John Hopkins Medicine |
Most-and
possibly all ovarian cancer originates not in ovaries, but instead in the
distal end of fallopian tubes attached to them, reports the findings of
multi-center ovarian cancer genetics study published October 17, 2017 in Journal
Nature Communications.
Douglas A.
Levine, MD, director of the Division of Gynecologic Oncology at Perlmutter and
professor of Obstetrics and Gynecology at NYU School of Medicine said in a news release, "Based on a better understanding of its origins, our study
suggests new strategies for the prevention and early detection of ovarian
cancer."
Serous tubal
intra-epithelial carcinoma (STIC) are identified as precursors in ~50%
cases of advanced high-grade serous carcinomas (HGSCs) of the pelvis. STIC have
helped us a lot in understanding the origin of ovarian malignancies. It was originally
diagnosed in fimbrial part fallopian tube when researchers examined the serial
sections of this area in tube samples in cases of women who underwent prophylactic
bilateral salpingo-oophorectomy(BSO).
This
discovery led researchers to identify many cases of presumed ovarian cancer to
be of tubal origin because of presence of a STIC.
The
researchers in this study identified a total of 96 bio specimens’ samples, with
or without STIC.
The median age of the women was 59 years, with majority being Caucasians,
with nearly 50% of women in FIGO stage IIIC and all women had HGSCs. Presence or
absence of STIC did not change the clinical features or median survival.
In depth a
morphologic, immunohistochemical, and molecular analysis of the samples failed
to identify any difference in genetic profile of cells from HGSCs vs those from
STIC in fallopian tube.
"We
found no differences in the 20,000 genes that we can identify," says Levine.
"This leads us to believe that that these ovarian cancers all originate in
the fallopian tubes."
In fact, HGSCs
had molecular profiles more similar to normal fallopian tube epithelium than to
ovarian surface epithelium or peritoneum.
This study
findings have several implications for early diagnosis of ovarian malignancy.
If biomarkers can be identified on these tubal cells, then one day we may be
able to diagnose ovarian malignancy by blood test. Since the tube is connected
to the uterus, direct tissue sampling can also be carried out in future.
If the study
finding is confirmed, then only removing the tubes may reduce the women’s risk
of ovarian malignancy in patients with BRCA1 and 2 mutations. In fact, the NYU
Langone Health center is currently participating
in a study Women Choosing Surgical Prevention or WISP trial,
which is comparing the quality of life in women who have undergo only salpingectomy as compared to salpingo-oophorectomy.
The researchers
believe that it may take years before the study findings are confirmed and
translate into actual clinical practice. But, at this stage the study holds a
lot of meaning for gynecological oncologists and the evidence is sufficient to
support incidental salpingectomy in average-risk women.
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