Abstract 603P
Background
Glioblastoma is a malignant brain tumour with a high recurrence rate following stanadard first-line treatment. While there are currently guidelines from NICE and EANO on the postoperative surveillance intervals for these patients, they were not evidence-based, and the quality of such recommendations remains untested. We therefore set out to provide an evidence-based recommendation on the optimal postoperative radiological surveillance schedule for glioblastoma patients after surgical treatment, tailored based on the extent of surgical resection and completion of adjuvant treatment.
Methods
This was a territory-wide, multicentre retrospective analysis of consecutive adult patients with IDH-wildtype glioblastoma treated with surgery and radiotherapy (RT) across seven neurosurgical units in Hong Kong between 2006-2020 (n=228). Data were extracted from the Hong Kong Glioblastoma Registry (HK-GBM Registry). Interval-censored Kaplan-Meier curves were constructed for the stratified groups based on the event-free survival of included patients, defined as time from the start date of RT to the occurrence of any event (tumour progression or death). A piecewise exponential model with different hazard functions in predefined time intervals was used to describe each curve. Accordingly, adopting a 15% event rate criterion, we generated the surveillance schedules.
Results
For a 15% event yield each scan (15% event rate criterion), we propose that glioblastoma patients treated with gross total resection be monitored with MRIs around every 9 weeks until 86 weeks after starting RT. Meanwhile, patients with residual tumour after surgery should be monitored more frequently at every 7 weeks until 75 weeks after RT initiation; and the interval should be further shortened to every 4 weeks for patients who were unable to complete the standard 6-weeks concurrent chemoradiotherapy.
Conclusions
Radiological surveillance is an important tool to detect postoperative tumour progression. The extent of surgical resection and completion of adjuvant treatment are major factors associated with glioblastoma progression and the frequency of radiological surveillance should therefore be guided by these two factors.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
The Hong Kong Neuro-oncology Society.
Funding
Has not received any funding.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
62P - Combination of chemotherapy with endocrinal therapy as upfront treatment of metastatic breast cancer in hormone receptor- positive, HER2 -negative disease: A phase II randomised clinical trial
Presenter: Mariam Saleh
Session: Poster Display
Resources:
Abstract
63P - Efficacy and safety of eribulin plus carboplatin combination for HER2-negative metastatic breast cancer
Presenter: Mengqian Ni
Session: Poster Display
Resources:
Abstract
64P - Unmet needs following metastatic breast cancer in a middle-income Asian country
Presenter: Nirmala Bhoo-Pathy
Session: Poster Display
Resources:
Abstract
66P - Utidelone-based therapy in metastatic solid tumors after failure of standard therapies: A prospective, multicenter, single-arm trial
Presenter: Jianjun Zhang
Session: Poster Display
Resources:
Abstract
67P - Efficacy and safety of trastuzumab biosimilar in HER2+ve metastatic breast cancer: A multicenter phase III study
Presenter: krishna Mohan
Session: Poster Display
Resources:
Abstract
68P - Neratinib in combination with fulvestrant and or palbociclib can overcome endocrine resistance in HER2-low/ ER+ breast cancer
Presenter: Maryam Arshad
Session: Poster Display
Resources:
Abstract
69P - A multicenter, retrospective, real-world study of inetetamab combined with pyrotinib and vinorelbine as treatment for HER2-positive metastatic breast cancer
Presenter: Nan Jin
Session: Poster Display
Resources:
Abstract
70P - Overall survival of eribulin, trastuzumab, and pertuzumab as first-line therapy for patients with HER2-positive metastatic breast cancer: A phase II, single-arm clinical trial
Presenter: Kenichi Inoue
Session: Poster Display
Resources:
Abstract
71P - Efficacy and safety of disitamab vedotin after trastuzumab for HER2 -positive breast cancer: A real-world data of retrospective study
Presenter: Chao Li
Session: Poster Display
Resources:
Abstract
72P - Real-world data on the efficacy of T-DM1 biosimilar for the treatment of HER2-positive metastatic breast cancer patients: Outcomes from a single center retrospective study in India
Presenter: Kaushal Patel
Session: Poster Display
Resources:
Abstract