WBRTvsSRS: Whole Brain Radiotherapy (WBRT) Versus Stereotactic Radiosurgery (SRS) for 4 Upto 10 Brain Metastases

Sponsor
Maastricht Radiation Oncology (Other)
Overall Status
Terminated
CT.gov ID
NCT02353000
Collaborator
(none)
31
7
2
41
4.4
0.1

Study Details

Study Description

Brief Summary

Recently stereotactic radiosurgery (SRS) in 5 up to 10 brain metastases showed to have equal survival as in 2 up to 4 brain metastases. Whole brain radiotherapy (WBRT) is currently the gold standard for patients with more than 3 brain metastases, but has significant side effects. In this prospective randomized phase III trial WBRT is compared to SRS for patients with 4 up to 10 BM.

Condition or Disease Intervention/Treatment Phase
  • Radiation: Stereotactic Radiosurgery
  • Radiation: Whole Brain Radiotherapy
N/A

Detailed Description

Dutch guideline advices stereotactic radiosurgery (SRS) for patients with 1 up to 3 brain metastases (BM) and whole brain radiotherapy (WBRT) for patients with 4 or more BM. The interim analysis from the QUARTZ study showed that WBRT did not provide benefit in quality of life nor survival over best supportive care. WBRT has significant side effects, such as hair loss, fatigue, and cognitive dysfunction which may impair quality of life. A recently published study showed that SRS in patients with 5 up to 10 BM had a comparable survival to patients treated with 2 up to 4 BM. Many systemic therapies do not have a satisfactory intracranial response, because of the blood-brain barrier. The potential advantages of SRS i.e, limiting radiation doses to the uninvolved brain and a high rate of local tumour control by just a single treatment. Next logic step would be to compare WBRT with SRS alone in patients with 4-10 BM and evaluate whether SRS is superior to WBRT with regard to QOL.

Study Design

Study Type:
Interventional
Actual Enrollment :
31 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Whole Brain Radiotherapy vs. Stereotactic Radiosurgery for 4 - 10 Brain Metastases:a Phase III Randomized Multicenter Trial
Study Start Date :
Jul 1, 2016
Actual Primary Completion Date :
Apr 1, 2019
Actual Study Completion Date :
Dec 1, 2019

Arms and Interventions

Arm Intervention/Treatment
Experimental: Stereotactic Radiosurgery

Stereotactic Radiosurgery for patients with 4 up to 10 brain metastases:

Radiation: Stereotactic Radiosurgery
Stereotactic Radiosurgery for patients with 4 up to 10 brain metastases

Other: Whole Brain Radiotherapy

Whole Brain Radiotherapy for patients with 4 up to 10 brain metastases:

Radiation: Whole Brain Radiotherapy
Whole Brain Radiotherapy for patients with 4 up to 10 brain metastases

Outcome Measures

Primary Outcome Measures

  1. Quality of life in patients with 4 - 10 brain metastases comparing WBRT and SRS [Change in quality of life measured from baseline to 3 months after radiotherapy]

    Quality of life is measured by the EQ-5D-5L, a descriptive system of health-related quality of life states consisting of five dimensions (mobility, self-care, usual activities, pain/discomfort, anxiety/depression)

Secondary Outcome Measures

  1. Overall survival steroid use (mg), toxicity including hair loss and fatigue. [1 year]

    Overall survival

  2. Time that patient is functioning independently (Karnofsky ≥ 70) [Change in Karnofsky index from baseline to 3 months after radiotherapy]

    Time that patient is functioning independently (Karnofsky ≥ 70)

  3. Steroid use [Change in steroid use from baseline to 3 months after radiotherapy]

    Steroid use in mg over time

  4. Toxicity measured by hair loss and fatigue [Change in toxicity from baseline to 3 months after radiotherapy]

    Toxicity measured by hair loss and fatigue using CTCAE version 4.0

  5. Degree of independence [Change in independence from baseline to 3 months after radiotherapy]

    Degree of independence of patients using the Barthel index

Other Outcome Measures

  1. Brain salvage during follow-up [1 year]

    Brain salvage during follow-up, type of salvage, and time to salvage after randomisation

  2. Verbal learning [Change in verbal recall and verbal recognition from baseline to 3 months after radiotherapy]

    Verbal recall and verbal regognition is measured using the Hopkins Verbal Learning Test - Revised

  3. Quality of life of cancer patients [Change in Quality of life from baseline to 3 months after radiotherapy]

    QoL will be measured using the EORTC QLQ-C30

  4. Quality of life of cancer patients with brain neoplasms [Change in Quality of life from baseline to 3 months after radiotherapy]

    QoL will be measured using the EORTC QLQ-BN20

  5. Quality of life of cancer patients measuring cancer-related fatigue [Change in Quality of life from baseline to 3 months after radiotherapy]

    QoL will be measured using the EORTC QLQ-FA13

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Minimal 4 up to a maximum of 10 BM on diagnostic MRI scan

  • Max diameter of single GTV 2.5cm

  • Max cumulative GTV of 30cm3

  • Karnofsky performance status ≥ 70

  • Any solid primary tumour. Small cell lung carcinoma, germinoma, and lymphoma are excluded

  • Ability to provide written informed consent

Exclusion Criteria:
  • Contra-indication for MRI

  • Prior treatment for BM (i.e. surgery, SRS or WBRT)

  • Concurrent use of systemic therapy

  • Maximum cumulative GTV of more than 30cm3 on planning-MRI

  • More than 10 BM on planning-MRI

  • A brainstem metastasis with a PTV of more than 20 cm3

Contacts and Locations

Locations

Site City State Country Postal Code
1 VUmc Amsterdam Netherlands 1081HV
2 AMC Amsterdam Netherlands 1105AZ
3 Haaglanden MC Den Haag Netherlands 2262BA
4 Maastricht Radiation Oncology (MAASTRO clinic) Maastricht Netherlands 6202 AZ
5 Erasmus MC Rotterdam Netherlands 3015CE
6 Instituut Verbeeten Tilburg Netherlands 5042BS
7 ZRTI Vlissingen Netherlands 4382EK

Sponsors and Collaborators

  • Maastricht Radiation Oncology

Investigators

  • Principal Investigator: Philippe Lambin, Prof. Dr., Maastro Clinic, The Netherlands

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Maastricht Radiation Oncology
ClinicalTrials.gov Identifier:
NCT02353000
Other Study ID Numbers:
  • 01-2015
First Posted:
Feb 2, 2015
Last Update Posted:
Jun 1, 2020
Last Verified:
May 1, 2020
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 1, 2020