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abstract
Purpose of review: The purpose of this study is to summarize
the contemporary understanding of low-grade epithelial ovarian cancers.
Recent findings: Low-grade serous ovarian cancer is
biologically distinct from high-grade serous ovarian cancer. It is
associated with a high incidence of K-RAS and B-RAF mutations. Although
described as indolent due to median progression-free and overall
survivals of 20 and 99 months, respectively, with a median age of
diagnosis of 43 years, it accounts for a significant number of
patient-years lost. Retrospective studies suggest response rates of 5%
for chemotherapy and 9% for antioestrogen therapy. A prospective study
of the mitogen-activated protein kinase kinase inhibitor selumetinib
(response rate 15%) and retrospective bevacizumab studies suggest that
these may be more effective approaches.
Limited retrospective clinical data and even more sparse
molecular data suggest that similar distinctions may exist between
low-grade endometrioid and mucinous ovarian cancers and their respective
high-grade counterparts, but more research is required in order to
clarify the biological differences and the implications that these have
for management.
Summary: The results of phase III mitogen-activated
protein kinase kinase inhibitor studies in low-grade serous ovarian
cancer and further clinical and biological assessment of low-grade
endometrioid and mucinous ovarian cancers are urgently required.
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