The aim of this study is to demonstrate if it is possible to delivering a novel and modern radiotherapy approach (Dose Escalated internal PTV (DE-iPTV)) and to collect health related quality of life in patients whose breast cancer has spread to the brain (brain metastases) at 8 weeks post enrolling into the study. The main questions that have been set out to to answer are: * Is it possible to deliver the novel radiotherapy approach, DE-iPTV? * Is it possible to measure health -related quality of life? * What impact does the novel radiotherapy approach have on: patient's quality of life, control of the brain metastasis (control of the lesion) and steroid use? Participants will: * Receive 5 doses of radiotherapy * Complete weekly quality of life (EQ-5D) assessments and medication (steroid) diaries (via telephone/ postal) until 12 weeks post enrolment * Be reviewed in clinic with up-to-date MRI scans at 8, 12 and 24 weeks post-enrolment * Complete a more detailed HRQoL panel of assessments will be assessed at baseline, 8 weeks, 12 weeks and 24 weeks post enrolment.
Brain metastases from breast cancer are a common, and devastating, complication with survival times of 3 - 5 months from diagnosis. The main treatment approaches to brain metastases are surgery, stereotactic radiosurgery (SRS), and whole brain radiotherapy. However, it is known that most patients with brain metastases receive either whole-brain radiotherapy (WBRT) or no treatment, with relatively low rates of surgery and SRS. Since the commonest treatment in those who do have treatment is WBRT, the local team have developed an approach that is believed to be (possibly) more effective than WBRT. The objective is to evaluate this approach in patients who are not suitable to receive more aggressive treatment and who would otherwise receive WBRT. The local approach involves using a modern radiotherapy planning approach, combined with careful, intra-metastasis dose escalation (Dose Escalated internal PTV (DE-iPTV)) to deliver a higher dose to tumour, while delivering less dose to the brain. The combination of less dose to normal structures and more dose to the lesion will hopefully improve Health-related Quality of Life (HRQoL). The aim of this study is to demonstrate the feasibility of delivering complex radiotherapy, dose escalated internal PTV (DE-iPTV), and measuring quality of life at 8 weeks post-enrolment for patients with brain metastases from breast cancer who would otherwise receive WBRT. An exploratory blood-based biomarker sample collection and analysis will be completed. Furthermore, linked national cancer data will be used to measure the number of patients currently offered WBRT, including survival costs and hospital admissions, and thus provide a baseline to estimate the impact of this novel approach.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
42
Dose-escalated VMAT-based radiotherapy, as previously described in our planning study
Imperial College London
London, United Kingdom
Feasibility of delivering DE-iPTV and measuring health related quality of life questionnaire in patients with brain metastases from breast cancer to whom their treating clinician would normally offer whole brain radiotherapy
Completion of radiotherapy and completion of EuroQol- 5 Dimension (EQ-5D-5L) questionnaire
Time frame: 8 weeks post-enrolment
Lesional Response
Lesional response and intracranial progression measured using RANO-BM criteria
Time frame: 8 weeks
Intracranial progression
Intracranial progression based on RANO-BM
Time frame: 3 months
Intracranial progression
Intracranial progression based on RANO-BM
Time frame: 6 months
Treatments
Use of further brain-directed therapies (reported by clinician)
Time frame: Within 6 months of enrolment
Central Nervous System (CNS) Failures
Time to CNS failure (either lesional progression or developing a new lesion as per RANO-BM)
Time frame: Within 6 months of enrolment
Neurological toxicities
Acute and late neurological/ CNS toxicity as assessed using CTCAE v5
Time frame: Within 6 months of enrolment
Health Related Quality of Life
HRQoL over time (participants reported outcomes for descriptive analysis)
Time frame: Within 6 months of enrolment
Time to deterioration in quality of life
Time to deterioration in Health Related Quality of Life - measured as time to first time there is a minimum clinically significant change in EuroQol- 5 Dimension (EQ-5D-5L)
Time frame: Within 6 months of enrolment
Symptom Burden
Symptom burden assessed by collection of clinician-recorded toxicities
Time frame: Within 6 months of enrolment
Steroid usage
Use of corticosteroids over time, assessed through clinician reports and patient diaries
Time frame: Within 6 months of enrolment
Quality-Adjusted Life Year
Quality-Adjusted Life Year
Time frame: Within 6 months of enrolment
Overall survival
Overall survival
Time frame: End of study
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