Evaluation of the Efficacy of Hippocampal Avoidance on the Cognitive Toxicity of Whole-Brain Radiation Therapy After Surgical Resection of Single Brain Metastasis of Breast Cancer
Primary Purpose
Breast Cancer, Brain Metastasis
Status
Completed
Phase
Phase 3
Locations
France
Study Type
Interventional
Intervention
Radiation therapy Brain metastasis in breast cancer
Sponsored by
About this trial
This is an interventional treatment trial for Breast Cancer focused on measuring Breast cancer, one brain metastasis
Eligibility Criteria
Inclusion Criteria:
- Age > or equal 18 years old,
- Single brain metastasis from breast cancer, first cerebral event,
- Complete surgical resection of cerebral metastasis,
- Histological confirmation of brain metastasis of breast cancer,
- Start of radiotherapy within 6 weeks after surgery,
- Karnofsky > or equal to 70,
- No history of brain radiotherapy,
- Signed informed consent to participate,
- Patient affiliated to a social security system or benefiting from such a system.
Exclusion Criteria:
- Multiple brain metastases, leptomeningeal metastases,
- macroscopic metastasis surgery not complete,
- Warning signs of brain displacement (uncontrolled oedema),
- History of cerebral irradiation or absence of surgical treatment of the current metastasis,
- History of cancer in the previous 5 years prior to entry in the study, other than cutaneous basal cell carcinoma or in situ epithelioma of uterine cervix or the stated breast cancer,
- MMSE (Mini Mental State Examination)< 24,
- all previous systemic treatments less than 2 weeks are not allowed,
- Pregnant women or liable to become pregnant, lactating women,
- Persons deprived of their freedom or under tutelage
- Patients unable to comply with medical procedures of the study for geographical, social, or psychological reasons.
Sites / Locations
- Agnès TALLET
Arms of the Study
Arm 1
Arm 2
Arm Type
Other
Other
Arm Label
conventional postoperative whole-brain radiation therapy
whole-brain radiation therapy with hippocampal avoidance
Arm Description
conventional postoperative whole-brain radiation therapy (40 Gy in 20 fractions of 2 Gy)
Radiation therapy with hippocampal avoidance
Outcomes
Primary Outcome Measures
To assess cognitive toxicity
Evaluation criteria to assess cognitive toxicity have been selected on the basis of the recommendations from C. Meyers and P. Brown, who propose an adapted test battery to evaluate memory, verbal function, visual and motor coordination, and executive function. The selected tests have been validated, also in French. They comprise HVLT-R (Hopkins Verbal Learning Test Revised), COWAT (Controlled Oral Word Association Test), Grooved Pegboard test, TMT A and B (Trailmaking tests A and B), and MMSE. The calculation of patient numbers was based on the HVLT-R test, as memory is thought to be the most frequently affected domain.
Secondary Outcome Measures
Quality of life
Quality of life : QLQ-C30, QLQ-BN20, ADL, IADL. Intra-cerebral Progression-free survival (PFS) up to 24 months. Overall survival up to 24 months.
Intra-cerebral progression
to assess by RMI or clinical signs
Overall survival
Full Information
NCT ID
NCT01942980
First Posted
September 6, 2013
Last Updated
August 10, 2018
Sponsor
Institut Paoli-Calmettes
1. Study Identification
Unique Protocol Identification Number
NCT01942980
Brief Title
Evaluation of the Efficacy of Hippocampal Avoidance on the Cognitive Toxicity of Whole-Brain Radiation Therapy After Surgical Resection of Single Brain Metastasis of Breast Cancer
Official Title
Double-blind Randomized Multicenter Phase III Study Evaluation of the Efficacy of Hippocampal Avoidance on the Cognitive Toxicity of Whole-brain Radiation Therapy After Surgical Resection of Single Brain Metastasis of Breast Cancer.
Study Type
Interventional
2. Study Status
Record Verification Date
August 2018
Overall Recruitment Status
Completed
Study Start Date
March 2013 (undefined)
Primary Completion Date
March 22, 2016 (Actual)
Study Completion Date
June 6, 2017 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Institut Paoli-Calmettes
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The incidence of brain metastases (BM) in metastatic breast cancer is increasing, due to the improvement in the control of systemic disease, and due to an improved detection through imagery.
The treatment management of single BM remains controversial. Indeed, even though it is widely accepted that local treatment increases the median survival time in patients having a good prognostic status, the adding of "adjuvant" whole-brain radiation therapy (WBRT) is currently subject to controversy, due to its potential toxicity. Yet, two randomized trials have demonstrated a clear increase in intra-cerebral recurrence and in death from neurologic origin in case of absence of "adjuvant" WBRT, without change in overall survival (but overall survival was not a primary endpoint in any of these studies).
The data from literature on cognitive toxicity (CT) of WBRT on BM are scarce and sometimes controversial. CT of WBRT affects the subcortical frontal functions. It is postulated that the alteration of hippocampal neurogenesis (mainly due to inflammation process), situated in the subgranular zone of the dentate gyrus, has an essential role in the development of these brain dysfunctions.
It has been shown that the incidence of BM in the hippocampal region (hippocampus + 5mm expansion) is low, in the range of 8,6%.
New irradiation techniques, in particular intensity-modulated radiotherapy associated with rotational radiotherapy, allow to modulate the dose on an intra-cerebral structure, all the while distributing an adapted dose to the remaining brain.
This prospective, randomized study, will compare, through a battery of neuropsychological tests, the cognitive impact of WBRT of 40 Gy in 20 fractions with or without hippocampal avoidance by intensity modulated radiotherapy, in patients presenting with a single operated brain metastasis of breast cancer. If the hippocampal avoidance leads to a significant improvement in cognitive function, this radiotherapy scheme could become the standard postoperative treatment to be proposed to patients presenting the best prognostic factors. This would allow to prevent long-term cognitive deficit, while preserving WBRT benefit on intra-cerebral control.
Justification of evaluation criteria :
Principal criteria :
Evaluation criteria to assess cognitive toxicity have been selected on the basis of the recommendations from C. Meyers and P. Brown, who propose an adapted test battery to evaluate memory, verbal function, visual and motor coordination, and executive function. The selected tests have been validated, also in French. They comprise HVLT-R (Hopkins Verbal Learning Test Revised), COWAT (Controlled Oral Word Association Test), Grooved Pegboard test, TMT A and B (Trailmaking tests A and B), and MMSE. The calculation of patient numbers was based on the HVLT-R test, as memory is thought to be the most frequently affected domain.
The tests will be performed before treatment ("baseline" cognitive function), at 4 months and at 12 months. In case of a missing answer to the evaluation tests, the reason(s) for not answering will be noted.
Secondary criteria :
Quality of life : QLQ-C30, QLQ-BN20, ADL, IADL Intra-cerebral Progression-free survival (PFS) Overall survival.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Cancer, Brain Metastasis
Keywords
Breast cancer, one brain metastasis
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
8 (Actual)
8. Arms, Groups, and Interventions
Arm Title
conventional postoperative whole-brain radiation therapy
Arm Type
Other
Arm Description
conventional postoperative whole-brain radiation therapy (40 Gy in 20 fractions of 2 Gy)
Arm Title
whole-brain radiation therapy with hippocampal avoidance
Arm Type
Other
Arm Description
Radiation therapy with hippocampal avoidance
Intervention Type
Radiation
Intervention Name(s)
Radiation therapy Brain metastasis in breast cancer
Intervention Description
Radiation
Primary Outcome Measure Information:
Title
To assess cognitive toxicity
Description
Evaluation criteria to assess cognitive toxicity have been selected on the basis of the recommendations from C. Meyers and P. Brown, who propose an adapted test battery to evaluate memory, verbal function, visual and motor coordination, and executive function. The selected tests have been validated, also in French. They comprise HVLT-R (Hopkins Verbal Learning Test Revised), COWAT (Controlled Oral Word Association Test), Grooved Pegboard test, TMT A and B (Trailmaking tests A and B), and MMSE. The calculation of patient numbers was based on the HVLT-R test, as memory is thought to be the most frequently affected domain.
Time Frame
From inclusion/randomization to 12 months
Secondary Outcome Measure Information:
Title
Quality of life
Description
Quality of life : QLQ-C30, QLQ-BN20, ADL, IADL. Intra-cerebral Progression-free survival (PFS) up to 24 months. Overall survival up to 24 months.
Time Frame
At inclusion/randomization, at month 1, month 4 and month 12
Title
Intra-cerebral progression
Description
to assess by RMI or clinical signs
Time Frame
Evaluated every 3 months
Title
Overall survival
Time Frame
up to 24 months
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age > or equal 18 years old,
Single brain metastasis from breast cancer, first cerebral event,
Complete surgical resection of cerebral metastasis,
Histological confirmation of brain metastasis of breast cancer,
Start of radiotherapy within 6 weeks after surgery,
Karnofsky > or equal to 70,
No history of brain radiotherapy,
Signed informed consent to participate,
Patient affiliated to a social security system or benefiting from such a system.
Exclusion Criteria:
Multiple brain metastases, leptomeningeal metastases,
macroscopic metastasis surgery not complete,
Warning signs of brain displacement (uncontrolled oedema),
History of cerebral irradiation or absence of surgical treatment of the current metastasis,
History of cancer in the previous 5 years prior to entry in the study, other than cutaneous basal cell carcinoma or in situ epithelioma of uterine cervix or the stated breast cancer,
MMSE (Mini Mental State Examination)< 24,
all previous systemic treatments less than 2 weeks are not allowed,
Pregnant women or liable to become pregnant, lactating women,
Persons deprived of their freedom or under tutelage
Patients unable to comply with medical procedures of the study for geographical, social, or psychological reasons.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Agnès TALLET, MD
Organizational Affiliation
Institut Paoli-Calmettes
Official's Role
Principal Investigator
Facility Information:
Facility Name
Agnès TALLET
City
Marseille
ZIP/Postal Code
13009
Country
France
12. IPD Sharing Statement
Links:
URL
http://www.institutpaolicalmettes.fr
Description
official web site of the sponsor
Learn more about this trial
Evaluation of the Efficacy of Hippocampal Avoidance on the Cognitive Toxicity of Whole-Brain Radiation Therapy After Surgical Resection of Single Brain Metastasis of Breast Cancer
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