ChemoID-guided therapy improves objective response rate in recurrent platinum-resistant ovarian cancer randomized clinical trial

Patients with recurrent platinum-resistant ovarian cancer (PROC) have poor clinical outcomes, owing mainly to the presence of therapy-resistant cancer stem cells (CSCs). The NCT03949283 randomized clinical trial enrolled patients with recurrent PROC to receive ChemoID-guided chemotherapy or the best physician-choice regimen selected from the same list of thirteen mono or combination chemotherapies. The primary outcome was objective response rate (ORR) assessed on CT scans using the RECIST 1.1 criteria at 6 months follow-up. Subjects treated with the ChemoID assay had an ORR of 55% (CI<sub>95</sub> 39% - 73%), compared to 5% (CI<sub>95</sub> 0% - 11%) for those treated with physician's choice chemotherapy (p <0.0001). Secondary endpoints of duration of response (DOR) and progression-free survival (PFS) of subjects treated with chemotherapies guided by the ChemoID assay versus physician's choice chemotherapy were a median of 8 months vs. 5.5 months (p <0.0001), and 11.0 months (CI<sub>95</sub> 8.0- NA) vs 3.0 months (CI<sub>95</sub> 2.0- 3.5) with 27% of hazard ratio (CI95, 0.15-0.49; p <0.001), respectively.

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Publication Details

Journal
npj Precision Oncology
Published
2025-03-25
DOI
https://doi.org/10.1038/s41698-025-00874-0
Citations
2
Primary Topic
Ovarian cancer diagnosis and treatment
Type
article
Field-Weighted Citation Impact
3.40
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article

ChemoID-guided therapy improves objective response rate in recurrent platinum-resistant ovarian cancer randomized clinical trial

Thomas C. Krivak, John P. Diaz, Pier Paolo Claudio, Abhijit Barve et al.
2 citations
npj Precision Oncology
Ovarian cancer diagnosis and treatment
3.40
article

ChemoID-guided therapy improves objective response rate in recurrent platinum-resistant ovarian cancer randomized clinical trial

Thomas C. Krivak, John P. Diaz, Pier Paolo Claudio, Abhijit Barve, Scott E. Lentz, Candace M. Howard, Stephen Bush, Nadim Bou Zgheib, Jagan Valluri, Navya Nair, Krista L. Denning, Camille Gunderson-Jackson, Seth T. Lirette, Thomas J. Herzog
article en
2 citations

Abstract

Patients with recurrent platinum-resistant ovarian cancer (PROC) have poor clinical outcomes, owing mainly to the presence of therapy-resistant cancer stem cells (CSCs). The NCT03949283 randomized clinical trial enrolled patients with recurrent PROC to receive ChemoID-guided chemotherapy or the best physician-choice regimen selected from the same list of thirteen mono or combination chemotherapies. The primary outcome was objective response rate (ORR) assessed on CT scans using the RECIST 1.1 criteria at 6 months follow-up. Subjects treated with the ChemoID assay had an ORR of 55% (CI<sub>95</sub> 39% - 73%), compared to 5% (CI<sub>95</sub> 0% - 11%) for those treated with physician's choice chemotherapy (p <0.0001). Secondary endpoints of duration of response (DOR) and progression-free survival (PFS) of subjects treated with chemotherapies guided by the ChemoID assay versus physician's choice chemotherapy were a median of 8 months vs. 5.5 months (p <0.0001), and 11.0 months (CI<sub>95</sub> 8.0- NA) vs 3.0 months (CI<sub>95</sub> 2.0- 3.5) with 27% of hazard ratio (CI95, 0.15-0.49; p <0.001), respectively.

npj Precision OncologyVol. 9(1)
Louisiana State University (US), Baptist Hospital of Miami (US), Allegheny Health Network (US), Charleston Area Medical Center (US), Kaiser Permanente (US), University of Miami (US), Huntington University (US), Jackson Memorial Hospital (US), University of Mississippi Medical Center (US), Mercy Clinic Neurology (US), Los Angeles Medical Center (US), Baptist Health South Florida (US), Psychogenics (United States) (US), Edwards Comprehensive Cancer Center (US), Sylvester Comprehensive Cancer Center (US), Tris Pharma (United States) (US), University of Oklahoma Health Sciences Center (US), University of Cincinnati (US), Marshall University (US)
Good health and well-being
Openalex Percentile: Top 9%
Ovarian cancer diagnosis and treatment
3.40
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