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.
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 1\) Overall survival Secondary objectives 1. Shoulder morbidity (key secondary endpoint) longitudinally up to 2 years 2. Disease-free survival 3. Neck nodal recurrence-free survival 4. Other side effects (chyle leak, hematoma, lymphoedema) 5. Longitudinal Quality of life up to 2 years 6. 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.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
508
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.
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.
Tata Memorial Hospital
Mumbai, Maharashtra, India
RECRUITINGACTREC
Navi Mumbai, Maharashtra, India
NOT_YET_RECRUITINGMpmmcc & Hbch
Varanasi, Uttar Pradesh, India
NOT_YET_RECRUITINGOverall survival
Defined from the date of randomization to death due to any cause
Time frame: 3 years
Shoulder morbidity
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
Time frame: Longitudinally at preoperatively, 3 months, at 6 months, 12 months and 24 months of treatment
Neck nodal recurrence
Defined from the date of randomization to isolated neck node recurrence or death due to any cause
Time frame: 3 years
Disease free survival
Defined from the date of randomization to any recurrence (local, regional or distant metastasis) and second primary in the oral cavity
Time frame: 3 years
Health related Quality of life
Quality of life will be assessed using the European Organization for Research and Treatment of Cancer (EORTC) QLQ C30 and QLQ HN35 instruments
Time frame: Longitudinally at preoperatively, 3 months, at 6 months, 12 months and 24 months of treatment
Adverse events related to the surgical procedure and lymphedema
Details of the intra and perioperative delay including injury to critical structures, chyle leak, haemorrhage, and head and neck lymphedema
Time frame: The lymphedema rating will be done at 3 months, at 6 months, 12 months and 24 months of treatment
Cost effectiveness
Based on direct cost comparison
Time frame: 3 years
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