Comparison of Different Maintenance Treatment Options for Newly Diagnosed <i>BRCA</i> wt Advanced Ovarian Cancer: A Retrospective Cohort Analysis

IntroductionNiraparib and bevacizumab are two principal maintenance therapies for newly diagnosed advanced ovarian cancer (AOC) patients with <i>BRCA</i> wild-type (<i>BRCA</i>wt) status, regardless of homologous recombination deficiency (HRD). In China, however, a considerable proportion of <i>BRCA</i>wt patients have unknown or untested HRD status, complicating treatment selection.MethodsTo evaluate and compare the efficacy of niraparib and bevacizumab as maintenance therapy for <i>BRCA</i>wt AOC, we conducted a retrospective cohort study using real-world clinical data. Descriptive statistics were used to summarize clinical and demographic characteristics. Progression-free survival (PFS) was estimated using Kaplan-Meier analysis and compared using a stratified Cox proportional hazards model. A multivariable Cox regression was performed to adjust for potential confounding variables. Exploratory subgroup analyses were conducted, and propensity score matching (PSM) was applied as a sensitivity analysis.ResultsA total of 94 patients were included, with 51 receiving niraparib and 43 receiving bevacizumab. The median PFS was not reached in the niraparib group versus 13.77 months (95% CI, 4.12-23.41) in the bevacizumab group (HR = 0.240, 95% CI, 0.128-0.451; <i>P</i> < .001). After covariate adjustment, the median PFS was 19.55 months (95% CI, 9.40-NA) with niraparib and 8.64 months (95% CI, 4.53-NA) with bevacizumab, with an adjusted HR of 0.282 (95% CI, 0.136-0.587; <i>P</i> = .001). In the PSM sensitivity analysis, the median PFS was not reached (95% CI, 19.55-NR) in the niraparib group and was 18.33 months (95% CI, 8.90-25.26) in the bevacizumab group (HR = 0.360, 95% CI, 0.176-0.736; <i>P</i> = .005).ConclusionThis analysis suggests that niraparib may provide a progression-free survival advantage compared with bevacizumab in <i>BRCA</i>wt AOC patients, with both regimens appearing to be generally well tolerated in the real-world setting. These findings offer preliminary reference value for maintenance treatment selection in patients with newly diagnosed <i>BRCA</i>wt AOC.

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Journal
Technology in Cancer Research & Treatment
Published
2026-02-01
DOI
https://doi.org/10.1177/15330338261416162
Primary Topic
PARP inhibition in cancer therapy
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article
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article

Comparison of Different Maintenance Treatment Options for Newly Diagnosed BRCA wt Advanced Ovarian Cancer: A Retrospective Cohort Analysis

Y. Zhang, Chenyan FANG, Yanglong Guo, Xi Chen
Technology in Cancer Research & Treatment
PARP inhibition in cancer therapy
article

Comparison of Different Maintenance Treatment Options for Newly Diagnosed BRCA wt Advanced Ovarian Cancer: A Retrospective Cohort Analysis

Y. Zhang, Chenyan FANG, Yanglong Guo, Xi Chen
article en

Abstract

IntroductionNiraparib and bevacizumab are two principal maintenance therapies for newly diagnosed advanced ovarian cancer (AOC) patients with <i>BRCA</i> wild-type (<i>BRCA</i>wt) status, regardless of homologous recombination deficiency (HRD). In China, however, a considerable proportion of <i>BRCA</i>wt patients have unknown or untested HRD status, complicating treatment selection.MethodsTo evaluate and compare the efficacy of niraparib and bevacizumab as maintenance therapy for <i>BRCA</i>wt AOC, we conducted a retrospective cohort study using real-world clinical data. Descriptive statistics were used to summarize clinical and demographic characteristics. Progression-free survival (PFS) was estimated using Kaplan-Meier analysis and compared using a stratified Cox proportional hazards model. A multivariable Cox regression was performed to adjust for potential confounding variables. Exploratory subgroup analyses were conducted, and propensity score matching (PSM) was applied as a sensitivity analysis.ResultsA total of 94 patients were included, with 51 receiving niraparib and 43 receiving bevacizumab. The median PFS was not reached in the niraparib group versus 13.77 months (95% CI, 4.12-23.41) in the bevacizumab group (HR = 0.240, 95% CI, 0.128-0.451; <i>P</i> < .001). After covariate adjustment, the median PFS was 19.55 months (95% CI, 9.40-NA) with niraparib and 8.64 months (95% CI, 4.53-NA) with bevacizumab, with an adjusted HR of 0.282 (95% CI, 0.136-0.587; <i>P</i> = .001). In the PSM sensitivity analysis, the median PFS was not reached (95% CI, 19.55-NR) in the niraparib group and was 18.33 months (95% CI, 8.90-25.26) in the bevacizumab group (HR = 0.360, 95% CI, 0.176-0.736; <i>P</i> = .005).ConclusionThis analysis suggests that niraparib may provide a progression-free survival advantage compared with bevacizumab in <i>BRCA</i>wt AOC patients, with both regimens appearing to be generally well tolerated in the real-world setting. These findings offer preliminary reference value for maintenance treatment selection in patients with newly diagnosed <i>BRCA</i>wt AOC.

Technology in Cancer Research & TreatmentVol. 25
Wenzhou Medical University (CN), Zhejiang Cancer Hospital (CN), Cancer Hospital of Chinese Academy of Medical Sciences (CN), University of Chinese Academy of Sciences (CN)
Good health and well-being
Openalex Percentile: Top 66%
PARP inhibition in cancer therapy
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