With the advent of new therapeutic modalities, the treatment options for on
cologists can vary greatly depending upon the aggressiveness of the patient
's cancer. Patients may receive no therapy, adjuvant therapy, aggressive ad
juvant therapy (taxane based), monoclonal antibody therapy (e.g. Herceptin)
or bone marrow transplantation. It is now mandatory to determine accurate
prognostic patient profiles at diagnosis and during therapy to determine wh
o would benefit most from a particular therapeutic regimen or to determine
who should be shifted into more aggressive therapy. We now have ultra-sensi
tive methods of tumor cell detection that can determine the presence of min
imal residual cancer (MRC) in marrow, stem cell product (SCP) and lymph nod
e to help create these prognostic profiles. The author has conducted a crit
ical review of the literature regarding the type of testing used to detect
MRC, the incidence of MRC in marrow, SCP, and lymph node, and the clinical
significance of MRC at diagnosis and during therapy.
To date it is now clear that immunohistochemistry is a very useful diagnost
ic tool with adequate sensitivity to detect MRC. The presence of MRC at dia
gnosis in marrow and/or lymph node is associated with a poor prognosis for
a number of disorders including breast cancer, neuroblastoma, gastrointesti
nal tumors, and lung cancer. In addition, the presence of MRC during therap
y in marrow and/or SCP is associated with a very poor prognosis for patient
s with breast cancer. The use of testing for MRC in the patient provides pr
ognostic information that may be of use to the oncologist.