Local Radiotherapy Following Complete Resection of a Brain Metastasis
17. mai 2019 oppdatert av: Anna Bruynzeel, Amsterdam UMC, location VUmc
Postoperative Local Stereotactic Radiotherapy Versus Observation Following a Complete Resection of a Single Brain Metastasis
Objective: To improve local control following complete resection of a single brain metastasis using fractionated local stereotactic radiotherapy, whilst maintaining neurological functioning, neurocognition and quality of life.
Study design: Multicenter randomized phase III, with at least three high-volume Dutch centers participating in the trial. Stratification on primary tumor type and age.
Study population: Patients undergoing complete resection of a single brain metastasis, confirmed by an early (i.e. within 72 hours) postoperative contrast-enhanced MR scan.
Study intervention: Patients will be randomized between observation alone (standard arm) and local stereotactic radiotherapy in three fractions of 8 Gy to the surgical cavity (study arm).
Main study parameters: Primary objective: local control rate at 6 months. Secondary objectives: local control rate at 12 months, neurological functioning, freedom from clinical neurological progression, performance status, quality of life, toxicity, steroid use, neurocognition and overall survival.
Studieoversikt
Detaljert beskrivelse
The objective of this study is to improve local control following complete resection of a single brain metastasis of solid tumors using fractionated local stereotactic radiotherapy, whilst maintaining neurological functioning, neurocognition and quality of life.
The study is performed in the form of a multicenter randomized phase III, with at least three high-volume Dutch centers participating in the trial.
Stratification will be performed on primary tumor type and age.
A total of 70 patients will be included.
Inclusion is restricted to patients who underwent a complete resection of a single brain metastasis, confirmed by an early (i.e.
within 72 hours) postoperative contrast-enhanced magnetic resonance (MR) scan.
Patients will be randomized between observation alone (standard arm) and local stereotactic radiotherapy in three fractions of 8 Gy to the surgical cavity (study arm).The main study parameters are: local control rate at 6 months (primary outcome measure) and local control rate at 12 months, neurological functioning, freedom from clinical neurological progression, performance status, quality of life, toxicity, steroid use, neurocognition and overall survival (secondary outcome measures).
Follow up will be performed at three-monthly interval during the first two years, including MRI scans.
Quality of life questionaires and neurocognitive functioning tests will be performed at fixed intervals during follow-up.
Studietype
Intervensjonell
Registrering (Faktiske)
70
Fase
- Ikke aktuelt
Kontakter og plasseringer
Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.
Studiesteder
-
-
-
Amsterdam, Nederland, 1066CX
- Netherlands Cancer Institute - Antoni van Leeuwenhoek
-
Amsterdam, Nederland, 1081HV
- VU University Medical Center
-
-
Deltakelseskriterier
Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
18 år og eldre (Voksen, Eldre voksen)
Tar imot friske frivillige
Nei
Kjønn som er kvalifisert for studier
Alle
Beskrivelse
Inclusion Criteria:
- Age of 18 years or older.
- Radiologically confirmed complete resection of a single brain metastasis on a contrast-enhanced MRI within 72 h after resection.
- Primary solid tumor, excluding hematologic malignancy, germ cell tumor, small cell lung cancer.
- Stable extracranial tumor (primary tumor and/or systemic metastases) during the last three months with or without treatment or progressive extracranial tumor and/or systemic metastases for which effective treatment is available.
- World Health Organization (WHO) performance score 0-2.
- Ability to provide written informed consent.
Exclusion Criteria:
- Prior treatment for brain metastases (i.e. surgery, stereotactic radiotherapy or WBRT).
- Distant brain metastases or radiological findings on MRI suspected for leptomeningeal tumor spread on the postoperative MRI.
- Concurrent use of systemic therapy during local stereotactic radiotherapy
Studieplan
Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: Randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Ingen (Open Label)
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
|
Ingen inngripen: observation
Watchful waiting
|
|
|
Aktiv komparator: local stereotactic radiotherapy (SRT)
local SRT in three fractions of 8 Gy to the surgical cavity
|
local stereotactic radiotherapy in three fractions of 8 Gy to the surgical cavity
Andre navn:
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
local control rate
Tidsramme: at 6 months
|
as assessed on follow-up MRI scans
|
at 6 months
|
Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Decrease in neurocognitive test results using the Hopkins Verbal Learning Test Revised (HVLT-R), in full cohorts
Tidsramme: baseline, at 3 months, 6 months and 12 months
|
Neurocognitive testing will be performed at baseline, at three, six and twelve months follow-up using the Hopkins Verbal Learning Test Revised (HVLT-R).
The HVLT-R is one of the components used to form the core set of cognitive tests recommended to use in oncology trials.
This test measures immediate memory span, provides a learning curve, measures both short-term and longer-term retention, and allows for a comparison between retrieval efficiency and learning.
This version includes 3 learning trials of a 12-word list, an interval of 20 minutes a delayed recall, and a recognition trial consisting of the target words interspersed with distractor words.
The score on the recognition trial is the total number of correct response.
This measure has adequate psychometric properties and 6 multiple forms.
|
baseline, at 3 months, 6 months and 12 months
|
|
Decrease in specified neurocognitive test results using the Trail Making A and B, in full cohorts
Tidsramme: baseline, at 3 months, 6 months and 12 months
|
Neurocognitive testing will be performed at baseline, at three, six and twelve months follow-up using the Trail Making A and B. This test is one of the components used to form the core set of cognitive tests recommended to use in oncology trials.
This is a test of visual conceptual and visuomotor tracking.
It measures psychomotor speed and aspects of executive function.
It is given in two parts, A and B. The subject must first draw lines to connect consecutively numbered circles on one work sheet (part A) and then connect the same number of consecutively numbered and lettered circles on another worksheet by alternating between the two sequences (part B).
The subject is urged to connect the circles as fast as possible
|
baseline, at 3 months, 6 months and 12 months
|
|
Decrease in neurocognitive test results using the Controlled Oral Word Association (COWA), in full cohorts
Tidsramme: baseline, at 3 months, 6 months and 12 months
|
Neurocognitive testing will be performed at baseline, at three, six and twelve months follow-up using the Controlled Oral Word Association (COWA).
The COWA is one of the components used to form the core set of cognitive tests recommended to use in oncology trials.
This test measures speeded verbal fluency and aspects of executive function.
In this test, subjects are asked to generate as many words as possible in 1 minute beginning with "B", "D," and "H".
It has two forms.
|
baseline, at 3 months, 6 months and 12 months
|
|
Decrease in neurocognitive test results using using the Wechsler Adult Intelligence Scale (WAIS) III Digit Span and WAIS III Digit Symbol, in full cohorts
Tidsramme: baseline, at 3 months, 6 months and 12 months
|
Neurocognitive testing will be performed at baseline, at three, six and twelve months follow-up using the WAIS III Digit Span and WAIS III Digit Symbol. These added cognitive tests are also chosen based on their proven sensitivity to measure change in neuro-oncology patients. The subtest of the WAIS-III (Digit Span) involves forward and backward repetitions of series of digits and provides measures of concentration. This measure has adequate psychometric properties. The subtest of the WAIS III (Digit Symbol) involves a symbol substitution task that requires visual-motor coordination, motor persistence, and sustained attention. The test is used as a test for information processing speed. The task consists of pairing numbers to nonsense symbols as quickly as possible. |
baseline, at 3 months, 6 months and 12 months
|
|
Decrease in neurocognitive test results using the Grooved Pegboard, in full cohorts
Tidsramme: baseline, at 3 months, 6 months and 12 months
|
Neurocognitive testing will be performed at baseline, at three, six and twelve months follow-up using the Grooved Pegboard.
This added cognitive test is also chosen based on its proven sensitivity to measure change in neuro-oncology patients.
This test measures motor speed and dexterity and is an adjusted version of the Purdue Pegboard test.
The test consists out of plywood with 2 columns of 30 holes and a zinced bowl filled with metal pegs above each column.
Subjects are offered one minute to put as many pegs as possible into the holes.
The test has two different trials: dominant hand only and non-dominant hand only.
|
baseline, at 3 months, 6 months and 12 months
|
Samarbeidspartnere og etterforskere
Det er her du vil finne personer og organisasjoner som er involvert i denne studien.
Sponsor
Studierekorddatoer
Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.
Studer hoveddatoer
Studiestart (Faktiske)
1. mai 2015
Primær fullføring (Faktiske)
1. mai 2017
Studiet fullført (Faktiske)
1. mai 2017
Datoer for studieregistrering
Først innsendt
19. februar 2016
Først innsendt som oppfylte QC-kriteriene
31. mars 2016
Først lagt ut (Anslag)
6. april 2016
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
20. mai 2019
Siste oppdatering sendt inn som oppfylte QC-kriteriene
17. mai 2019
Sist bekreftet
1. mai 2019
Mer informasjon
Begreper knyttet til denne studien
Nøkkelord
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- NL5128302914
Plan for individuelle deltakerdata (IPD)
Planlegger du å dele individuelle deltakerdata (IPD)?
NEI
Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .