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open access
Published: 25 April 2013
Abstract (provisional)
Purpose: The capacity of nadir CA-125 levels to predict the prognosis of epithelial
ovarian cancer remains controversial. This study aimed to explore whether the nadir
CA-125 serum levels could predict the durations of overall survival (OS) and progression
free survival (PFS) in patients with high-grade serous ovarian cancer (HG-SOC) from
the USA and PRC.
Materials and methods: A total of 616 HG-SOC patients from the MD Anderson Cancer
Center (MDACC, USA) between 1990 and 2011 were retrospectively analyzed. The results
of 262 cases from the Jiangsu Institute of Cancer Research (JICR, PRC) between 1992
and 2011 were used to validate the MDACC data. The CA-125 immunohistochemistry assay
was performed on 280 tissue specimens. The Cox proportional hazards model and the
log-rank test were used to assess the associations between the clinicopathological
characteristics and duration of survival.
Results
The nadir CA-125 level was an independent predictor of OS and PFS (p < 0.01 for both)
in the MDACC patients. Lower nadir CA-125 levels (<=10 U/mL) were associated with
longer OS and PFS (median: 61.2 and 16.8 months with 95% CI: 52.0--72.4 and 14.0--19.6
months, respectively) than their counterparts with shorter OS and PFS (median: 49.2
and 10.5 months with 95% CI: 41.7--56.7 and 6.9--14.1 months, respectively). The nadir
CA-125 levels in JICR patients were similarly independent when predicting the OS and
PFS (p < 0.01 for both). Nadir CA-125 levels less than or equal to 10 U/mL were associated
with longer OS and PFS (median: 59.9 and 15.5 months with 95% CI: 49.7--70.1 and 10.6--20.4
months, respectively), as compared with those more than 10 U/mL (median: 42.0 and
9.0 months with 95% CI: 34.4--49.7 and 6.6--11.2 months, respectively). Baseline serum
CA-125 levels, but not the CA-125 expression in tissues, were associated with the
OS and PFS of HG-SOC patients in the MDACC and JICR groups. However, these values
were not independent. Nadir CA-125 levels were not associated with the tumor burden
based on second-look surgery (p = 0.09). Patients who achieved a pathologic complete
response had longer OS and PFS (median: 73.7 and 20.7 months with 95% CI: 63.7--83.7
and 9.5--31.9 months, respectively) than those with residual tumors (median: 34.6
and 10.6 months with 95% CI: 6.9--62.3 and 4.9--16.3 months, respectively).
Conclusions
The nadir CA-125 level was an independent predictor of OS and PFS in HG-SOC patients.
Further prospective studies are required to clinically optimize the chances for a
complete clinical response of HG-SOC cases with higher CA-125 levels (>10 U/mL) at
the end of primary treatment.
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