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Simultaneous CBCT Acquisition During Arc Radiotherapy (SCART)

6. februar 2015 oppdatert av: Sally Falk

Simultaneous Cone Beam Computed Tomography (CBCT) Acquisition During Arc Radiotherapy

The cone beam image is a part of the radiotherapy treatment machine and uses lower energy xrays as the head of the radiotherapy machine moves around the patient in a circle. This takes pictures that give 3-dimensional information, somewhat like a CT scan. These images are better at showing the position of the tumour and surrounding soft tissues than the standard xrays that were previously used. Cone Beam Imaging Technology is not new and has been used regularly at The Christie for many years. The standard cone beam scan is taken before the actual radiotherapy treatment or after the treatment has been delivered.

Volumetric Modulated Arc Therapy (VMAT or Arc Radiotherapy) is a novel method of delivering radiotherapy that involves the continuous movement of the radiotherapy treatment machine head around the patient and MLC during radiation. Arc radiotherapy has been clinically implemented at The Christie for prostate radiotherapy treatments and work is in progress for implementation in lung radiotherapy. The continuous gantry rotation inherent to VMAT delivery makes this simultaneous imaging possible, although there are concerns associated with the impact that this may have on patient dose and image quality.

The aim of this research is to assess whether the image quality of cone beam scans taken during treatment are as good as standard cone beam scans taken before or after treatment used to determine the accuracy of patient position and the tumour coverage by radiotherapy.

Studieoversikt

Status

Ukjent

Studietype

Intervensjonell

Registrering (Forventet)

75

Fase

  • Ikke aktuelt

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiesteder

    • Greater Manchester
      • Manchester, Greater Manchester, Storbritannia, M20 4BX
        • Rekruttering
        • The Christie NHS Foundation Trust
        • Hovedetterforsker:
          • Corinne Faivre-Finn
        • Underetterforsker:
          • Ananya Choudhury
        • Ta kontakt med:

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 for prostate cancer patients:

  • Patients to be treated with radical RT for prostate cancer
  • Patients to be treated with VMAT
  • ECOG performance status 0-2
  • Patients must be able to receive and understand verbal and written information regarding the study and give written, informed consent

Inclusion Criteria for lung cancer patients:

  • A histological or cytological diagnosis of non-small cell lung cancer or small cell lung cancer
  • Patients to be treated with radical RT or SBRT
  • Patients to be treated with VMAT
  • ECOG performance status 0-2
  • Patients must be able to receive and understand verbal and written information regarding the study and give written, informed consent
  • Female patients must meet one of the following criteria - postmenopausal for a minimum of one year, surgically sterile, not pregnant, confirmed by β-HCG blood test and willing to use adequate contraception during study participation, not breastfeeding

Exclusion Criteria for prostate cancer patients:

  • Clinical judgement by the investigator that the patient should not participate in the study
  • Patients in clinical trials of new investigational medicinal products or treatment regimens unless there is written, prior agreement that the patient can also consent to this study, and that clinical data can also be used for this study
  • Prior radiotherapy or surgery in the pelvis that can make identification of normal anatomy difficult

Exclusion criteria for lung cancer patients:

  • Clinical judgement by the investigator that the patient should not participate in the study
  • Patients in clinical trials of new investigational medicinal products or treatment regimens unless there is written, prior agreement that the patient can also consent to this study, and that clinical data can also be used for this study
  • Prior radiotherapy or surgery in the region of interest that can make identification of normal anatomy difficult

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Tildeling: N/A
  • Intervensjonsmodell: Enkeltgruppeoppdrag
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: Cone Beam Computed Tomography
Simultaneous Cone Beam Computed Tomography acquisition during arc radiotherapy.
Simultaneous Cone Beam Computed Tomography acquisition during arc radiotherapy

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Equivalence of image quality
Tidsramme: 12 months
To show equivalence of image quality from simultaneous CBCT acquisition during delivery of arc radiotherapy with that obtained from conventional CBCT acquisition in lung and prostate patients, as assessed by user-questionnaires.
12 months

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Quantify inter-observer variation
Tidsramme: 12 months
To quantify inter-observer variation in interpretation of anatomy, as assessed by questionaires.
12 months
Quantify inter-observer variation
Tidsramme: 12 months
To quantify inter-observer variation in delineation of specific structures on CBCT scans.
12 months
Quantify impact on treatment times.
Tidsramme: 12 months
To quantify the impact of simultaneous CBCT scans on treatment times.
12 months

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Sponsor

Etterforskere

  • Hovedetterforsker: Ananya Choudhury, The Christie NHS Foundation Trust

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

1. juni 2011

Primær fullføring (Forventet)

1. desember 2015

Studiet fullført (Forventet)

1. desember 2015

Datoer for studieregistrering

Først innsendt

22. april 2014

Først innsendt som oppfylte QC-kriteriene

24. april 2014

Først lagt ut (Anslag)

28. april 2014

Oppdateringer av studieposter

Sist oppdatering lagt ut (Anslag)

9. februar 2015

Siste oppdatering sendt inn som oppfylte QC-kriteriene

6. februar 2015

Sist bekreftet

1. februar 2015

Mer informasjon

Begreper knyttet til denne studien

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. .

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