Anatomical Relationship of Level IB Lymph Nodes to the Submandibular Gland in Cancer Patients

Phase 1

Completed

• Conditions: Carcinoma
• Interventions: Procedure: neck dissection of at least the ipsilateral sub-level 1B

• Registration Number: NCT00728130
• Lead Sponsor: Southern Illinois University

Brief Summary

Hypothesis

1. The submandibular gland is not a lymphatic organ and usually remains uninvolved with head and neck cancer despite the presence of metastatic disease in the lymph nodes that surround it.

2. All the lymph nodes in the submandibular triangle can be removed without resection of the submandibular gland.

Study Design

A better understanding of the frequency of submandibular gland involvement may lead to refined treatment strategies for head and neck cancer, which can possibly spare removal of the submandibular gland and potentially improve the long term side effects from therapy.

Detailed Description

Hypothesis

1. The submandibular gland is not a lymphatic organ and usually remains uninvolved with head and neck cancer despite the presence of metastatic disease in the lymph nodes that surround it.

2. All the lymph nodes in the submandibular triangle can be removed without resection of the submandibular gland.

Study Design

1. A prospective controlled study.

2. A neck dissection of at least the ipsilateral sub-level 1B will be performed in all patients. In case of oral cavity tumors, about 15 minutes prior to the surgery, 1ml of Lymphazurin® blue dye will be injected in 4 quadrants around the primary site. The dissection will be performed in 3 stages. In the first stage all lymph node groups that lie either lateral, anterior, posterior, superior, or inferior to the submandibular gland, but within anatomical boundaries of level 1B, will be dissected. The submandibular gland will be left intact for this portion of the procedure. Next, the submandibular gland will be removed. Lastly, any remaining fibrofatty tissue that lies deep to the submandibular gland within the confines of level IB will be removed. Each lymph node group, the submandibular gland, and the fibrofatty tissue lying deep to the submandibular gland, will be submitted for pathological assessment in separate containers.

3. The following end-points will be measured: the number of lymph nodes identified within each lymph node group, the number of lymph nodes located within the submandibular gland, and the number of lymph nodes within the fibrofatty contents lying deep to the submandibular gland. The presence or absence of carcinoma within each of the assessed nodes will be documented, as well as extracapsular spread.

A better understanding of the frequency of submandibular gland involvement may lead to refined treatment strategies for head and neck cancer, which can possibly spare removal of the submandibular gland and potentially improve the long term side effects from therapy.

Study Timeline

• Study Start: 2008-05
• Study First Submitted: 2008-07-31
• Study First Submitted QC: 2008-08-04
• Study First Posted: 2008-08-05
• Primary Completion: 2010-01
• Study Completion: 2010-06
• Results First Submitted: 2013-05-29
• Results First Submitted QC: 2013-05-29
• Results First Posted: 2013-07-29
• Status Verified: 2014-12
• Last Update Submitted: 2014-12-12
• Last Update Posted: 2015-01-05

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 22

Inclusion Criteria

• Patients must have histologically or cytologically confirmed carcinoma of the oral cavity, oropharynx, larynx or hypopharynx
• Treatment of the regional lymph nodes to include neck dissection performed as the primary modality
• No previous treatment to the neck
• No previous treatment for the index cancer (surgery, chemotherapy, radiation or biological therapy)
• No known distant metastatic disease
• Age >/= 18
• The ability to understand and willingness to sign a study-specific written informed consent form
• Protocol treatment must begin </= 8 weeks of diagnostic biopsy

Exclusion Criteria

• Previous or concurrent head and neck primaries
• Prior surgery to study site other than biopsy
• Patients receiving any other treatment for cancer within 30 days previously
• Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia or psychiatric illness/social situations that would limit compliance with study requirements
• Known allergy to Lymphazurin®
• Pregnant or breast feeding females

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
A	neck dissection of at least the ipsilateral sub-level 1B	A neck dissection of at least the ipsilateral sub-level 1B will be performed in all patients

Primary Outcome Measures

Name	Time	Method
the Number of Lymph Nodes: 1. Identified Within Each Lymph Node Group, 2.Located Within the Submandibular Gland, and 3. Within the Fibrofatty Contents Lying Deep to the Submandibular Gland.	Post Surgical Time point	The number of head/ neck lymph nodes in pre-defined groups: Preglandular, Prevascular, Retrovascular, and Retroglandular as well as the number of nodes within the submandibular gland and within the fibrofatty contents lying deep to the submandibular gland.

Secondary Outcome Measures

Name	Time	Method
The Presence or Absence of Carcinoma Within Each of the Assessed Nodes Will be Documented, as Well as Extracapsular Spread.	Post surgical time point	Pathological detection of carcinoma within each of the dissected nodes reported as node groups.

Trial Locations

Locations (1)

SIU School of Medicine; 🇺🇸 Springfield, Illinois, United States