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TROG 15.03 phase II clinical trial of Focal Ablative STereotactic Radiosurgery for Cancers of the Kidney

Authors :
Tomas Kron
Eddie Lau
Nathan Lawrentschuk
Jeremy D Ruben
Swetha Sridharan
Ben G. L. Vanneste
Shankar Siva
Michael S Hofman
Nicholas Hardcastle
Mathias Bressel
Brent Chesson
Nicholas R. Brook
Jarad Martin
Farshad Foroudi
David Pryor
Vincent Khoo
Hayley M. Reynolds
Rebecca Montgomery
Braden Higgs
Richard De Abreu Lourenco
Radiotherapie
RS: GROW - R3 - Innovative Cancer Diagnostics & Therapy
Source :
BMC Cancer, 18:1030, 1-10. BioMed Central Ltd, BMC Cancer, Vol 18, Iss 1, Pp 1-10 (2018), BMC Cancer
Publication Year :
2018
Publisher :
BioMed Central Ltd, 2018.

Abstract

Stereotactic ablative body radiotherapy (SABR) is a non-invasive alternative to surgery to control primary renal cell cancer (RCC) in patients that are medically inoperable or at high-risk of post-surgical dialysis. The objective of the FASTRACK II clinical trial is to investigate the efficacy of SABR for primary RCC. FASTRACK II is a single arm, multi-institutional phase II study. Seventy patients will be recruited over 3 years and followed for a total of 5 years. Eligible patients must have a biopsy confirmed diagnosis of primary RCC with a single lesion within a kidney, have ECOG performance ≤2 and be medically inoperable, high risk or decline surgery. Radiotherapy treatment planning is undertaken using four dimensional CT scanning to incorporate the impact of respiratory motion. Treatment must be delivered using a conformal or intensity modulated technique including IMRT, VMAT, Cyberknife or Tomotherapy. The trial includes two alternate fractionation schedules based on tumour size: for tumours ≤4 cm in maximum diameter a single fraction of 26Gy is delivered; and for tumours > 4 cm in maximum diameter 42Gy in three fractions is delivered. The primary outcome of the study is to estimate the efficacy of SABR for primary RCC. Secondary objectives include estimating tolerability, characterising overall survival and cancer specific survival, estimating the distant failure rate, describing toxicity and renal function changes after SABR, and assessment of cost-effectiveness of SABR compared with current therapies. The present study design allows for multicentre prospective validation of the efficacy of SABR for primary RCC that has been observed from prior single institutional and retrospective series. The study also allows assessment of treatment related toxicity, overall survival, cancer specific survival, freedom from distant failure and renal function post therapy. Clinicaltrials.gov NCT02613819 , registered Nov 25th 2015.

Details

Language :
English
ISSN :
14712407
Volume :
18
Database :
OpenAIRE
Journal :
BMC Cancer
Accession number :
edsair.doi.dedup.....000e4623ba2b0e8bbfc3926e417aab46