Clinical Trials Logo

Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT02953717
Other study ID # 842003006
Secondary ID NTR5463
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date February 2016
Est. completion date December 2023

Study information

Verified date May 2023
Source Elisabeth-TweeSteden Ziekenhuis
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Whole Brain Radiation Therapy (WBRT) has long been the mainstay of treatment for patients with multiple brain metastases (BM). Meanwhile, Gamma Knife radiosurgery (GKRS) has been increasingly employed in the management of multiple BM to spare healthy tissue. Hence, GKRS is expected to cause fewer cognitive side effects than WBRT. Treatment of multiple BM without cognitive side effects is becoming more important, as more patients live longer due to better systemic treatment options. There are no published randomized trials yet directly comparing GKRS to WBRT in patients with multiple BM, including objective neuropsychological testing. CAR-Study B is a prospective randomized trial comparing cognitive outcome after GKRS or WBRT in eligible patients with 11-20 BM.


Description:

CAR-Study B is a prospective randomized trial comparing cognitive outcome after GKRS or WBRT in eligible patients with 11-20 BM on a triple dose gadolinium-enhanced MRI-scan. Neuropsychological assessment will be performed at baseline and at 3, 6, 9, 12 and 15 months after treatment. Follow-up assessments will be combined with 3-monthly MRI-scans. Patients will be randomized to either GKRS or WBRT. Groups will be balanced at baseline (prior to radiotherapy), taking into account several (stratification) factors that may influence cognitive functioning over time, such as: total tumor volume in the brain, systemic treatment, KPS, age, histology, and baseline HVLT-R total recall score.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 81
Est. completion date December 2023
Est. primary completion date July 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Histologically proven malignant cancer - 11-20 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 (SCLC) - Lymphoma - Leukemia - Meningeal disease - Progressive, symptomatic systemic disease without further treatment options - Prior brain radiation - Prior surgical resection of BM - Cardiovascular accident (CVA) < 2 years ago - Additional history of a significant neurological or psychiatric disorder - Contra indications to MRI or gadolinium contrast - Underlying medical condition precluding adequate follow-up - Participation in a concurrent study in which neuropsychological testing and/or health-related QOL assessments are involved - Lack of basic proficiency in Dutch - IQ below 85 - Severe aphasia - Paralysis grade 0-3 according to MRC scale (Medical Research Council)

Study Design


Related Conditions & MeSH terms


Intervention

Radiation:
Gamma Knife radiosurgery
GKRS is performed with a Leksell Gamma Knife® Icon, Elekta Instruments, AB. Depending upon the volume, a dose of 18-25 Gy will be prescribed with 99-100% coverage of the target.
Whole Brain Radiation Therapy
Patients in the WBRT group will receive 4 Gy x 5 fractions (total of 20 Gy) in one week, which is a commonly utilized treatment schedule according to Dutch guidelines.

Locations

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

Sponsors (3)

Lead Sponsor Collaborator
Elisabeth-TweeSteden Ziekenhuis Tilburg University, 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 Cognitive decline at 3 months Cognitive decline is defined as a significant decline (5 point decrease from baseline based on the Reliable Change Index (RCI) with correction for practice effects) in HVLT-R Total Recall score (verbal learning and memory test) after treatment with either GKRS or WBRT in patients with 11-20 brain metastases at time of treatment initiation. 3 months
Secondary Verbal memory Verbal memory is measured with the Hopkins Verbal Learning Test-Revised (HVLT-R) Baseline and 3, 6, 9, 12 and 15 months post GKRS/WBRT
Secondary Cognitive flexibility Cognitive flexibility is measured with the Controlled Oral Word Association (COWA) Baseline and 3, 6, 9, 12 and 15 months post GKRS/WBRT
Secondary Word Fluency Word Fluency is measured with the Controlled Oral Word Association (COWA) Baseline and 3, 6, 9, 12 and 15 months post GKRS/WBRT
Secondary Working memory Working memory is measured with the Wechsler Adult Intelligence Scale - Digit Span Baseline and 3, 6, 9, 12 and 15 months post GKRS/WBRT
Secondary Processing speed Processing speed is measured with the Wechsler Adult Intelligence Scale - Digit Symbol Baseline and 3, 6, 9, 12 and 15 months post GKRS/WBRT
Secondary Motor dexterity Motor dexterity is measured with the Grooved Pegboard (GP) Baseline and 3, 6, 9, 12 and 15 months post GKRS/WBRT
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 and 15 months post GKRS/WBRT
Secondary Fatigue Fatigue is measured with the Multidimensional Fatigue Inventory (MFI). Baseline and 3, 6, 9, 12 and 15 months post GKRS/WBRT
Secondary Depression and anxiety Depression and anxiety are measured with the Hospital Anxiety and Depression Scale (HADS). Baseline and 3, 6, 9, 12 and 15 months post GKRS/WBRT
Secondary Median Overall Survival Overall survival is defined as the time in months from the start of treatment to the date of death or last contact if alive. Kaplan-Meier methods are used to estimate overall survival. 12 months after GKRS/WBRT
Secondary Local tumor control Local brain tumor control of the initial 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/WBRT
Secondary Distant tumor control Distant brain tumor control is defined as the absence of any new brain metastases, distinct from the initial 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/WBRT
See also
  Status Clinical Trial Phase
Withdrawn NCT06057636 - Hypnosis for Pain in Black Women With Advanced Breast Cancer: A Feasibility Study N/A
Terminated NCT03166631 - A Trial to Find the Safe Dose for BI 891065 Alone and in Combination With BI 754091 in Patients With Incurable Tumours or Tumours That Have Spread Phase 1
Terminated NCT01441115 - ECI301 and Radiation for Advanced or Metastatic Cancer Phase 1
Active, not recruiting NCT03775980 - CIRSE Emprint Microwave Ablation Registry
Completed NCT01114958 - Pilot Study of Intra-Arterial Cisplatin With IV Thiosulfate in Patients With Lung Cancer or Lung Metastases Phase 1
Terminated NCT03986593 - Cryoablation of Bone Metastases From Endocrine Tumors N/A
Active, not recruiting NCT04458259 - Study of PF-07265807 in Participants With Metastatic Solid Tumors. Phase 1
Completed NCT01218542 - Whole Brain Radiation Therapy With Boost to Metastatic Tumor Volume Using RapidArc N/A
Not yet recruiting NCT03175146 - A Study to See Whether Stereotactic Body RadioTherapy (SBRT) Can Shrink Tumours Within the Liver Safely N/A
Active, not recruiting NCT02395224 - A Longitudinal Study of Colorectal Cancer Patients With Metastatic Disease in Middle-Norway
Completed NCT02374411 - Knowledge, Attitudes, and Practice of Surgeons Toward Nutrition Support in HIPEC Patients N/A
Recruiting NCT01960829 - Everolimus in Selected Patients With Metastatic Melanoma: Efficacy and Safety Study Phase 2
Completed NCT01933789 - Improving Communication About Serious Illness N/A
Terminated NCT01846429 - Oral Bicarbonate as Adjuvant for Pain Reduction in Patients With Tumor Related Pain Phase 1
Recruiting NCT01564810 - Cetuximab in Combination With Chemotherapy for the Treatment of Metastatic Colorectal Cancer Phase 4
Completed NCT00375245 - Rapamycin With Grapefruit Juice for Advanced Malignancies Phase 1
Completed NCT00207116 - An Exploratory Pharmacogenomic Study of Monotherapy Erbitux in Subjects With Metastatic Non Small Cell Lung Carcinoma Phase 1
Completed NCT00232726 - Clinical Study of Previously Untreated Patients With Malignant Melanoma Phase 2
Completed NCT00172003 - Effect of Zoledronic Acid in Patients With Renal Cell Cancer and Bone Metastasis Phase 4
Completed NCT00207103 - MAD in Cancer Patients: Safety of BMS-582664 in Patients With Advanced or Metastatic Solid Tumors Phase 1