Impact of lymph node dissection extent on disease-free survival with postoperative nivolumab plus concurrent chemoradiotherapy in head and neck squamous cell carcinoma: A post-hoc analysis of the NIVOPOSTOP trial.

A Ariane Lapierre (Hospices Civils de Lyon, Pierre Benite, France) A Anne Auperin (Gustave Roussy, Villejuif, France) J Juliette Thariat (Department of Radiation Oncology Baclesse Cancer Center Caen France) C Christian Borel G Gautier Lefebvre (Centre Oscar Lambret, Lille, France) S Severine Racadot (Centre Léon Bérard, Lyon, France) L Lionnel Geoffrois (Institut de Cancérologie de Lorraine, Medical Oncology Department, Vandoeuvre-Lés-Nancy, France) X Xu Shan Sun (Hopital Nord Franche Comté, Montbelliard, France) E Esma Saada J Joanna Kazmierska (Greater Poland Cancer Center, Poznan, Poland) A Amanda Psyrri (Section of Medical Oncology, Department of Internal Medicine, Attikon University Hospital, Faculty of Medicine, National and Kapodistrian University of Athens, School of Medicine, Athens, Greece) R Ricard Mesia (Medical Oncology Department, Catalan Institute of Oncology-Badalona, Germans Trias i Pujol University Hospital, Universitat Autònoma de Barcelona, Badalona-Applied Research Group in Oncology (B-ARGO), Germans Trias I Pujol Research Institute, Badalona, Spain) J Jean Bourhis Y Yungan Tao (Institut Gustave Roussy, Villejuif, France)

Abstract

6001 Background: Postoperative nivolumab added to concurrent Chemo-Radiotherapy (CRT) after surgery has been shown to improve disease-free survival (DFS) in patients with resected head and neck squamous cell carcinoma (HNSCC) at high risk of relapse. However, extensive nodal dissection has long be suspected to hinder response to immunotherapy but prospective data remains scarce. Methods: We analyzed the surgical procedures of the patients included in the primary analysis of the NIVOPOSTOP study regarding neck lymph node dissection (LND). Patients were classified with either uni- or bilateral LND. The number of nodes in the pathological report was also studied. The extent of the LND on DFS was analyzed in univariate and multivariate analysis. Results: Surgical information was available for all 666 patients. Four patients did not undergo any LND. Of the 662 patients who underwent nodal surgery, 239 (36%) underwent unilateral LND and 423 (64%) bilateral LND. The proportion of patients with bilateral / unilateral LND was similar in both treatment. Patients who underwent bilateral LND had statistically higher stage tumors versus unilateral LND (76% vs 61% stage IV) and a significantly higher proportion of laryngeal and hypopharyngeal tumors (17% vs 3% and 16% vs 7% respectively). The median numbers of nodes removed were 39 overall, 25 on the right side of the neck, and 24 on the left. As compared to unilateral LND, bilateral LND was associated with worse DFS in univariate analysis (HR 1.56 (95%CI 1.18; 2.05)). After adjusting for performance status, tumor site and p16 status, clinical stage, pathological risk factors of relapse (nodal extracapsular extension, margin status, perineural invasion, ≥ 4 involved nodes), the association was no longer statistically significant: HR 1.26 (95%CI 0.92; 1.71), Wald test p-value 0.15. There was no interaction between the type of LND (unilateral or bilateral) and the type of treatment (without or with nivolumab) on DFS. The benefit of adding Nivolumab to CRT was similar for unilateral LND (HR 0.79 (95%CI 0.50; 1.26)) and bilateral LND (HR 0.77 (95%CI 0.57; 1.03)) in Cox model stratified for p16 status. Regarding the extent of LND, the benefit of adding Nivolumab to CRT in the 330 patients who underwent removal of more than 39 neck lymph nodes, on one or both sides, was similar to that of the whole population (HR 0.75 (95%CI 0.54; 1.05)). Conclusions: The DFS benefit of adding nivolumab to standard postoperative therapy (cisplatin-RT) was not changed by whether the LND was bilateral or unilateral and persisted in patients in whom more than 39 cervical lymph nodes were removed, on one or both sides. As such, no evidence supports reducing the extent of neck LND when immunotherapy is incorporated into the management of high risk resected HNSCC. Clinical trial information: NCT03576417 .

Article Details

Volume / Issue Vol. 44, Issue 16_suppl
Published June 01, 2026
Pages 6001-6001
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (14)

A

Ariane Lapierre

Hospices Civils de Lyon, Pierre Benite, France

A

Anne Auperin

Gustave Roussy, Villejuif, France

J

Juliette Thariat

Department of Radiation Oncology Baclesse Cancer Center Caen France

C

Christian Borel

G

Gautier Lefebvre

Centre Oscar Lambret, Lille, France

S

Severine Racadot

Centre Léon Bérard, Lyon, France

L

Lionnel Geoffrois

Institut de Cancérologie de Lorraine, Medical Oncology Department, Vandoeuvre-Lés-Nancy, France

X

Xu Shan Sun

Hopital Nord Franche Comté, Montbelliard, France

E

Esma Saada

J

Joanna Kazmierska

Greater Poland Cancer Center, Poznan, Poland

A

Amanda Psyrri

Section of Medical Oncology, Department of Internal Medicine, Attikon University Hospital, Faculty of Medicine, National and Kapodistrian University of Athens, School of Medicine, Athens, Greece

R

Ricard Mesia

Medical Oncology Department, Catalan Institute of Oncology-Badalona, Germans Trias i Pujol University Hospital, Universitat Autònoma de Barcelona, Badalona-Applied Research Group in Oncology (B-ARGO), Germans Trias I Pujol Research Institute, Badalona, Spain

J

Jean Bourhis

Y

Yungan Tao

Institut Gustave Roussy, Villejuif, France