A phase III randomized controlled trial comparing palliative stereotactic body radiotherapy vs. palliative standard radiotherapy in patients with advanced head and neck cancer (NCT06641791).

I Ian Poon (Sunnybrook Health Sciences Centre, Toronto, ON, Canada) I Irene Karam (Sunnybrook Health Sciencies, Toronto, ON, Canada) H Houda Bahig (Centre Hospitalier de l'Université de Montréal, Montreal, QC, Canada) B Brock J. Debenham (Cross Cancer Institute, University of Alberta, Edmonton, AB, Canada) A Adam Mutsaers (London Health Sciences Centre, Western University, London, ON, Canada) M Murali M. Rajaraman (QEII HSC - Nova Scotia Cancer Center, Halifax, NS, Canada) C Chiaojung Jillian Tsai (Princess Margaret Hospital, University Health Network, Toronto, ON, Canada) L Lee Chin M Madette Galapin (Department of Radiation Therapy, Sunnybrook Health Sciences Centre, Toronto, ON, Canada) S Scott Victor Bratman (Princess Margaret Cancer Centre, University Health Network; Department of Medical Biophysics, University of Toronto; Adela, Inc., Toronto, ON, Canada) J Jolie Ringash (Princess Margaret - University Health Network, Toronto, ON, Canada) A Ambika Parmar (Sunnybrook Health Sciences Centre, Odette Cancer Centre, University of Toronto, Toronto, ON, Canada) K Koren S. Smith (University of Massachusetts Chan Medical School, Worcester, MA) S Sarah Radcliffe (Canadian Cancer Trials Group, Kingston, ON, Canada) W Wei Tu (State Key Laboratory of Metastable Materials Science and Technology) W Wendy R. Parulekar (Canadian Cancer Trials Group, Kingston, ON, Canada)

Abstract

TPS6118 Background: The optimal radiotherapy (RT) treatment regimen for patients with advanced head and neck cancer (AHNC) unsuitable to receive curative intent RT is undefined. Stereotactic body radiotherapy (SBRT) is a promising technique but rigorous multicentre evaluation is required prior to adoption. Methods: This is a Phase III randomized controlled trial comparing palliative SBRT to palliative standard RT (SRT) in participants with advanced mucosal, squamous cell head and neck cancer unable to tolerate curative intent RT. Key eligibility criteria: Unsuitable for curative intent therapy, no evidence of metastatic disease, stages TX or T0-T4/N0-N3, geriatric 8 score [1] ≤14. Treatment arms: (Experimental) SBRT 4500 cGy/ 5fr (twice a week to primary and nodal GTV (BED 10 85) OR 4000 cGy /5 fr twice a week if organs at risk (BED 10 -72) versus (standard) 2400 cGy/ 3fr (day 0/7/21 (BED 10 43) or 2500 cGy/ 5fr over 1 week (BED 10 38). Primary objective: To compare OS between arms. Secondary objectives evaluate progression-free survival (PFS), locoregional failure-free survival, distant metastases-free survival, response rates, acute and long-term toxicity (CTCAE v5.0), treatment compliance, patient-reported outcomes (PRO-CTCAE, FACT-HN), resource utilization, and health utilities. Statistical design : The trial aims to enroll 196 patients with a 2:1 randomization ratio (SBRT:SRT). The study is powered at 80% with a two-sided alpha of 0.05 to detect a difference in 1-year OS of 40.3% vs. 22% (HR = 0.6), assuming a 15% drop-out/lost to follow-up rate. Conduct to Date : This trial was activated on October 31, 2024. Supported by CCS grant #707213; CIHR #175014. [1] Takahashi M, Takahashi M, Komine K, Yamada H, Kasahara Y, Chikamatsu S, et al. (2017) The G8 screening tool enhances prognostic value to ECOG performance status in elderly cancer patients: A retrospective, single institutional study. PLoS ONE 12(6): e0179694. https://doi.org/10.1371/journal.pone.0179694. Clinical trial information: NCT06641791 .

Article Details

Volume / Issue Vol. 43, Issue 16_suppl
Published June 01, 2025
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (16)

I

Ian Poon

Sunnybrook Health Sciences Centre, Toronto, ON, Canada

I

Irene Karam

Sunnybrook Health Sciencies, Toronto, ON, Canada

H

Houda Bahig

Centre Hospitalier de l'Université de Montréal, Montreal, QC, Canada

B

Brock J. Debenham

Cross Cancer Institute, University of Alberta, Edmonton, AB, Canada

A

Adam Mutsaers

London Health Sciences Centre, Western University, London, ON, Canada

M

Murali M. Rajaraman

QEII HSC - Nova Scotia Cancer Center, Halifax, NS, Canada

C

Chiaojung Jillian Tsai

Princess Margaret Hospital, University Health Network, Toronto, ON, Canada

L

Lee Chin

M

Madette Galapin

Department of Radiation Therapy, Sunnybrook Health Sciences Centre, Toronto, ON, Canada

S

Scott Victor Bratman

Princess Margaret Cancer Centre, University Health Network; Department of Medical Biophysics, University of Toronto; Adela, Inc., Toronto, ON, Canada

J

Jolie Ringash

Princess Margaret - University Health Network, Toronto, ON, Canada

A

Ambika Parmar

Sunnybrook Health Sciences Centre, Odette Cancer Centre, University of Toronto, Toronto, ON, Canada

K

Koren S. Smith

University of Massachusetts Chan Medical School, Worcester, MA

S

Sarah Radcliffe

Canadian Cancer Trials Group, Kingston, ON, Canada

W

Wei Tu

State Key Laboratory of Metastable Materials Science and Technology

W

Wendy R. Parulekar

Canadian Cancer Trials Group, Kingston, ON, Canada