Locoregional control, progression-free survival and morbidity rates in N3 head and neck cancer patients with low primary tumour burden: A 301-patient study.


Journal

Clinical otolaryngology : official journal of ENT-UK ; official journal of Netherlands Society for Oto-Rhino-Laryngology & Cervico-Facial Surgery
ISSN: 1749-4486
Titre abrégé: Clin Otolaryngol
Pays: England
ID NLM: 101247023

Informations de publication

Date de publication:
Nov 2020
Historique:
received: 14 01 2020
revised: 26 05 2020
accepted: 21 07 2020
pubmed: 31 7 2020
medline: 23 11 2021
entrez: 31 7 2020
Statut: ppublish

Résumé

In patients with N3 head and neck squamous cell carcinoma (HNSCC), N3 disease is associated with high regional relapse and metastatic risks. Patients with resectable N3 disease have better prognosis although their metastatic risk may be similar as in patients with unresectable disease. Neoadjuvant chemotherapy has been associated with lower metastatic rates, but N3 patients may die of rapid locoregional progression. We assessed outcomes with the three modalities in patients with low primary burden to better assess the specific prognosis of N3 disease. This retrospective multicentric study included T0-2 N3 HNSCC patients. Outcomes and morbidity in upfront neck dissection (uND) vs non-surgical groups were analysed and oncological outcomes and morbidity compared between patients undergoing chemoradiation or neoadjuvant chemotherapy in patients with initially unresectable N3 nodes. Of 301 patients, 142 (47%) underwent uND, 68 (23%) neoadjuvant chemotherapy and 91 (30%) chemoradiation. The 24- and 60-month incidence of locoregional relapse was 23.2% [18.3%; 28.4%] and 27.4% [21.8%; 33.3%]; it was lower in patients undergoing uND (P = .006). In patients with non-surgical treatments, success rates were 57.8% [49.4%; 66.3%] after chemoradiation and 38.1% [29.6%; 46.7%] after neoadjuvant chemotherapy (P = .001). Overall morbidity was more frequent in patients undergoing uND (68.8%) (P < .001). uND improved locoregional control but increased morbidity and showed no survival benefit. Success rates were better after chemoradiation versus neoadjuvant chemotherapy. Neoadjuvant chemotherapy did not reduce metastatic rates but non-responders to chemoradiation had poor PFS and survival rate, suggesting that predictive criteria are warranted.

Identifiants

pubmed: 32729227
doi: 10.1111/coa.13615
doi:

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

877-884

Informations de copyright

© 2020 John Wiley & Sons Ltd.

Références

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Auteurs

Florent Carsuzaa (F)

Head and neck surgery, University Hospital of Poitiers, Poitiers, France.

Xavier Dufour (X)

Head and neck surgery, University Hospital of Poitiers, Poitiers, France.

Philippe Gorphe (P)

Department of Head and Neck Oncology, Gustave Roussy, University Paris-Saclay, Villejuif, France.

Christian Righini (C)

Head and neck surgery, University Hospital of Grenoble, Grenoble, France.

Alain Cosmidis (A)

Head and neck surgery, University Hospital of Lyon, Lyon, France.

Maximilien Rogé (M)

Radiation oncology, Centre Henri Becquerel, Rouen, France.

Erwan De Mones (E)

Head and neck surgery, University Hospital of Bordeaux, Bordeaux, France.

Stéphanie Servagi Vernat (S)

Radiation oncology, Centre Jean Godinot, Reims, France.

Denis Tonnerre (D)

Head and neck surgery, University Hospital of Poitiers, Poitiers, France.

Sylvain Morinière (S)

Head and neck surgery, University Hospital of Tours, Tours, France.

Amaury Dugas (A)

Head and neck surgery, University Hospital of Caen, Caen, France.

Olivier Malard (O)

Head and neck surgery, University Hospital of Nantes, Nantes, France.

François Pasquier (F)

Head and neck surgery, University Hospital of Nantes, Nantes, France.

Sébastien Vergez (S)

Head and neck surgery, Institut Universitaire du Cancer de Toulouse Oncopole / University Hospital of Toulouse, Toulouse, France.

Ulrike Schick (U)

Radiation oncology, University Hospital of Brest, Brest, France.

Michael Gérard (M)

Radiation oncology, Centre François Baclesse / ARCHADE, Caen, France.

Julia Salleron (J)

Cellule Data Biostatistique, Institut de Cancérologie de Lorraine, Université de Lorraine, Vandœuvre-lès-Nancy, France.

Juliette Thariat (J)

Radiation oncology, Centre François Baclesse / ARCHADE, Caen, France.

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