158
Cirutiuns from
the Literature
Epidermal growth factor receptor expression in normal ovarian
times the risk of positive peritoneal
epithelium and ovarian cancer. II. Relationship between receptor
Seventy-four
expression and response to epidermal growth factor
cytology were stage IC or more. In contrast.
Rodriguez
GC;
Clarke-Pearson
Berchuck DL;
Duke University 27710, AM
A; Whitaker
RS; Schlossman
D;
with normal
Center. PO Box 3079,
Durham.
NC
GYNECOL
1991. l64/3 (745-750)
Previously we have shown that epidermal In this study we examined
growth
factor
on
proliferation
epithelial cells in monolayer
of
normal
of epidermal
human
ovarian
culture. We found that epidermal increases in pro-
Serial
of
tagged
high-affinity
analysis of binding of epider-
with
iodine
receptors
125
in
all
indicated
of
the
the
ovarian
epithelial ceils and ovarian cancer cell lines. The number and affmity of receptors was similar in the normal epithelium cancer cell lines, and there was no relationship epidermal
factor
growth
receptor factor.
number
and
We conclude
endometrial
advanced-stage
tumor,
and
and
between epider-
responsiveness
that
human
to
ovarian
125 levels during chemotherapy
for metastatic
or
Fanning J; Piver MS School q/‘Medicinc~. PO Box 19230, Springfield, USA
factor
or IB. Patients
Division c?f’ Gynecologic Oncology, Southc+-n Illinois
OBSTET
mal growth
were stage IA
who have malignant
are more likely to require extended surgical staging.
CA
< 0.01). In addition, growth
cervical
70% of patients
recurrent endometrial cancer
liferation in epithelial cells from each of five normal ovaries (p Scatchard
malignant
cells detected by cervical cytology are at increased risk of havtherefore
cancer cells in
the effect
growth factor stimulated twofold to fourfold
presence
carcinoma
with
growth factor acts
for some, but not all, ovarian
culture.
washings (33 versus 10%).
patients
ing a deeply invasive. high-grade,
USA
J OBSTET
as a mitogen
mal
of
cervical cytology
with endometrial
Bast RC Jr
Medical
percent
GYNECOL
Universiiy.
IL 62794-9230.
1991, 77/2 (278-280)
The purpose of this study was to evaluate the role of serial CA
125 in monitoring
disease status during chemotherapy
women with metastatic
or recurrent
endometrial
cancer.
in CA
125 was measured in 21 women receiving cisplatin. etoposide. and Adriamycin
for a total of 275 courses of chemotherapy
(median eight). Eight of ten patients had elevated pre-therapy CA 125 levels (median 233 U/mL).
CA
I25 became and/or
re-
epithelial cells normally express epidermal growth factor recep-
mained negative in all 20 women with responding or stable dis-
tors and that epidermal
ease and was elevated in all nine patients who relapsed.
growth
these cells. Although
factor acts as a mitogen
the mitogenic
growth factor often is attenuated
response
in ovarian
for
to epidermal
cancer cell lines,
median level at the time of relapse was 56 U/mL.
elevated before clinical relapse in five of nine patients (56%).
loss of responsiveness to epidermal growth factor does not ap-
Serial CA 125 may aid in the management
pear to be due to decreased receptor expression.
chemotherapy
B; Warshal
Raubertas
RF
Dqwrlment
uf
DP; Angel C; Dvoretsky and
Rochester School c$ Medicine, GYNECOL
Gymwlugy,
Srrong Mcmoriul
Elmwuod Avenue, Rochester, NY OBSTET
14642.
Medicul
Huspirul, 601
OBSTET
carcinoma.
preoperative
prognostic
factors
is helpful
therapy.
Extended
surgical
staging,
including
node dissection, is indicated invasion or high-grade
factors for extrauterine
iden-
in planning pelvic
in patients
and
with deep
Centw.
und Gynccolo~y,
GYNECOL
1991. 7712 (276-277) families were identified.
for 24 cases. Five first-degree relatives underwent oophorectomy,
and early ovarian carcinoma
one of them. Familial
aggregation
prophylactic
was diagnosed in
of ovarian cancer occurs in
carci-
Prognostic factors in stage IB squamous cervical cancer patients with low risk for recurrence Smiley LM; Burke TW; Silva EG; Morris Wharton
cytology was normal in 20 patients (23%). whereas suspicious
Dcpurtmem
or malignant endometrial
Cwkr.
cells were present in 23 and 43 cases Suspicious
or malignant
cytology was associated with deeper myometrial tumor
origin,
accounting
the Israeli Jewish population.
noma, all of whom underwent surgical staging, to correlate the
.01 I), higher postoperative
The Chuim Shcha
Td Hushomc~r. ISR
cytologic results with surgical and pathologic findings. Cervical
respectively.
cancer.
tumor, or when other risk
spread are present. In this study, cervi-
cal cytology was reviewed in 86 patients with endometrial
(27 and 50%).
of women receiving endometrial
G
of Ohsrelrics
eight ovarian cancer-prone
of poor
or recurrent
Among 310 women with ovarian cancer of epithelial
1991, 7713 (458-462)
In patients with endometrial
myometrial
Menczer J: Ben-Baruch
u/
Universily
USA
tification periaortic
PM; Lin JY;
Depurrmcnr 0hsietric.v
for advanced
Familial ovarian cancer in Israeli Jewish women
Endometrial carcinoma: The relevance of cervical cytology DuBeshter
The
Levels were
cervical
invasion (P =
grade (P = .006),
positive
OBSTET About
M; Gershenson
DM;
JT of Gynecology.
1515 Holcomhr GYNECOL one-half
Box
Boulevard,
67,
MD
An&won
How~on.
Cuncer
TX 77030.
USA
1991. 77/2 (271-275) of cervical
cancer
patients
whose tumors
recur after radical surgery have negative lymph nodes and clear
peritoneal washings (P = ,012). and more advanced stage by In-
resection margins. We evaluated 95 patients with squamous cell
ternational
tumors who underwent
= ,024).
Federation
of Gynecology
When compared
and Obstetrics criteria (P
with patients
with normal
cervical
cytology, those who had malignant
endometrial
cells had over
twice the risk of deep myometrial
invasion (67 versus 30%).
twice the risk of grade 2 or 3 tumor (60 versus 30%). and three
Inr J Gynecol Ohstrt 37
phadenectomy
radical
between January
who were thought
hysterectomy
and pelvic lym-
1975 and December
1985 and
to be at low risk for recurrence
whether other clinical or histopathologic tive of tumor recurrence.
Detailed
to see
factors were predic-
retrospective
record review