Volume 125, Issue 4 pp. 712-718
MELANOMA/SARCOMA

How much time is enough? Sentinel lymph node mapping time depends on the radiotracer agent

Austin Eckhoff MD

Austin Eckhoff MD

Department of Surgery, Duke University, Durham, North Carolina, USA

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Norma E. Farrow MD

Norma E. Farrow MD

Department of Surgery, Duke University, Durham, North Carolina, USA

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Caitlin Silvestri MD

Caitlin Silvestri MD

Department of Surgery, Sidney Kimmel Medical College at Thomas Jefferson University, Philadelphia, Pennsylvania, USA

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Emily Stroobant MD

Emily Stroobant MD

Department of Surgery, Sidney Kimmel Medical College at Thomas Jefferson University, Philadelphia, Pennsylvania, USA

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Charles Intenzo

Charles Intenzo

Department of Nuclear Medicine, Thomas Jefferson University Hospital, Philadelphia, Pennsylvania, USA

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Margaret Leddy PA-C

Margaret Leddy PA-C

Department of Surgery, Duke University, Durham, North Carolina, USA

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Douglas S. Tyler MD

Douglas S. Tyler MD

Department of Surgery, University of Texas Medical Branch, Galveston, Texas, USA

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Adam Berger MD

Adam Berger MD

Rutgers Cancer Institute, New Brunswick, New Jersey, USA

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Georgia M. Beasley MD

Corresponding Author

Georgia M. Beasley MD

Department of Surgery, Duke University, Durham, North Carolina, USA

Duke Cancer Institute, Duke University, Durham, North Carolina, USA

Correspondence: Georgia M. Beasley, MD, Duke University, DUMC 3118, Erwin Rd, Durham, NC 27710, USA.

Email: [email protected]

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First published: 17 November 2021
Citations: 1

Abstract

Background

In 2014, technetium-99m tilmanocept (TcTM) replaced technetium-99m sulfur colloid (TcSC) as the standard lymphoscintigraphy (LS) mapping agent in melanoma patients undergoing sentinel lymph node biopsy (SLNB). The aim of this study was to examine differences in mapping time, intra-operative identification of sentinel lymph node (SLN), and false negative rate (FNR) between patients who underwent SLNB with TcTM compared to TcSC.

Methods

Patients who underwent SLNB between 2010 and 2018 were retrospectively identified. Patient demographic, tumor, and imaging data was stratified by receipt of TcSC (n = 258) or TcTM (n = 133). Student's t test and χ2 test were used to compare characteristics and outcomes.

Results

Both cohorts were similar in demographic, primary tumor characteristics, and total number of SLN identified (TcTM 3.56 vs. TcSC 3.28, p = 0.244). TcTM was associated with significantly shorter LS mapping times (51.8 vs. 195.1 min, p < 0.01). There was no significant difference in the number of patients with positive SLN (TcTM 11.3 vs. TcSC 17.4%, p = 0.109) and the FNR was similar between both groups (TcTM 25% vs. TcSC 22%).

Conclusion

TcTM was associated with significantly shorter LS mapping time while identifying similar numbers of SLN. Our results support further study to ensure similar FNR and oncologic outcomes between agents.

CONFLICT OF INTERESTS

Georgia M. Beasley: advisory board Regeneron (2020), Cardinal Health (2018). Berger-Advisory Board, Cardinal Health.

DATA AVAILABILITY STATEMENT

Due to the nature of this study, participants of this study did not agree for their data to be shared publicly, so supporting data is not available.

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.