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Published on: August 19, 2021
Drug evaluation: Lymphoseek - Neoprobe's sentinel lymph node imaging agent for use in cancer patients
1Lntdp@earthlink.net
Abstract:
Neoprobe, under license from the University of California San Diego Cancer Center, is developing 99mTc-DTPA-mannosyl-dextran (Lymphoseek) as a potential agent for imaging lymph nodes in patients undergoing treatment for breast cancer and melanoma. Phase II trials of Lymphoseek were initiated in mid 2006.
Insights
Neoprobe is developing 99mTc-DTPA-mannosyl-dextran (Lymphoseek) for lymph node imaging in breast cancer and melanoma patients. Phase II trials began in 2006 to assess its potential as a diagnostic agent.
Area of Science:
- Oncology
- Radiopharmaceuticals
- Medical Imaging
Background:
- Accurate lymph node imaging is crucial for staging and treatment monitoring in breast cancer and melanoma.
- Current imaging techniques may have limitations in sensitivity and specificity for detecting lymph node involvement.
- Neoprobe is developing a novel imaging agent to address these challenges.
Purpose of the Study:
- To evaluate the potential of 99mTc-DTPA-mannosyl-dextran (Lymphoseek) as an imaging agent for lymph nodes.
- To assess the utility of Lymphoseek in patients undergoing treatment for breast cancer and melanoma.
Main Methods:
- Development of 99mTc-DTPA-mannosyl-dextran (Lymphoseek) by Neoprobe.
- Initiation of Phase II clinical trials in mid-2006.
- Licensing agreement with the University of California San Diego Cancer Center.
Main Results:
- Phase II trials were initiated in mid-2006, indicating progress in clinical evaluation.
- The abstract does not contain specific results from the trials, only the initiation status.
Conclusions:
- Lymphoseek shows promise as a potential diagnostic agent for lymph node imaging.
- Further clinical evaluation through Phase II trials is underway to determine its efficacy and safety.
