Randomized Trial of Radiation Therapy With Weekly Cisplatin or Cetuximab in Low-Risk HPV-Associated Oropharyngeal Cancer (TROG 12.01) - A Trans-Tasman Radiation Oncology Group Study.


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:
15 11 2021
Historique:
received: 18 02 2021
revised: 05 04 2021
accepted: 12 04 2021
pubmed: 8 6 2021
medline: 19 2 2022
entrez: 7 6 2021
Statut: ppublish

Résumé

The excellent prognosis of patients with low-risk human papillomavirus (HPV)- associated oropharyngeal squamous cell carcinoma has led to concerns about overtreatment and excessive toxicity with radiation therapy and cisplatin, leading to interest in de-intensification trials. We investigated whether cetuximab, an epidermal growth factor receptor targeting antibody, when combined with radiation therapy would result in a decrease in symptom burden and toxicity with similar efficacy compared with weekly cisplatin. TROG12.01, a randomized, multicenter trial involving 15 sites in Australia and New Zealand enrolled patients with HPV-associated oropharyngeal squamous cell carcinoma, American Joint Committee on Cancer 7th edition stage III (excluding T1-2N1) or stage IV (excluding T4 and/or N3 and/or N2b-c if smoking history >10 pack years and/or distant metastases). Patients were randomized (1:1) to receive radiation therapy (70 Gy in 35 fractions) with either weekly cisplatin, 7 doses of 40 mg/m Between June 17, 2013, and June 7, 2018, 189 patients were enrolled, with 92 in cisplatin arm and 90 in cetuximab included in the main analysis. There was no difference in the primary endpoint of symptom severity; difference in area under the curve cetuximab-cisplatin was 0.05 (95% confidence interval [CI], -0.19, 0.30), P = .66. The T-score (mean number of ≥grade 3 acute adverse events) was 4.35 (standard deviation 2.48) in the cisplatin arm and 3.82 (standard deviation 1.8) in the cetuximab arm, P = .108. The 3-year failure-free survival rates were 93% (95% CI, 86%-97%) in the cisplatin arm and 80% (95% CI, 70%-87%) in the cetuximab arm (hazard ratio = 3.0 [95% CI, 1.2-7.7]); P = .015. For patients with low-risk HPV-associated oropharyngeal cancer, radiation therapy and cetuximab had inferior failure-free survival without improvement in symptom burden or toxicity compared with radiation therapy and weekly cisplatin. Radiation therapy and cisplatin remain the standard of care.

Identifiants

pubmed: 34098030
pii: S0360-3016(21)00376-X
doi: 10.1016/j.ijrobp.2021.04.015
pii:
doi:

Substances chimiques

Cetuximab PQX0D8J21J
Cisplatin Q20Q21Q62J

Banques de données

ClinicalTrials.gov
['NCT01855451']

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

876-886

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2021 Elsevier Inc. All rights reserved.

Auteurs

Danny Rischin (D)

Department of Medical Oncology, Peter MacCallum Cancer Centre, Melbourne, Australia; Sir Peter MacCallum Department of Oncology, University of Melbourne, Melbourne, Australia. Electronic address: danny.rischin@petermac.org.

Madeleine King (M)

University of Sydney, School of Psychology, Sydney Quality of Life Office, Sydney, Australia.

Lizbeth Kenny (L)

Department of Radiation Oncology, Royal Brisbane & Women's Hospital, Brisbane, Australia; Faculty of Medicine, University of Queensland, Brisbane, Australia.

Sandro Porceddu (S)

Faculty of Medicine, University of Queensland, Brisbane, Australia; Department of Radiation Oncology, Princess Alexandra Hospital, Brisbane, Australia.

Christopher Wratten (C)

Department of Radiation Oncology, Calvary Mater Hospital and University of Newcastle, Newcastle, Australia.

Andrew Macann (A)

Department of Radiation Oncology, Auckland City Hospital and University of Auckland, Auckland, New Zealand.

James E Jackson (JE)

Icon Cancer Centres, Gold Coast, Australia.

Mathias Bressel (M)

Centre for Biostatistics and Clinical Trials, Peter MacCallum Cancer Centre, Melbourne, Australia.

Alan Herschtal (A)

Centre for Biostatistics and Clinical Trials, Peter MacCallum Cancer Centre, Melbourne, Australia.

Richard Fisher (R)

Centre for Biostatistics and Clinical Trials, Peter MacCallum Cancer Centre, Melbourne, Australia.

Tsien Fua (T)

Division of Radiation Oncology, Peter MacCallum Cancer Centre, Melbourne, Australia.

Charles Lin (C)

Department of Radiation Oncology, Royal Brisbane & Women's Hospital, Brisbane, Australia.

Chen Liu (C)

Division of Radiation Oncology, Peter MacCallum Cancer Centre, Melbourne, Australia.

Brett G M Hughes (BGM)

Faculty of Medicine, University of Queensland, Brisbane, Australia; Department of Medical Oncology, Royal Brisbane & Women's Hospital, Brisbane, Australia.

Margaret McGrath (M)

Department of Medical Oncology, Princess Alexandra Hospital, Brisbane, Australia.

Lachlan McDowell (L)

Sir Peter MacCallum Department of Oncology, University of Melbourne, Melbourne, Australia; Division of Radiation Oncology, Peter MacCallum Cancer Centre, Melbourne, Australia.

June Corry (J)

Genesiscare St Vincent's Hospital, Melbourne, Australia; Department of Medicine, University of Melbourne, Melbourne, Australia.

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Classifications MeSH