Diagnostic value of KLK6 as an ovarian cancer biomarker: A meta-analysis.

Biomed Rep

Department of Laboratory Medicine, General Hospital of Ji'nan Military Command Region, Ji'nan, Shandong 250031, P.R. China.

Published: June 2016

AI Article Synopsis

  • * The analysis included five studies with a total of 1,150 participants, showing KLK6 has 91% specificity for ovarian cancer, while its sensitivity stands at 50%.
  • * Combining KLK6 with the existing cancer antigen 125 (CA125) test improves diagnostic accuracy, but more research is needed due to the limited number of studies and samples available.

Article Abstract

Kallikrein-related peptidase 6 (KLK6) is a new potential serum biomarker of ovarian cancer. The aim of the present study was to assess the diagnostic value of KLK6 systematically for ovarian cancer. All the selected studies regarding the changes of KLK6 in ovarian cancer were published prior to April 2015. Five studies involving 485 patients with ovarian cancer, 420 benign cysts and 245 healthy controls met the inclusion criteria. The value of sensitivity, specificity, positive-likelihood ratio (LR+), negative-likelihood ratio (LR-) and area under the receiver operating characteristic curve (ROC) were obtained. All these indices were used to evaluate the diagnostic value of KLK6 for ovarian cancer. The values of sensitivity, specificity, LR+ and LR- (95% confidence interval) of KLK6 were 0.50 (0.47-0.54), 0.91 (0.89-0.93), 7.20 (3.34-15.52) and 0.51 (0.43-0.62), respectively. The area under the summary ROC of KLK6 was 0.86. The index of Q* was 0.79. In conclusion, KLK6 showed high specificity for the diagnosis of ovarian cancer. It can improve the diagnostic accuracy of cancer antigen 125 (CA125). A combined panel of CA125 and KL K6 shows a high diagnostic efficiency for advanced ovarian cancer. Owing to the small number of studies and lack of samples, additional studies meeting the inclusion criteria are required to further analyze the diagnostic value of KLK6 for ovarian cancer.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4887959PMC
http://dx.doi.org/10.3892/br.2016.662DOI Listing

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