Abstract:
:Although 70-80% of newly diagnosed ovarian cancer patients respond to first-line therapy, almost all relapse and five-year survival remains below 50%. One strategy to increase five-year survival is prolonging time to relapse by improving first-line therapy response. However, no biomarker today can accurately predict individual response to therapy. In this study, we present analytical and prospective clinical validation of a new test that utilizes primary patient tissue in 3D cell culture to make patient-specific response predictions prior to initiation of treatment in the clinic. Test results were generated within seven days of tissue receipt from newly diagnosed ovarian cancer patients obtained at standard surgical debulking or laparoscopic biopsy. Patients were followed for clinical response to chemotherapy. In a study population of 44, the 32 test-predicted Responders had a clinical response rate of 100% across both adjuvant and neoadjuvant treated populations with an overall prediction accuracy of 89% (39 of 44, p < 0.0001). The test also functioned as a prognostic readout with test-predicted Responders having a significantly increased progression-free survival compared to test-predicted Non-Responders, p = 0.01. This correlative accuracy establishes the test's potential to benefit ovarian cancer patients through accurate prediction of patient-specific response before treatment.
journal_name
Sci Repjournal_title
Scientific reportsauthors
Shuford S,Wilhelm C,Rayner M,Elrod A,Millard M,Mattingly C,Lotstein A,Smith AM,Guo QJ,O'Donnell L,Elder J,Puls L,Weroha SJ,Hou X,Zanfagnin V,Nick A,Stany MP,Maxwell GL,Conrads T,Sood AK,Orr D,Holmes LM,Gevaertdoi
10.1038/s41598-019-47578-7subject
Has Abstractpub_date
2019-08-01 00:00:00pages
11153issue
1issn
2045-2322pii
10.1038/s41598-019-47578-7journal_volume
9pub_type
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