Aims. We initiated a Phase I feasibility study using a gamma-detecting prob
e (GDP) and radiolabelled colloid to localize the sentinel lymph node (SLN)
in breast cancer. The aim of the study was to establish the ideal timing f
or injection and examine any possible exclusion criteria for this method.
Methods. Thirty breast cancer patients diagnosed by fine needle aspiration
(FNA) were included in this study. All were injected with 60 MBq rhenium co
lloid labelled with Tc-99m (Tck-17). Scintigraphy was done 20 min, 2, 6 and
25 hours post-injection. Patients were then taken to surgery where they we
re injected with patent blue dye. During surgery, the SLN was located with
a CDP (Neoprobe(R) Model 1000). In 28 patients, the SLN was identified by s
cintigraphy 2 hours after injection, identical to the images seen after 24
hours.
Results. In all 28 patients, the SLN was found by the GDP during surgery. I
n 26 patients the SLN was dyed blue. The two patients with no SLN localizat
ion had received prior radiation. Pathology disclosed SLNs with metastases
in seven patients. Two patients had a negative SLN but had an axillary lymp
h node replaced by tumour.
Conclusions. Two to 24 hours prior to surgery is suitable timing for inject
ion. Previous radiotherapy predicts failure for this procedure. Further stu
dies are needed to find the exact false-negative rate of this method for br
east cancer.