Limitations
in the study. Owing to the study design, there may
be a possibility of quality problems in the preserved serum.
The sample distribution was limited and different from those
of other investigations. The cut-off of HE4 is not determined
and varies among comparable reports. Indeed, the history of
HE4 is relatively short and HE4 is subject to clinical validation.
Therefore, both HE4 and CA-125 should be included in more
prospective studies in the future.
In another paper in this issue, Kang et al. [12] dealt with the
utilization of CA-125 as a predictive marker for recurrence.
They collected data from two high-volume institutions and
scrutinized the correlation between post-treatment nadir CA-
125 and progression free survival in patients with advanced
ovarian cancer who had achieved complete remission. An
acknowledgeable finding of this paper is the determination of
a reasonable cut-off value of CA-125 that can be used for the
identification of high-risk patients. Although there were some
Limitations
including sample size and population, the validat -
ed cut-off value of CA-125 may be used reliably to stratify the
post-treatment patients or to plan a novel consolidation treat-
ment for the better outcome of the poor prognostic group.
In the future, we expect other biomarkers including HE4
could be used for monitoring the response to therapy and
the course of the disease as CA-125. Further studies should
be performed to provide evidence not only on the diagnostic
value of tumor biomarkers but also their potential prognostic
or predictive value for the management of EOC patients.
CONFLICT OF INTEREST
No potential conflicts of interest relevant to this article were
reported.
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