Equivalence Randomized Trial to Compare Treatment on the Basis of Sentinel Node Biopsy Versus Neck Node Dissection in Operable T1-T2N0 Oral and Oropharyngeal Cancer

Author:

Garrel Renaud1ORCID,Poissonnet Gilles2,Moyà Plana Antoine3,Fakhry Nicolas4ORCID,Dolivet Gilles5,Lallemant Benjamin6,Sarini Jérôme7ORCID,Vergez Sebastien7,Guelfucci Bruno8,Choussy Olivier9ORCID,Bastit Vianney10ORCID,Richard Fanny1,Costes Valérie11,Landais Paul12,Perriard Françoise12,Daures Jean Pierre12,de Verbizier Delphine13,Favier Valentin1ORCID,de Boutray Marie1ORCID

Affiliation:

1. Head Neck Surgery Department, Montpellier University Hospital Center, Montpellier, France

2. Head Neck Surgery Department, Antoine Lacassagne Center, Nice, France

3. Head Neck Surgery Department, Institut Gustave Roussy, Villejuif, France

4. Head Neck Surgery Department, Marseille University Hospital Center, Marseille, France

5. Head Neck Surgery Department, Alexis Vautrin Center, Vandœuvre-lès-Nancy, France

6. Head Neck Surgery Department, Nîmes University Hospital Center, Nîmes, France

7. Head Neck Surgery Department, Toulouse Oncopole, Toulouse, France

8. Head Neck Surgery Department, Toulon Hospital Center, Toulon, France

9. Head Neck Surgery Department, Curie Institute, Paris, France

10. Head Neck Surgery Department, François Baclesse Center, Caen, France

11. Pathology Department, Montpellier University Hospital Center, Montpellier, France

12. Clinical Research University Institute, UPRES EA 2415, Montpellier, France

13. Nuclear Medicine Department, Montpellier University Hospital Center, Montpellier, France

Abstract

PURPOSE Sentinel node (SN) biopsy is accurate in operable oral and oropharyngeal cT1-T2N0 cancer (OC), but, to our knowledge, the oncologic equivalence of SN biopsy and neck lymph node dissection (ND; standard treatment) has never been evaluated. METHODS In this phase III multicenter trial, 307 patients with OC were randomly assigned to (1) the ND arm or (2) the SN arm (experimental arm: biopsy alone if negative, or followed by ND if positive, during primary tumor surgery). The primary outcome was neck node recurrence-free survival (RFS) at 2 years. Secondary outcomes were 5-year neck node RFS, 2- and 5-year disease-specific survival (DSS), and overall survival (OS). Other outcomes were hospital stay length, neck and shoulder morbidity, and number of physiotherapy prescriptions during the 2 years after surgery. RESULTS Data on 279 patients (139 ND and 140 SN) could be analyzed. Neck node RFS was 89.6% (95% CI, 0.83% to 0.94%) at 2 years in the ND arm and 90.7% (95% CI, 0.84% to 0.95%) in the SN arm, confirming the equivalence with P < .01. The 5-year RFS and the 2- and 5-year DSS and OS were not significantly different between arms. The median hospital stay length was 8 days in the ND arm and 7 days in the SN arm ( P < .01). The functional outcomes were significantly worse in the ND arm until 6 months after surgery. CONCLUSION This study demonstrated the oncologic equivalence of the SN and ND approaches, with lower morbidity in the SN arm during the first 6 months after surgery, thus establishing SN as the standard of care in OC.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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