Results from a prospective, randomised study on (accelerated) preoperative versus (conventional) postoperative radiotherapy in treatment of patients with resectable squamous cell carcinoma of the oral cavity - The ARTSCAN 2 study.


Journal

Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology
ISSN: 1879-0887
Titre abrégé: Radiother Oncol
Pays: Ireland
ID NLM: 8407192

Informations de publication

Date de publication:
01 2022
Historique:
received: 20 07 2021
revised: 03 11 2021
accepted: 07 11 2021
pubmed: 19 11 2021
medline: 20 4 2022
entrez: 18 11 2021
Statut: ppublish

Résumé

An earlier prospective randomised multicentre study (ARTSCAN) in head and neck cancer patients that compared conventionally fractionated radiotherapy (CF) with accelerated radiotherapy (AF) was inconclusive. In the subgroup of oral cavity squamous cell cancer (OCSCC) a large absolute, but not statistically significant, difference in local control was seen in favour of AF. This difference was more pronounced in resectable tumours. The finding raised the hypothesis that AF could be beneficial for OCSCC patients. In addition, the longstanding controversy on pre- or postoperative radiotherapy was addressed. Patients with OCSCC, judged to withstand and likely benefit from combined therapy, were recruited. Subjects were randomised to either preoperative AF with 43 fractions given as a concomitant boost with two fractions/day to the tumour bearing volume to a total dose of 68 Gy in 4.5 weeks followed by surgery, or primary surgery with postoperative CF, total dose 60 or 66 Gy in 6-7 weeks. For patients whose tumours had high-risk features, 66 Gy and concomitant cisplatin was prescribed. 250 patients were randomised. Median follow-up was 5 years for locoregional control (LRC) and 9 years for overall survival (OS). There were no statistically significant differences between the two treatment arms regarding LRC and OS. LRC at five years was 73% (95% CI, 65-82) in preoperative AF and 78% (95% CI, 70-85) in postoperative CF. Toxicity was more pronounced in preoperative AF. This study does not support that AF prior to surgery improves outcome in oral cavity cancer compared with postoperative CF.

Sections du résumé

BACKGROUND AND PURPOSE
An earlier prospective randomised multicentre study (ARTSCAN) in head and neck cancer patients that compared conventionally fractionated radiotherapy (CF) with accelerated radiotherapy (AF) was inconclusive. In the subgroup of oral cavity squamous cell cancer (OCSCC) a large absolute, but not statistically significant, difference in local control was seen in favour of AF. This difference was more pronounced in resectable tumours. The finding raised the hypothesis that AF could be beneficial for OCSCC patients. In addition, the longstanding controversy on pre- or postoperative radiotherapy was addressed.
MATERIALS AND METHODS
Patients with OCSCC, judged to withstand and likely benefit from combined therapy, were recruited. Subjects were randomised to either preoperative AF with 43 fractions given as a concomitant boost with two fractions/day to the tumour bearing volume to a total dose of 68 Gy in 4.5 weeks followed by surgery, or primary surgery with postoperative CF, total dose 60 or 66 Gy in 6-7 weeks. For patients whose tumours had high-risk features, 66 Gy and concomitant cisplatin was prescribed.
RESULTS
250 patients were randomised. Median follow-up was 5 years for locoregional control (LRC) and 9 years for overall survival (OS). There were no statistically significant differences between the two treatment arms regarding LRC and OS. LRC at five years was 73% (95% CI, 65-82) in preoperative AF and 78% (95% CI, 70-85) in postoperative CF. Toxicity was more pronounced in preoperative AF.
CONCLUSION
This study does not support that AF prior to surgery improves outcome in oral cavity cancer compared with postoperative CF.

Identifiants

pubmed: 34793864
pii: S0167-8140(21)08996-9
doi: 10.1016/j.radonc.2021.11.008
pii:
doi:

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

26-32

Investigateurs

Anders Högmo (A)
Lalle Hammarstedt-Nordenvall (L)
Helena Sjödin (H)
Gun Wickart-Johansson (G)
Lovisa Farnebo (L)
Jan Rzpecki (J)
Britta Lödén (B)
Lena Cederblad (L)
Tomas Ekberg (T)
Stefan Bergström (S)

Informations de copyright

Copyright © 2021 The Authors. Published by Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Conflict of interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Johan Wennerberg (J)

Department of ORL, Head & Neck Surgery, Skåne University Hospital, Lund University, Sweden.

Maria Gebre-Medhin (M)

Department of Hematology, Oncology and Radiation Physics, Skåne University Hospital, Lund University, Sweden.

Per Nilsson (P)

Department of Hematology, Oncology and Radiation Physics, Skåne University Hospital, Lund University, Sweden.

Eva Brun (E)

Department of Hematology, Oncology and Radiation Physics, Skåne University Hospital, Lund University, Sweden.

Elisabeth Kjellén (E)

Department of Hematology, Oncology and Radiation Physics, Skåne University Hospital, Lund University, Sweden.

Kristin Carlwig (K)

Department of ORL, Head & Neck Surgery, Skåne University Hospital, Lund University, Sweden.

Johan Reizenstein (J)

Department of Oncology, Örebro University Hospital, Sweden.

Stefan Kristiansson (S)

Department of Otolaryngology, Örebro University Hospital, Sweden.

Karin Söderkvist (K)

Department of Radiation Sciences, Oncology, Umeå University, Sweden.

Magnus Wahlgren (M)

Department of Clinical Sciences, Otolaryngology Umeå University, Sweden.

Björn Zackrisson (B)

Department of Radiation Sciences, Oncology, Umeå University, Sweden. Electronic address: bjorn.zackrisson@umu.se.

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