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NCT Number: NCT05774483

Sentinel Node Biopsy Versus Limited Elective Neck Dissection in Early Cancers of Oral Cavity NoDe Negative

The goal of this clinical trial is to compare the survival outcomes, morbidity and cost-effectiveness of sentinel node biopsy versus limited elective neck dissection in node-negative early oral cancers.

The main questions it aims to answer are:

* Survival outcomes * Morbidity outcomes * Cost-effectiveness

Participants will either undergo sentinel node biopsy followed by completion neck dissection if sentinel node is reported to be metastatic (SNB) or limited elective neck dissection where level IIb will be cleared only if level IIa is metastatic (limited END). The study will compare the outcomes in the two cohorts.

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Key information

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Tata Memorial Hospital, Mumbai, Maharashtra, India

Loading trial locations.

About this study

Based on the current literature, we know that elective neck dissection (END) is mandatory in clinically node-negative early oral cancers. However, this leads to overtreatment and morbidity in about 55-80% of patients. The emergence of recent level I evidence makes SNB the standard of care in this setting. However, its limitation of being a two-staged procedure, steep learning curve, the burden on resources, lack of infrastructure, short-lasting decrease in morbidity and lack of cost-effectiveness data limits its wide applicability. It is our routine departmental practice of performing limited neck dissection clearing level I-III/IV sparing level IIb which is cleared only if level IIa is metastatic. It is hypothesized that limited END would limit the morbidity of shoulder dysfunction and be a more feasible and cost-effective treatment option which could be a suitable alternative to SNB in this setting without compromising the survival outcomes. With this background, we propose to embark upon a phase III RCT comparing the oncologic outcomes and morbidity of SNB versus limited END. We hypothesize that limited END would have survival outcomes non-inferior, morbidity similar to SNB with higher cost-effectiveness.

Aims and objectives:

Aim To compare the survival outcomes, morbidity and cost-effectiveness of SNB versus limited END in node-negative early oral cancers

Primary objective

  • Overall survival

Secondary objectives

  • Shoulder morbidity (key secondary endpoint) longitudinally up to 2 years
  • Disease-free survival
  • Neck nodal recurrence-free survival
  • Other side effects (chyle leak, hematoma, lymphoedema)
  • Longitudinal Quality of life up to 2 years
  • Cost-effective analysis

Exploratory objectives Blood and tumour tissue will be collected and banked for biomarker studies. Exploratory analyses will be conducted at a later date. Efforts may be directed to identify the biomarkers to predict nodal metastasis.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age >18 years of age
  • Biopsy-proven invasive squamous cell carcinoma involving the site tongue and buccal mucosa
  • T1 and T2 lesions as per AJCC TNM 8 edition
  • Clinicoradiologically node negative
  • Amenable to per oral excision
  • Treatment naïve
  • No other site of malignancy

Exclusion criteria

  • Previous surgery in the head and neck region,
  • Upper alveolar or palatal lesions
  • Large heterogeneous leukoplakia or other premalignant lesions
  • Previous malignancy in the head and neck region
  • Patients requiring the free flap reconstruction

Treatment and study plan

Sentinel node biopsy

Procedure

The Sentinel node will be localized after injecting peritumoral nano colloid followed by dynamic lymphoscintigraphy and SPECT localization. Methylene blue or indocyanine green may be used but not mandatory as an adjunct for lymphoscintigraphy for node localization. Intraoperatively the node will be identified using a hand-held gamma probe. The sentinel node will be processed on a frozen section, histopathological processing with serial step sectioning, and immunohistochemistry. If reported as metastatic, then a single-stage or second-stage completion neck dissection will be performed.

Limited Elective Neck Dissection

Procedure

Patients who are allocated to the limited END arm will undergo dissection of level I, IIa and III/IV nodes sparing level IIb. Level IIa will be subjected to a frozen section and if reported as metastatic will mandate clearance of level IIb.

Primary outcomes

  1. Overall survival

    Time frame: 3 years

    Defined from the date of randomization to death due to any cause

Secondary outcomes

  1. Shoulder morbidity

    Time frame: Longitudinally at preoperatively, 3 months, at 6 months, 12 months and 24 months of treatment

    It will be assessed using the neck dissection impairment index (NDII). The range of movement of the shoulder will also be assessed using a goniometer

  2. Neck nodal recurrence

    Time frame: 3 years

    Defined from the date of randomization to isolated neck node recurrence or death due to any cause

  3. Disease free survival

    Time frame: 3 years

    Defined from the date of randomization to any recurrence (local, regional or distant metastasis) and second primary in the oral cavity

  4. Health related Quality of life

    Time frame: Longitudinally at preoperatively, 3 months, at 6 months, 12 months and 24 months of treatment

    Quality of life will be assessed using the European Organization for Research and Treatment of Cancer (EORTC) QLQ C30 and QLQ HN35 instruments

  5. Adverse events related to the surgical procedure and lymphedema

    Time frame: The lymphedema rating will be done at 3 months, at 6 months, 12 months and 24 months of treatment

    Details of the intra and perioperative delay including injury to critical structures, chyle leak, haemorrhage, and head and neck lymphedema

  6. Cost effectiveness

    Time frame: 3 years

    Based on direct cost comparison

Study contacts

Contact information is provided by the study sponsor or research team.

Richa Vaish, MS, M.Ch

CONTACT

[email protected]

02224177000 ext. 7238

Sponsors and collaborators

Lead sponsor

Tata Memorial Hospital

Other Gov

Collaborators

  • Tata Memorial Centre

Registry information

Official study title

Sentinel Node Biopsy Versus Limited Elective Neck Dissection in Early Cancers of Oral Cavity NoDe Negative (SECOND N0): Non-inferiority Phase III Trial

Acronym: SECOND N0

Important dates

Study start
2025
Primary completion
2032
Study completion
2034
First posted
Mar 17, 2023
Registry last updated
Jul 17, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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