Types of ovarian cancer
Ovarian cancer is classified into different types on the basis
of its histological appearance - that is, how it looks to the
pathologist through the microscope. The majority of ovarian cancers
fall within the category of epithelial ovarian cancer. The
remaining 10% consist of rare types.
Epithelial ovarian cancer
The greatest clinical challenge among gynaecological cancers.
Approximately 6900 new cases are diagnosed annually.Three-quarters
present with advanced disease, which has spread outside the
pelvis.
Within epithelial ovarian cancer (OvCa) there are six subtypes
(% frequency in brackets). Each is derived from a different type of
tissue in the lower genital tract (also known as the Mullerian
tract). However, within invasive cancers there is not a great deal
of difference in prognosis for the first three and the distinction
is mainly a pathological one.
Serous
This form accounts for around 70% of cases and is
therefore the most common type.
Mucinous
This accounts for a further 10%. These tumours have a slightly
worse prognosis than serous tumours.
Endometrioid
These tumours (5%) are more likely to be associated with disease
in the uterus (womb) and sometimes an ovary is found to be affected
when a woman is diagnosed with endometrial cancer.
Clear cell
These tumours (around 3-4%) have a poorer prognosis and tend to
behave more aggressively. Pathologists do not usually grade these
tumours since, whether they are Grade I, II or III, this tendency
exists and grade is not helpful in predicting prognosis.
Ovacome produces a factsheet that covers clear cell ovarian
cancer in more detail; click here
to download (pdf).
Borderline tumours
10-15% of ovarian cancers are borderline tumours, also known as
tumours of low malignant potential. They tend to remain confined to
the ovary for long periods and usually occur in premenopausal
women. Implants outside the ovary can arise but there is currently
no evidence that the course of this disease is altered by
chemotherapy. However, some novel treatments such as matrix
metalloproteinase inhibitors may well have a role: the difficulty
is establishing a trial in a group of patients with an uncommon
disease, as even somebody specialising in the treatment of ovarian
cancer will only see a handful of such patients a year.
Treatment of the different types of epithelial cancers is
essentially the same. In those fit to receive it the current gold
standard is Taxol and a platinum analogue (cisplatin or
carboplatin). This is based on the results of two randomised trials
conducted in North America and Europe.
Ovacome produces a factsheet that covers clear cell ovarian
cancer in more detail; click here to
download (pdf).
Germ cell tumours
Germ cell tumours of the ovary make up 3% of malignant ovarian
tumours, so they are rare, just one-tenth as common as germ cell
tumours of the testis. Hence advances in treatment have largely
developed through treatment of the testicular tumours which are of
the same origin - from the germ cells of the ovary - in other words
the cells that ultimately become eggs.
Germ cell tumours themselves are divided according to their main
cell type; they range from embryonal carcinoma at the most
undifferentiated end of the spectrum (in other words very immature
cells) via immature teratoma through to mature teratoma. The most
common type is a dysgerminoma, accounting for 30-40%. A detailed
discussion is not realistic within this space but if you have a
germ cell tumour of the ovary then you should be managed within a
specialist unit with particular experience. They tend to occur in
young women (the majority between 10 and 30 years) and adolescents
and if managed correctly usually have a good prognosis
The rare forms include:
- Dysgerminoma
- Endodermal sinus tumours
- Teratoma, immature, mature or mixed
- Embryonal carcinoma
- Choriocarcinoma
- Sex-cord stromal tumours (5-8%)
- Granulosa cell tumours
- Sertoli-Leydig tumours
- Sarcomas
Ovacome produces a factsheet that covers in more detail the
rarer forms of ovarian cancer; please click
here to download (pdf).