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Multimodal surgical guidance towards the sentinel node in vulvar cancer.

H M Mathéron ,
N S van den Berg ,
O R Brouwer ,
G H Kleinjan ,
W J van Driel ,
J W Trum ,
E Vegt ,
G Kenter ,
F W B van Leeuwen ,
R A Valdés Olmos

Abstract

MATERIALS AND METHODS

Fifteen patients with vulvar cancer (29 groins) scheduled for SN biopsy were peritumorally injected with ICG-(99m)Tc-nanocolloid followed by lymphoscintigraphy and SPECT/CT imaging to identify the SNs. In thirteen patients, shortly before the start of the operation, blue dye was intradermally injected around the lesion. SNs were harvested using a combination of radiotracing, fluorescence imaging, and optical blue dye detection. A portable gamma camera was used before and after SN excision to confirm excision of the preoperatively defined SNs.

CONCLUSION

ICG-(99m)Tc-nanocolloid can be used for preoperative SN identification and enables multimodal (radioactive and fluorescent) surgical guidance in patients with vulvar cancer. The addition of fluorescence-based optical guidance offers more effective SN visualization compared to blue dye.

RESULTS

Preoperative lymphoscintigraphy and SPECT/CT imaging visualized drainage to 39 SNs in 28 groins. During the operation, 98% (ex vivo 100%) of the SNs were radioactive. With fluorescence imaging 96% of the SNs (ex vivo 100%) could be visualized. Only 65% of the SNs had stained blue at the time of excision.

INTRODUCTION

Conventional sentinel node (SN) mapping is performed by injecting a radiocolloid followed by lymphoscintigraphy (and SPECT/CT imaging). An extra intraoperative injection with blue dye can then allow for optical identification of the SN. In order to improve the current clinical standard, the hybrid tracer indocyanine green (ICG)-(99m)Tc-nanocolloid was introduced, a tracer that is both radioactive and fluorescent. This feasibility study aimed to evaluate the value of a multimodal-based SN biopsy in vulvar cancer.

More about this publication

Gynecologic oncology

Volume 131
Issue nr. 3
Pages 720-5
Publication date 01-12-2013

Full text links

Publisher website (DOI) 10.1016/j.ygyno.2013.09.007
Europe PubMed Central 24051219
Pubmed 24051219

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