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Sentinel Node Biopsy Versus Limited Elective Neck Dissection in Early Cancers of Oral Cavity NoDe Negative (SECOND N0)

Primary Purpose

Mouth Neoplasms

Status
Not yet recruiting
Phase
Not Applicable
Locations
India
Study Type
Interventional
Intervention
Sentinel Node Biopsy
Limited Elective Neck Dissection
Sponsored by
Tata Memorial Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Mouth Neoplasms focused on measuring mouth neoplasms, neck dissection, sentinel lymph node biopsy, survival, morbidity

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • Tata Memorial Centre

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Sentinel node biopsy

Limited elective neck dissection

Arm Description

Outcomes

Primary Outcome Measures

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

Secondary Outcome Measures

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
Neck nodal recurrence
Defined from the date of randomization to isolated neck node recurrence or death due to any cause
Disease free survival
Defined from the date of randomization to any recurrence (local, regional or distant metastasis) and second primary in the oral cavity
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
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
Cost effectiveness
Based on direct cost comparison

Full Information

First Posted
March 7, 2023
Last Updated
March 17, 2023
Sponsor
Tata Memorial Hospital
Collaborators
Tata Memorial Centre
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1. Study Identification

Unique Protocol Identification Number
NCT05774483
Brief Title
Sentinel Node Biopsy Versus Limited Elective Neck Dissection in Early Cancers of Oral Cavity NoDe Negative
Acronym
SECOND N0
Official Title
Sentinel Node Biopsy Versus Limited Elective Neck Dissection in Early Cancers of Oral Cavity NoDe Negative (SECOND N0): Non-inferiority Phase III Trial
Study Type
Interventional

2. Study Status

Record Verification Date
March 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
April 2023 (Anticipated)
Primary Completion Date
April 2032 (Anticipated)
Study Completion Date
April 2034 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Tata Memorial Hospital
Collaborators
Tata Memorial Centre

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
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.
Detailed Description
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 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Mouth Neoplasms
Keywords
mouth neoplasms, neck dissection, sentinel lymph node biopsy, survival, morbidity

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
508 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Sentinel node biopsy
Arm Type
Active Comparator
Arm Title
Limited elective neck dissection
Arm Type
Experimental
Intervention Type
Procedure
Intervention Name(s)
Sentinel Node Biopsy
Intervention Description
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.
Intervention Type
Procedure
Intervention Name(s)
Limited Elective Neck Dissection
Intervention Description
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 Outcome Measure Information:
Title
Overall survival
Description
Defined from the date of randomization to death due to any cause
Time Frame
3 years
Secondary Outcome Measure Information:
Title
Shoulder morbidity
Description
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
Title
Neck nodal recurrence
Description
Defined from the date of randomization to isolated neck node recurrence or death due to any cause
Time Frame
3 years
Title
Disease free survival
Description
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
Title
Health related Quality of life
Description
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
Title
Adverse events related to the surgical procedure and lymphedema
Description
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
Title
Cost effectiveness
Description
Based on direct cost comparison
Time Frame
3 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Richa Vaish, MS, M.Ch
Phone
02224177000
Ext
7238
Email
drvaishricha@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Richa Vaish, MS, M.Ch
Organizational Affiliation
Tata Memorial Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Tata Memorial Centre
City
Mumbai
State/Province
Maharashtra
ZIP/Postal Code
400012
Country
India
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Richa Vaish, MS, M.Ch
Phone
022-24177000
Ext
7238
Email
drvaishricha@gmail.com

12. IPD Sharing Statement

Citations:
PubMed Identifier
35988294
Citation
Vaish R, Mittal N, Mahajan A, Rane SU, Agrawal A, D'Cruz AK. Sentinel node biopsy in node negative early oral cancers: Solution to the conundrum! Oral Oncol. 2022 Nov;134:106070. doi: 10.1016/j.oraloncology.2022.106070. Epub 2022 Aug 18.
Results Reference
background
PubMed Identifier
26027881
Citation
D'Cruz AK, Vaish R, Kapre N, Dandekar M, Gupta S, Hawaldar R, Agarwal JP, Pantvaidya G, Chaukar D, Deshmukh A, Kane S, Arya S, Ghosh-Laskar S, Chaturvedi P, Pai P, Nair S, Nair D, Badwe R; Head and Neck Disease Management Group. Elective versus Therapeutic Neck Dissection in Node-Negative Oral Cancer. N Engl J Med. 2015 Aug 6;373(6):521-9. doi: 10.1056/NEJMoa1506007. Epub 2015 May 31.
Results Reference
background
PubMed Identifier
26672853
Citation
Vaish R, Gupta S, D'Cruz AK. Elective versus Therapeutic Neck Dissection in Oral Cancer. N Engl J Med. 2015 Dec 17;373(25):2477. doi: 10.1056/NEJMc1511351. No abstract available.
Results Reference
background
PubMed Identifier
33877855
Citation
Hasegawa Y, Tsukahara K, Yoshimoto S, Miura K, Yokoyama J, Hirano S, Uemura H, Sugasawa M, Yoshizaki T, Homma A, Chikamatsu K, Suzuki M, Shiotani A, Matsuzuka T, Kohno N, Miyazaki M, Oze I, Matsuo K, Kosuda S, Yatabe Y; HNCMM Research Group. Neck Dissections Based on Sentinel Lymph Node Navigation Versus Elective Neck Dissections in Early Oral Cancers: A Randomized, Multicenter, and Noninferiority Trial. J Clin Oncol. 2021 Jun 20;39(18):2025-2036. doi: 10.1200/JCO.20.03637. Epub 2021 Apr 20.
Results Reference
background
PubMed Identifier
33052754
Citation
Garrel 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.
Results Reference
background
PubMed Identifier
31611612
Citation
Hutchison IL, Ridout F, Cheung SMY, Shah N, Hardee P, Surwald C, Thiruchelvam J, Cheng L, Mellor TK, Brennan PA, Baldwin AJ, Shaw RJ, Halfpenny W, Danford M, Whitley S, Smith G, Bailey MW, Woodwards B, Patel M, McManners J, Chan CH, Burns A, Praveen P, Camilleri AC, Avery C, Putnam G, Jones K, Webster K, Smith WP, Edge C, McVicar I, Grew N, Hislop S, Kalavrezos N, Martin IC, Hackshaw A. Nationwide randomised trial evaluating elective neck dissection for early stage oral cancer (SEND study) with meta-analysis and concurrent real-world cohort. Br J Cancer. 2019 Nov;121(10):827-836. doi: 10.1038/s41416-019-0587-2. Epub 2019 Oct 15. Erratum In: Br J Cancer. 2022 Mar;126(5):831.
Results Reference
background
PubMed Identifier
32669674
Citation
Dhar H, Vaish R, D'Cruz AK. Comment on "Nationwide randomised trial evaluating elective neck dissection for early-stage oral cancer (SEND study) with meta-analysis and concurrent real-world cohort.". Br J Cancer. 2020 Sep;123(7):1198-1199. doi: 10.1038/s41416-020-0981-9. Epub 2020 Jul 16. No abstract available.
Results Reference
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Sentinel Node Biopsy Versus Limited Elective Neck Dissection in Early Cancers of Oral Cavity NoDe Negative

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