Clinical Outcomes of a Randomized Trial of Adaptive Plan-of-the-Day Treatment in Patients Receiving Ultra-hypofractionated Weekly Radiation Therapy for Bladder Cancer.


Journal

International journal of radiation oncology, biology, physics
ISSN: 1879-355X
Titre abrégé: Int J Radiat Oncol Biol Phys
Pays: United States
ID NLM: 7603616

Informations de publication

Date de publication:
01 06 2021
Historique:
received: 28 08 2020
revised: 18 11 2020
accepted: 25 11 2020
pubmed: 15 12 2020
medline: 27 8 2021
entrez: 14 12 2020
Statut: ppublish

Résumé

Hypofractionated radiation therapy can be used to treat patients with muscle-invasive bladder cancer unable to have radical therapy. Toxicity is a key concern, but adaptive plan-of the day (POD) image-guided radiation therapy delivery could improve outcomes by minimizing the volume of normal tissue irradiated. The HYBRID trial assessed the multicenter implementation, safety, and efficacy of this strategy. HYBRID is a Phase II randomized trial that was conducted at 14 UK hospitals. Patients with T2-T4aN0M0 muscle-invasive bladder cancer unsuitable for radical therapy received 36 Gy in 6 weekly fractions, randomized (1:1) to standard planning (SP) or adaptive planning (AP) using a minimization algorithm. For AP, a pretreatment cone beam computed tomography (CT) was used to select the POD from 3 plans (small, medium, and large). Follow-up included standard cystoscopic, radiologic, and clinical assessments. The primary endpoint was nongenitourinary Common Terminology Criteria for Adverse Events (CTCAE) grade ≥ 3 (≥G3) toxicity within 3 months of radiation therapy. A noncomparative single stage design aimed to exclude ≥30% toxicity rate in each planning group in patients who received ≥1 fraction of radiation therapy. Local control at 3-months (both groups combined) was a key secondary endpoint. Between April 15, 2014, and August 10, 2016, 65 patients were enrolled (SP, n = 32; AP, n = 33). The median follow-up time was 38.8 months (interquartile range [IQR], 36.8-51.3). The median age was 85 years (IQR, 81-89); 68% of participants (44 of 65) were male; and 98% of participants had grade 3 urothelial cancer. In 63 evaluable participants, CTCAE ≥G3 nongenitourinary toxicity rates were 6% (2 of 33; 95% confidence interval [CI], 0.7%-20.2%) for the AP group and 13% (4 of 30; 95% CI, 3.8%-30.7%) for the SP group. Disease was present in 9/48 participants assessed at 3 months, giving a local control rate of 81.3% (95% CI, 67.4%-91.1%). POD adaptive radiation therapy was successfully implemented across multiple centers. Weekly ultrahypofractionated 36 Gy/6 fraction radiation therapy is safe and provides good local control rates in this older patient population.

Identifiants

pubmed: 33316362
pii: S0360-3016(20)34640-X
doi: 10.1016/j.ijrobp.2020.11.068
pmc: PMC8114997
pii:
doi:

Types de publication

Clinical Trial, Phase II Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

412-424

Subventions

Organisme : Department of Health
Pays : United Kingdom
Organisme : Cancer Research UK
ID : C8262/A14744
Pays : United Kingdom
Organisme : Cancer Research UK
ID : CRUK/12/055
Pays : United Kingdom
Organisme : Cancer Research UK
ID : C1491/A15955
Pays : United Kingdom
Organisme : Cancer Research UK
ID : C1491/A25351
Pays : United Kingdom

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2020 The Authors. Published by Elsevier Inc. All rights reserved.

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Auteurs

Robert Huddart (R)

The Institute of Cancer Research, London, United Kingdom; Royal Marsden NHS Foundation Trust, London, United Kingdom. Electronic address: Robert.Huddart@icr.ac.uk.

Shaista Hafeez (S)

The Institute of Cancer Research, London, United Kingdom; Royal Marsden NHS Foundation Trust, London, United Kingdom.

Rebecca Lewis (R)

The Institute of Cancer Research, London, United Kingdom.

Helen McNair (H)

Royal Marsden NHS Foundation Trust, London, United Kingdom.

Isabelle Syndikus (I)

Radiotherapy Department, Oxford University Hospitals NHS Foundation Trust, Oxford, United Kingdom.

Ann Henry (A)

Leeds Teaching Hospitals NHS Trust, Leeds, United Kingdom.

John Staffurth (J)

Velindre University NHS Trust, Cardiff, United Kingdom.

Monisha Dewan (M)

The Institute of Cancer Research, London, United Kingdom.

Catalina Vassallo-Bonner (C)

Patient representative, Institute of Cancer Research, London, United Kingdom.

Syed Ali Moinuddin (SA)

Academic unit of Oncology, Department of Oncology and Metabolism, Medical School, University of Sheffield, Sheffield, United Kingdom.

Alison Birtle (A)

Lancashire Teaching Hospitals NHS Foundation Trust, Preston, United Kingdom.

Gail Horan (G)

Queen Elizabeth Hospital Kings Lynn NHS Trust, Kings Lynn, United Kingdom.

Yvonne Rimmer (Y)

Cambridge University Hospitals NHS Foundation Trust, Cambridge, United Kingdom.

Ramachandran Venkitaraman (R)

East Suffolk and North Essex NHS Foundation Trust, Ipswich, United Kingdom.

Vincent Khoo (V)

Royal Marsden NHS Foundation Trust, London, United Kingdom.

Anita Mitra (A)

University College London Hospitals NHS Foundation Trust, London, United Kingdom.

Simon Hughes (S)

Guy's and St Thomas' NHS Foundation Trust, London, United Kingdom.

Stephanie Gibbs (S)

Barking, Havering and Redbridge University Hospitals NHS Trust, Romford, United Kingdom.

Gaurav Kapur (G)

Norfolk and Norwich University Hospitals NHS Foundation Trust, Norwich, United Kingdom.

Angela Baker (A)

Radiotherapy Department, Oxford University Hospitals NHS Foundation Trust, Oxford, United Kingdom.

Vibeke Nordmark Hansen (VN)

Odense University Hospital, Odense, Denmark.

Emma Patel (E)

Radiotherapy Trials Quality Assurance Group, Mount Vernon Cancer Centre, Northwood, United Kingdom.

Emma Hall (E)

The Institute of Cancer Research, London, United Kingdom.

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Classifications MeSH