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FALSE-NEGATIVE RATE IN INDENTIFYING AXILLARY NODE METASTASES
In one of the original Ludwig node-negative chemotherapy trials,
there were 900 patients who later had enhanced pathology on their
nodes (serial sectioning or more sections done with H&E staining),
10 to 15 percent of them actually had positive disease in those
axillary lymph nodes. When we give our pathologists 20 lymph nodes,
what usually happens is that maybe one or two slices are taken.
Sometimes lymph nodes are missed completely; we ask them to go back
and re-gross the specimen and they find six more lymph nodes. So,
the false-negative rate is absolutely understandable.
When I give my pathologist one or two sentinel lymph nodes, they
can afford to do serial sectioning or at least more sections through
the node. And if they are negative on H&E staining, they can
then afford to do immunohistochemistry. Weve known that with
small node-negative breast cancers, 10 to 15 percent will fail systemically.
And now here we are 10 years later saying, Gee, 10 to 15 percent
werent node-negative. They were actually node-positive originally.
So, one of the challenges is to find out whether the group
that recurs systemically is the group that was misclassified as
node-negative originally, and that work is going on right now.
Patrick Borgen, MD
International (Ludwig) Breast Cancer Study Group. Prognostic
importance of occult axillary lymph node micrometastases from breast
cancers. Lancet 1990;335-1565. Abstract
DCIS & SENTINEL LYMPH NODE BIOPSY
We divide DCIS patients into high-risk and low-risk.High-risk winds
up being about 30 percent of our cases low--risk, 70 percent.
We perform sentinel node mapping only in the high-risk group
defined as a breast filled with DCIS, (where you re doing
a mastectomy) palpable DCIS or DCIS with a mass on mammogram. These
would be patients in whom we would definitely perform a sentinel
node biopsy. If we have H&E disease in the sentinel node and
still no invasive carcinoma in the breast, thats treated as
N1 disease. At the other end of the spectrum, a single cell on IHC
in a patient with DCIS, more often than not is not treated as N1
disease. These are taken on a case-by-case basis. Thankfully, we
only get positive nodes in 10 percent of our high-risk DCIS population
or three percent of our total DCIS population. So, dealing with
IHC-only positive disease in a lymph node and DCIS is a very rare
event less than one in 100 cases.
Many people have argued that in DCIS, serially sectioning the breast
is the best way to look for invasion.We argue that its not
that doing a sentinel node biopsy, looking for that metastatic
cluster, is actually a better way to rule out invasion.
In the patient with an invasive carcinoma its a different
story, because there, the majority of our patients, by virtue of
having tumors greater than a centimeter, are destined to receive
cytotoxic chemotherapy anyway. So, what were looking at is
a small subset of patients with subcentimeter cancers, who have
these cells in these lymph nodes. And again, thankfully, its
a very small subset of our patients.
Patrick Borgen, MD
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