Clinical and biomarker factors affecting survival in patients with platinum-sensitive relapsed ovarian cancer receiving olaparib monotherapy: a multicenter retrospective study
The standard treatment for platinum-sensitive relapsed ovarian cancer (PSROC) is platinum-based chemotherapy followed by olaparib monotherapy. A retrospective study was conducted to identify factors affecting the survival of patients with PSROC undergoing olaparib monotherapy in real-world clinical...
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Veröffentlicht in: | Scientific reports 2023-07, Vol.13 (1), p.11962-11962, Article 11962 |
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Sprache: | eng |
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Zusammenfassung: | The standard treatment for platinum-sensitive relapsed ovarian cancer (PSROC) is platinum-based chemotherapy followed by olaparib monotherapy. A retrospective study was conducted to identify factors affecting the survival of patients with PSROC undergoing olaparib monotherapy in real-world clinical settings. The study enrolled 122 patients who received olaparib monotherapy between April 2018 and December 2020 at three national centers in Japan. The study used the Kaplan–Meier method and univariable and multivariable Cox proportional hazards models to evaluate the associations between factors and progression-free survival (PFS). Patients with
BRCA1/2
mutations had a significantly longer median PFS than those without these mutations. Both the
BRCA1/2
mutation-positive and mutation-negative groups exhibited a prolonged PFS when the platinum-free interval (PFI) was ≥ 12 months. Cancer antigen 125 (CA-125) level within reference values was significantly linked to prolonged PFS, while a high platelet-to-lymphocyte ratio (≥ 210) was significantly associated with poor PFS in the
BRCA1/2
mutation-negative group. The study suggests that a PFI of ≥ 12 months may predict survival after olaparib monotherapy in patients with PSROC, regardless of their
BRCA1/2
mutation status. Additionally, a CA-125 level within reference values may be associated with extended survival in patients without
BRCA1/2
mutations. A larger prospective study should confirm these findings. |
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ISSN: | 2045-2322 2045-2322 |
DOI: | 10.1038/s41598-023-39224-0 |