size was 52 mm
[3-9,6]. Adjuvant SRT was performed in 70.3% of cases and HRT (40 Gy in 15
fractions) in 29.7% of cases, depending on age and initial WHO score. Concomitant
and adjuvant Temozolamide was administered in 51.4% of cases (only for patients
treated by SRT). The primary end-point
was the effectiveness of the HRT evaluation by analyzing the overall survival
(OS) and disease-free survival (DFS) rates. Clinical assessment of radiation-induced
toxicities was performed at the end of radiotherapy sessions using a
questionnaire based on the RTOG clinical scales. Assessement of patients
quality of life was based on the EORTC QLQ-BN20 questionnaire.
Results
Median OS was 12 months [5-23] and 6 months
[3-13] respectively for SRT and HRT (p = 0.01). Median DFS was 8 months [1-18] and 2 months [1-6]
respectively for SRT and HRT (p = 0.01). Multivariate analysis showed that OS predictive
factors were the age (age >60 ans; p=0.003), the
WHO score (WHO >=2; p=0.001), the type of adjuvant treatment (RT alone; p<10-3)
and the fractionation regimen (HRT; p=0.001). For DFS, the predictive factors were:
the WHO score (WHO >=2; p=0.004), the
type of adjuvant treatment (RT alone; p=0.007) and the fractionation regimen
(HRT; p=0.006). For older patients (>65 years old), those with larger tumor (>65 mm) or higher
WHO score (>=2) there were no survival rates differences between HRT and SRT neither for OS (p=0.2,p=0.09
and p=0.1 respectively) nor for DFS (p=0.6,p=0.1
and p=0.4 respectively). For
elderly patients, quality of life and acute
radiation-induced toxicities (nausea,vomiting, alopecia and cerebral edema), were
similar between SRT and HRT.
Conclusion
The results of this
study show the non-inferiority of HRT compared to SRT in terms of survival and
disease control outcomes with less radiation-induced toxicities, especially for
older patients and those with poor prognosis factors, maintaining a good quality
of life. It could be a reasonable therapeutic approach in elderly patients with
less favourably prognosis factors.