Overexpression of MPS antigens by squamous cell carcinomas of the head andneck: Immunohistochemical and serological correlation with FDG positron emission tomography
Bc. Stack et al., Overexpression of MPS antigens by squamous cell carcinomas of the head andneck: Immunohistochemical and serological correlation with FDG positron emission tomography, ANTICANC R, 19(6C), 1999, pp. 5503-5510
Survival from advanced primary or recurrent Squamous Cell Carcinoma (SCC) o
f the head and neck (H&N) is poor. More accurate detection of primary tumor
s and recurrence may provide ways to improve survival. No standard serum tu
mor marker is routinely used for surveillance of SCC-H&N. In this paper, we
evaluated the performance characteristics of the MPS-H tumor marker test f
or the quantitative measurement of "MPS-H" heat-generated immunoreactive pr
oteins and assessed the clinical utility of this marker in the detection an
d monitoring of SCC-H&N. In approximately 92% of the subjects having no evi
dence of SCC-H&N, the MPS-H levels were lower than 15 ng/mL. In 76% of pati
ents having SCC-H&N at,various stages (T1-T4), the MPS-H level was > 15 ng/
mL (range: 20-200 ng/mL). In addition, we found a statistically significant
correlation between PET positive cases and high MPS-H serum levels in SCC-
H&N patients with recurrent disease. These results suggest that MPS-H may p
rovide an initial screening test that would allow for selective PET imaging
in these patients. Furthermore, we found that there was greater expression
of MPS-1 in tumors of higher histological grades. Thus, in tumors with mor
e histological agressiveness there is mom MPS-1, indicating the potential u
sefulness of this marker in prognosis for. SSC-H&N. Considering the immunoh
istochemical, serological, and FDC-PET data presented here, and the compell
ing need to expedite the early diagnosis of primary and recurrent epithelia
l malignancies of the head and neck, we are further evaluating the system o
f MPS antigens in a large patient population as a tool for the early serolo
gic and histologic diagnosis of SCC-H&N.