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corrected proof (abstract)
19 June 2016
Highlights
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- Stage FIGO IV accounts for 12–33% of all epithelial ovarian cancer.
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- Survival in FIGO IV did not change substantially over the past decades and is still less than 20% at 5 years.
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- Predictive markers for individualized therapy are missing, however complete tumor resection gains longer survival.
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- Balanced treatment decision models utilizing the achievable benefit while minimizing unnecessary treatment burden are proposed.
Epithelial
ovarian, fallopian tube and peritoneal cancer (EOC) is the seventh most
common cancer diagnosis among women worldwide and shows the highest
mortality rate of all gynecologic tumors. Different histological and
anatomic spread patterns as well as multiple gene-expression based
studies have demonstrated that EOC is indeed a heterogeneous disease.
The prognostic factors that best predict the survival in this disease
include: age, performance status and patient's comorbidities at the time
of diagnosis; tumor biology, histological type, amount of residual
tumor after surgery and finally tumor stage as surrogate for
pre-operative tumor burden and growth pattern. In the majority of
patients, the disease is diagnosed in advanced stage, disseminated
intra- and/or extra-abdominally. It is unclear whether this is a
consequence of distinct tumor biology, absence of anatomic barriers
between ovary and the abdominal cavity, delay of diagnosis and/or the
lack of sufficient early detection methods. FIGO stage IV disease,
defined as tumor spread outside the abdominal cavity (including
malignant pleural effusion) and/or visceral metastases, will be present
in 12–33% of the patients at initial diagnosis. Overall, median survival
for patients with stage IV disease ranges from 15 to 29 months, with an
estimated 5-year survival of approximately 20%. Unfortunately, over the
past decades the overall survival gain compared to stage III remains
disappointing.
The current review aims to summarize
the current data published in the international literature concerning
FIGO stage IV EOC and discusses the published evidence for the clinical
management of these patien
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