Clinical trial · Interventional
Randomized, Open-label Economic and Medical Study on the Lymph Node Management of Squamous Cell Carcinoma of the Oral Cavity and Oropharynx Tumor Stage 1 or 2, Nodes 0 (T1-T2 N0) Operable
Randomized, Open-label Economic and Medical Study on the Lymph Node Management of Squamous Cell Carcinoma of the Oral Cavity and Oropharynx T1-T2N0 Operable : Comparison of the Reference Strategy Based on a the Systematic Lymph Node Dissection Versus the Strategy Based on the Technique of Sentinel Lymph Node.
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
Currently, patients with cancer of oral cavity or oropharynx T1-T2N0 classified, are treated surgically with systematic lymph node dissection while in 70%, there is no lymph node metastasis. The technique of identifying the sentinel node (GS) is validated for these tumors because the status of the sentinel node is predictive of the other nodes status in the neck. This helps to diagnose the presence of metastases without lymph node dissection and thus select patients requiring a treatment node. However, the oncological and functional results of a therapeutic strategy based on identifying the GS is unknown. This open-label randomized multicenter clinical trial aims to compare the oncologic and functional outcome of two strategies : the current management versus the management based on the sentinel lymph node. The hypothesis is based on a nodal control difference at 2 years in both arms not exceeding 10%. The medico-economic analysis will be conducted in two stages : a classic stage on 2 years with estimated incremental cost-effectiveness and incremental cost-utility, then a step with log term modeling. A reduction in morbidity and treatment costs in the sentinel node arm are expected in this study.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Head and Neck Tumors | Head and Neck Neoplasm | ALIAS | 0.90 |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Surgery: Classic strategy | Other | — | UNRESOLVED |
| Surgery: GS strategy | Other | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- ACTIVE_COMPARATOR
- label
- GS strategy
- description
- sentinel node biopsy
- interventionNames
- Other: Surgery: GS strategy
- type
- OTHER
- label
- Classic strategy
- description
- systematic lymphadenectomy
- interventionNames
- Other: Surgery: Classic strategy
Primary outcomes (1)
- measure
- Nodal recurrence rate
- timeFrame
- 24 months after the surgery
- description
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion criteria: 1. Man or woman age over 18 without upper age limit 2. Social Insured 3. Patient Information and Informed Consent signed by the patient 4. Patient not participating in another trial since the legal time 5. Absence of any previous treatment for cancer of the Upper AeroDigestive Tract (VADS) 6. Patient with primary squamous cell carcinoma of the oral cavity or oropharynx documented by biopsy with histopathologic analysis not older than 1 month 7. curable or operable tumor with radiation under the Tumor, Nodes, Metastasis (TNM) stage, location and the patient's general condition 8. Stage T1 and T2 9. Tumor listed N0 satisfying the following conditions (21 days validity period): A) absence of lymphadenopathy palpable on clinical examination of the ENT investigator. B) CT scan or MRI with injection of contrast product: lack of suspicious adenomegaly for metastasis = node size less than one centimeter and 1.5 cm for the group IIa, ovoid, homogeneous, not taking contrast and showing no signs of lymph perinodal invasion ( hyperdensity fat, vascular adhesion), absence of lymph node group (\> 3) 10. Systematic ENT endoscopy eliminating a second synchronous tumor and precisely establishing the T (21 days validity period) 11. Absence of metastasis: M0 Exclusion criteria: 1. Failure of one of the inclusion criteria 2. Other cancer being treated 3. Non-invasive tumor: high-grade dysplasia, carcinoma in situ 4. Inadequate tumor excision: margins invaded without further recovery in safe zone 5. Contraindications to surgery such sentinel node or lymph node dissection 6. Contraindications to radiotherapy 7. Contraindications to performing a scan: * Known allergy or intolerance to the injected product and particularly with Technetium-99 * Pregnancy 8. Refusal to accept the full treatment regardless of the strategy 9. Follow-up not possible 10. Refusal to accept the described follow-up and / or provide the necessary information for the study 11. Patient already treated for the tumor outside an excision biopsy 12. Patient who previously had chemotherapy or immunotherapy for another cancer outside VADS within less than 6 months 13. Patient undergoing cervical or VADS radiotherapy whatever the cause or time 14. Patient who have had cervical spine surgery regardless of the cause or time
References
Publications (1)
- DERIVEDGarrel R, Poissonnet G, Moya Plana A, Fakhry N, Dolivet G, Lallemant B, Sarini J, Vergez S, Guelfucci B, Choussy O, Bastit V, Richard F, Costes V, Landais P, Perriard F, Daures JP, de Verbizier D, Favier V, de Boutray M. 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. J Clin Oncol. 2020 Dec 1;38(34):4010-4018. doi: 10.1200/JCO.20.01661. Epub 2020 Oct 14. PMID 33052754