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Dose optimization for near‐infrared fluorescence sentinel lymph node mapping in patients with melanoma
Author(s) -
van der Vorst J.R.,
Schaafsma B.E.,
Verbeek F.P.R.,
Swijnenburg R.J.,
Hutteman M.,
Liefers G.J.,
van de Velde C.J.H.,
Frangioni J.V.,
Vahrmeijer A.L.
Publication year - 2013
Publication title -
british journal of dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.304
H-Index - 179
eISSN - 1365-2133
pISSN - 0007-0963
DOI - 10.1111/bjd.12059
Subject(s) - sentinel lymph node , indocyanine green , medicine , melanoma , biopsy , lymphadenectomy , nuclear medicine , lymph , sentinel node , lymph node , pathology , cancer , breast cancer , cancer research
Summary Background Regional lymph node involvement is the most important prognostic factor in cutaneous melanoma. As only 20% of patients with melanoma have occult nodal disease and would benefit from a regional lymphadenectomy, the sentinel lymph node (SLN) biopsy was introduced. Near‐infrared (NIR) fluorescence has been hypothesized to improve SLN mapping. Objectives To assess the potential of intraoperative NIR fluorescence imaging to improve SLN mapping in patients with melanoma and to examine the optimal dose of indocyanine green adsorbed to human serum albumin (ICG:HSA). Methods Fifteen consecutive patients with cutaneous melanoma underwent the standard SLN procedure using 99m technetium‐nancolloid and patent blue. In addition, intraoperative NIR fluorescence imaging was performed after injection of 1·6 mL of 600, 800, 1000 or 1200 μmol L −1 of ICG:HSA in four quadrants around the primary excision scar. Results NIR fluorescence SLN mapping was successful in 93% of patients. In one patient, no SLN could be identified using either conventional methods or NIR fluorescence. A total of 30 SLNs (average 2·0, range 1–7) were detected, 30 radioactive (100%), 27 blue (73%) and 30 NIR fluorescent (100%). With regard to the effect of concentration on signal‐to‐background ratios a trend ( P = 0·066) was found favouring the 600, 800 and 1000 μmol L −1 groups over the 1200 μmol L −1 group. Conclusion This study demonstrates feasibility and accuracy of SLN mapping using ICG:HSA. Considering safety, cost and pharmacological characteristics, an ICG:HSA concentration of 600 μmol L −1 appears optimal for SLN mapping in cutaneous melanoma, although lower doses need to be assessed.