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Clinical Trials/NCT03626818
NCT03626818
Unknown
Not Applicable

The Impact of Neurocognitive Function in Patients With Multiple Brain Metastases Receiving Whole Brain Radiation Therapy

Guangdong Association of Clinical Trials1 site in 1 country125 target enrollmentAugust 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Brain Metastases
Sponsor
Guangdong Association of Clinical Trials
Enrollment
125
Locations
1
Primary Endpoint
Delayed recall deterioration rate(HVLT-R)
Last Updated
7 years ago

Overview

Brief Summary

Brain metastases (BM), occurring in 10-30% of adult cancer patients, are an important cause of morbidity and mortality.The prognosis of patients with BM is generally poor, with a median survival time of 2-6 months. Whole-brain radiation therapy (WBRT) has been advocated as the primary treatment for metastatic brain cancer. WBRT injures small cerebral vasculature and neuropil,effects linked to imaging-defined white matter changes. However, information on the neurocognitive function(NCF) impact of WBRT in BM patients is also limited.This study aims to explore and evaluate the impact of NCF in patients with multiple brain metastases receiving WBRT.

Detailed Description

Brain metastases (BM), occurring in 10-30% of adult cancer patients, are an important cause of morbidity and mortality.The prognosis of patients with BM is generally poor, with a median survival time of 2-6 months. Whole-brain radiation therapy (WBRT) has been advocated as the primary treatment for metastatic brain cancer. WBRT injures small cerebral vasculature and neuropil,effects linked to imaging-defined white matter changes. However, information on the neurocognitive function(NCF) impact of WBRT in BM patients is also limited.This study aims to explore and evaluate the impact of NCF in patients with multiple brain metastases receiving WBRT.All patients were assessed at each visit for NCF according to the Hopkins Verbal Learning Test-Revised(HVLT-R),Mini-Mental Status Examination(MMSE) and Quality Of Life measurements(QOL,Questionnaire-QLQC30) .

Registry
clinicaltrials.gov
Start Date
August 2018
End Date
June 2021
Last Updated
7 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Pathologically proven solid tumor malignancy.
  • Brain MRI within 1 month of enrolment, at least three metastatic lesions in the brain (of which at least one had to be measurable according to Response Evaluation Criteria in Solid Tumors \[RECIST\], version 1.1).
  • Males or females aged ≥18 years, \< 75 years.
  • had an Eastern Cooperative Oncology Group (ECOG) performance-status score from 0 to
  • A life expectancy of at least 3 months.
  • Adequate organ function according to the National Cancer Institute Common Terminology Criteria for Adverse Events (NCI-CTCAE) version 4.0
  • Subjects did not receive other treatments such as cytotoxic drugs, radiotherapy (non-brain metastases) or surgery within 2 weeks.
  • Patients must have ability and general health that permits completion of the study requirements and required follow up.
  • Patients must be willing to complete NCF and QOL assessments at pre-specified time points outlined in the protocol.
  • Signed written informed consent

Exclusion Criteria

  • Prior radiation therapy to the brain.
  • Radiologically or pathologically confirmed metastases in the spinal cord or meninges.
  • Taking sedatives and hypnotics, phenytoin, carbamazepine, rifampin, and barbiturate.
  • Any unstable systemic disease (including active infection, uncontrolled hypertension, unstable angina, hepatic, renal, or metabolic disease).
  • Subjects suffered from dementia, mental illness and other serious cognitive dysfunction.
  • 6.The patient's brain radiation dose needs to be increased. 7.Inability to comply with protocol or study procedures. 8.A serious concomitant systemic disorder that, in the opinion of the investigator, would compromise the patient's ability to complete the study.
  • 9.Pregnant female. 10.Breast-feeding

Outcomes

Primary Outcomes

Delayed recall deterioration rate(HVLT-R)

Time Frame: At 6 month

Secondary Outcomes

  • Change in delayed recall(HVLT-R)(At 6th week, 3rd, 9th, 12th month)
  • Overall survival for patients with different GPA scores(At baseline,6th week, 3rd, 6th, 9th, 12th month, and every 6 months until PS> 2 or intracranial tumor progression)
  • Intracranial progression-free survival for patients with different Graded Prognostic Assessment scores(At baseline,6th week, 3rd, 6th, 9th, 12th month, and every 6 months until Performance Status> 2 or intracranial tumor progression)
  • Change in recall(HVLT-R)(At 6th week, 3rd, 6th, 9th, 12th month)
  • Change score(QLQBN20)(At 6th week, 3rd, 6th, 9th, 12th month)
  • Change score(MMSE)(At 6th week, 3rd, 6th, 9th, 12th month)

Study Sites (1)

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