Maximizing Lymph Node Dissection on Fresh and Fixed Lung Cancer Resection Specimens
Part of paid clinical trials in Boston, Massachusetts.
- Sponsor
- Brigham and Women's Hospital
- Study ID
- NCT06252129
- Status
- Recruiting
Conditions
- Lung Cancer
- Lymph Node Metastasis
- Pathologic Processes
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Accepted
Interventions
- Subjects undergoing a lung specimen lymph node dissection — OTHERA lobectomy specimen's resection will undergo systematic lymph node dissection either by the patient's treating thoracic surgeon and/or by a member of the pathology team. The protocol for a standardized lymph node dissection consists of a series of blunt peribronchial dissections starting from the hilum to the periphery, with particular attention to points of airway bifurcation where intrapulmonary lymph nodes aggregate. By emphasizing the intrapulmonary lymph node map and a standardized dissection, the team will remove more lymph nodes from the lobectomy specimen, resulting in an accurate N staging.
- Control group — OTHERControl group
Study Details
Lung cancer patients undergoing upfront surgery, highly benefit from a systematic lymph node dissection in the mediastinum and in the surgical specimens. The latter is performed by the pathologist. Developing a standardized technique to dissect the lobectomy specimen has the potential of maximizing the retrieval of all N1 stations lymph nodes. The investigators believe that the adoption of such technique will improve lung cancer staging and identify a higher number of patients that qualify for adjuvant therapies.
Key Dates
- Start date
- Jul 26, 2024
- Status verified
- Mar 2026
- Primary completion
- Jan 31, 2027
- Completion
- Dec 31, 2027
Study Design
- Enrollment
- 160 participants (estimated)
- Allocation
- NON_RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- DIAGNOSTIC
Arms
- Experimental: 1. Interventional groupsubjects who are being consented to this study and undergoing lymph node dissection as outlined in this protocol
- No Intervention: Concurrent non-interventional group
- Other: Retrospective cohort from 2021-2020
Primary Outcome Measure
Number of lymph nodes sampled [ Time Frame: 2 weeks ]
Central Contacts
- Paula Ugalde Figueroa, M.D.(617) 732-7696
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Brigham and Womens Hospital | Boston | Massachusetts | 02115 |
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