Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02953756
Other study ID # 842003008
Secondary ID
Status Completed
Phase
First received
Last updated
Start date October 2015
Est. completion date October 2019

Study information

Verified date February 2020
Source Elisabeth-TweeSteden Ziekenhuis
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Stereotactic radiosurgery (SRS) is increasingly applied in patients with brain metastases (BM) and is expected to have less adverse effects on cognitive functioning than Whole Brain Radiation Therapy (WBRT). Because cognitive functions are essential for daily functioning, and may affect therapy compliance and quality of life in general, a full understanding of cognitive functioning in patients with BM after SRS is essential.

CAR-Study A is a prospective study to evaluate cognitive functioning in patients with 1-10 BM accepted for treatment with Gamma Knife radiosurgery (GKRS).


Description:

CAR-Study A is a prospective study to evaluate cognitive functioning after GKRS in patients with 1-10 newly diagnosed brain metastases on a triple dose gadolinium-enhanced MRI-scan. Neuropsychological assessment will be performed at baseline and at 3, 6, 9, 12, 15, and 21 months after treatment. Follow-up assessments will be combined with 3-monthly MRI-scans.


Recruitment information / eligibility

Status Completed
Enrollment 92
Est. completion date October 2019
Est. primary completion date October 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Histologically proven malignant cancer

- 1-10 newly diagnosed brain metastases on a triple dose gadolinium-enhanced MRI-scan

- Maximum total tumor volume 30 cm3

- Lesion = 3 mm from the optic apparatus

- Age = 18 years

- Karnofsky Performance Status (KPS) = 70

- Anticipated survival > 3 months

Exclusion Criteria:

- No prior histologic confirmation of malignancy

- Primary brain tumor

- A second active primary tumor

- Small cell lung cancer

- Lymphoma

- Leukemia

- Meningeal disease

- Progressive, symptomatic systemic disease without further treatment options

- Prior brain radiation

- Prior surgical resection of brain metastases

- Additional history of a significant neurological or psychiatric disorder

- Participation in a concurrent study in which neuropsychological testing and/or health-related QOL assessments are involved

- Contra indications to MRI or gadolinium contrast

- Underlying medical condition precluding adequate follow-up

- Lack of basic proficiency in Dutch

- IQ below 85

- Severe aphasia

- Paralysis grade 0-3 according to MRC scale (Medical Research Council)

Study Design


Intervention

Radiation:
Gamma Knife radiosurgery
Gamma Knife radiosurgery will be performed with a Leksell Gamma Knife® Icon, Elekta Instruments, AB. Depending upon the tumor volume, a dose of 18-25 Gy will be prescribed with 99-100% coverage of the target

Locations

Country Name City State
Netherlands Gamma Knife Center Tilburg, Elisabeth-TweeSteden Hospital Tilburg Noord-Brabant

Sponsors (3)

Lead Sponsor Collaborator
Elisabeth-TweeSteden Ziekenhuis University of Tilburg, ZonMw: The Netherlands Organisation for Health Research and Development

Country where clinical trial is conducted

Netherlands, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in verbal memory Verbal memory is measured with the Hopkins Verbal Learning Test-Revised (HVLT-R) Baseline and 3, 6, 9, 12, 15, and 21 months post GKRS
Primary Change in cognitive flexibility Cognitive flexibility is measured with the Trail Making Test B (TMT B) Baseline and 3, 6, 9, 12, 15, and 21 months post GKRS
Primary Change in word fluency Word Fluency is measured with the Controlled Oral Word Association (COWA) Baseline and 3, 6, 9, 12, 15, and 21 months post GKRS
Primary Change in working memory Working memory is measured with the Wechsler Adult Intelligence Scale - Digit Span Baseline and 3, 6, 9, 12, 15, and 21 months post GKRS
Primary Change in processing speed Processing speed is measured with the Wechsler Adult Intelligence Scale - Digit Symbol Baseline and 3, 6, 9, 12, 15, and 21 months post GKRS
Primary Change in motor dexterity Motor dexterity is measured with the Grooved Pegboard (GP) Baseline and 3, 6, 9, 12, 15, and 21 months post GKRS
Secondary Health Related Quality Of Life (HRQOL) The Functional Assessment of Cancer Therapy-Brain (FACT-Br) is used to measure HRQOL. Baseline and 3, 6, 9, 12, 15, and 21 months post GKRS
Secondary Fatigue Fatigue is measured with the Multidimensional Fatigue Inventory (MFI). Baseline and 3, 6, 9, 12, 15, and 21 months post GKRS
Secondary Depression and anxiety Depression and anxiety are measured with the Hospital Anxiety and Depression Scale (HADS). Baseline and 3, 6, 9, 12, 15, and 21 months post GKRS.
Secondary Median Overall Survival Overall survival is defined as the time in months from the start of GKRS to the date of death or last contact if alive. Kaplan-Meier methods are used to estimate overall survival. 12 months after GKRS
Secondary Local tumor control Local brain tumor control of the initial GKRS-treated lesions is defined as a complete, partial, or stable response, or less than a 25% increase in diameter on contrast-enhanced MRI follow-up and not requiring resection. Any initial treated lesions increased by more than 25% in diameter on contrast-enhanced MRI or required resection will be considered a local failure. 12 months after GKRS
Secondary Distant tumor control Distant brain tumor control is defined as the absence of any new brain metastases, distinct from the initial GKRS-treated lesion(s), on follow-up MRI. The appearance of one or more new lesions in the brain by contrast-enhanced follow-up MRI is considered distant failure. 12 months after GKRS
See also
  Status Clinical Trial Phase
Active, not recruiting NCT03911388 - HSV G207 in Children With Recurrent or Refractory Cerebellar Brain Tumors Phase 1
Terminated NCT02565433 - Prospective Assessment of Quality of Life in Patients Treated by Radiosurgery for Brain Metastases (PRAMECE-1302) N/A
Completed NCT00184353 - Clinical MR Spectroscopy of Brain Metastases at 1,5T and 3T. N/A
Recruiting NCT02789371 - Comparing of Modified Wet Suction Technique and Dry Suction Technique for EUS-FNA of Solid Occupying Lesions N/A
Completed NCT01122199 - Study of RAD001 + AMG479 for Patients With Advanced Solid Tumors Phase 1
Terminated NCT01336985 - Safety and Pharmacokinetics of Treating Liver Cancer With Drug-Eluting Beads Phase 1
Recruiting NCT05419518 - Palliative Dose Escalated Radiation for Painful Non-Spine Bone Metastases and Painful Non-Bone Metas Phase 2
Completed NCT02808416 - Personalized Cellular Vaccine for Brain Metastases (PERCELLVAC3) Phase 1
Completed NCT00668382 - Evaluate The Toxicity And Feasibility Of Intra-Tumoral Injection Phase 1
Completed NCT00152906 - Stereotactic Radiotherapy (SRT) Liver (COLD 1) Phase 1/Phase 2
Completed NCT01267084 - A Study to Assess the Potential Effects of Ketoconazole on the Pharmacokinetics of Trabectedin in Patients With Advanced Malignancies Phase 1/Phase 2
Recruiting NCT02327065 - Prospective Multi-center, Single Blinded, Randomized, Controlled Trial of EUS-FNB and EUS-FNA on Solid Occupying Lesion N/A
Completed NCT02382653 - Oral Piroxicam Versus Buccal Fentanyl in Breakthrough Pain N/A
Completed NCT01273480 - A Study to Assess the Potential Effects of Rifampin on the Pharmacokinetics of Trabectedin in Patients With Advanced Malignancies Phase 1
Completed NCT01273493 - A Pharmacokinetic Study of Trabectedin in Patients With Advanced Malignancies and Hepatic Dysfunction Phase 1
Completed NCT00556049 - Combination Sunitinib and Gemcitabine in Sarcomatoid and/or Poor-risk Patients With Metastatic Renal Cell Carcinoma Phase 2
Recruiting NCT02246634 - Screening for Synchronous Metastases in Colorectal Cancer With DW-MRI (SERENADE) N/A
Terminated NCT01970644 - Neurocognition After Gamma Knife Radiosurgery for Multiple Brian Metastases N/A