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PROstate Multicentre External beam radioTHErapy Using a Stereotactic boost: the PROMETHEUS study protocol.
Richardson, Matthew; Sidhom, Mark; Gallagher, Sarah; Grand, Mel; Pryor, David; Bucci, Joseph; Wilton, Lee; Arumugam, Sankar; Keats, Sarah; Martin, Jarad M.
Afiliação
  • Richardson M; Calvary Mater Newcastle, Newcastle, NSW, Australia.
  • Sidhom M; Liverpool and Macarthur Cancer Therapy Centres, Sydney, NSW, Australia.
  • Gallagher S; Calvary Mater Newcastle, Newcastle, NSW, Australia.
  • Grand M; Liverpool and Macarthur Cancer Therapy Centres, Sydney, NSW, Australia.
  • Pryor D; Ingham Institute, Liverpool, NSW, Australia.
  • Bucci J; Princess Alexandra Hospital, Brisbane, QLD, Australia.
  • Wilton L; St. George Hospital Cancer Centre, Sydney, NSW, Australia.
  • Arumugam S; Calvary Mater Newcastle, Newcastle, NSW, Australia.
  • Keats S; Liverpool and Macarthur Cancer Therapy Centres, Sydney, NSW, Australia.
  • Martin JM; Liverpool and Macarthur Cancer Therapy Centres, Sydney, NSW, Australia.
BMC Cancer ; 18(1): 588, 2018 May 24.
Article em En | MEDLINE | ID: mdl-29793444
BACKGROUND: High Dose Rate Brachytherapy (HDRB) boost is a well-established treatment for prostate cancer (PC). We describe the PROstate Multicentre External beam radioTHErapy Using Stereotactic boost (PROMETHEUS) study. Non-surgical stereotactic techniques are used to deliver similar doses to HDRB boost regimens with a dose escalation sub-study. METHODS: Eligible patients have intermediate or high risk PC. PROMETHEUS explores the safety, efficacy and feasibility of multiple Australian centres cooperating in the delivery of Prostate Stereotactic Body Radiotherapy (SBRT) technology. A SBRT boost component Target Dose (TD) of 19Gy in two fractions is to be delivered, followed by a subsequent EBRT component of 46Gy in 23 fractions. Once accrual triggers have been met, SBRT doses can be escalated in 1 Gy increments to a maximum of 22Gy in two fractions. Patient safety will also be measured with the rate of both acute and late moderate to severe Gastro-Intestinal (GI) and Genito-Urinary (GU) Common Terminology Criteria for Adverse Events (CTCAE) toxicities as well as patient reported quality of life. Efficacy will be assessed via biochemical control after 3 years. DISCUSSION: PROMETHEUS aims to generate evidence for a non-surgical possible future alternative to HDRB boost regimens, and introduce advanced radiotherapy techniques across multiple Australian cancer centres. TRIAL REGISTRATION: The study was retrospectively registered on the ANZCTR (Australian New Zealand Clinical Trials Registry) with trial ID: ACTRN12615000223538 .
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Próstata / Lesões por Radiação / Adenocarcinoma / Radiocirurgia / Radioterapia de Intensidade Modulada Tipo de estudo: Clinical_trials / Etiology_studies Aspecto: Patient_preference Limite: Adult / Humans / Male País/Região como assunto: Oceania Idioma: En Revista: BMC Cancer Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Próstata / Lesões por Radiação / Adenocarcinoma / Radiocirurgia / Radioterapia de Intensidade Modulada Tipo de estudo: Clinical_trials / Etiology_studies Aspecto: Patient_preference Limite: Adult / Humans / Male País/Região como assunto: Oceania Idioma: En Revista: BMC Cancer Ano de publicação: 2018 Tipo de documento: Article