# Predicting platinum-resistance in advanced ovarian cancer: defining patient and disease characteristics to improve treatment approaches at initiation of treatment or earlier in the course of the disease

**Authors:** Dana M. Chase, Gregory Patton, Srinivas Annavarapu, Junxin Shi, Elizabeth Szamreta, Matthew Monberg

PMC · DOI: 10.3389/fonc.2026.1765220 · Frontiers in Oncology · 2026-02-13

## TL;DR

This study identifies patient and disease characteristics linked to platinum resistance in advanced ovarian cancer, aiming to improve treatment strategies at diagnosis.

## Contribution

The study identifies clinical factors associated with platinum resistance in ovarian cancer patients in a real-world community oncology setting.

## Key findings

- Stage IV disease was significantly associated with platinum resistance compared to Stage III.
- Platinum-resistant patients had poorer survival outcomes and shorter progression-free survival.
- Obesity and ECOG 2+ were non-significantly associated with higher odds of platinum resistance.

## Abstract

This study aimed to describe differences in characteristics and outcomes between patients with platinum sensitive or platinum resistant advanced ovarian cancer in a community oncology setting.

This was a retrospective study of adult patients with Stage III/IV ovarian cancer who received 4+ cycles of a front-line platinum-based regimen between 01/01/2017 and 06/30/2021 (followed until 12/31/2021) within The US Oncology Network. Platinum sensitive or resistant patients were included while refractory patients were excluded. Structured and chart review data were used. Multivariable logistic regression assessed factors associated with platinum sensitivity vs. resistance.

A total of 108 platinum sensitive and 34 resistant patient charts were reviewed. In addition to platinum-based chemotherapy, 19% of patients also initiated bevacizumab as part of their front-line regimen. Most patients were White (63%) and diagnosed at Stage IIIC (55%) or IV (33%). ECOG performance status scores were 0/1 for 47% and 2+ for 20% of patients while BRCA mutations were observed among 7.7%. Sensitive vs. resistant patients were younger (p=0.045) and fewer were obese (p=0.011). Stage IV disease (odds ratio [OR]=3.6, p=0.009) was associated with significantly higher odds of platinum resistance after front-line treatment compared to Stage III, while obesity (OR = 2.6, p=0.067) and ECOG 2+ (OR = 2.9, p=0.057) were non-significantly associated with higher odds of resistance. Median overall survival was not reached in sensitive patients, and was 16.7 months in resistant patients. Median progression-free survival in sensitive and resistant patients was 19.6 and 7.9 months, respectively.

When exploring factors associated with response to front-line platinum-based treatment of ovarian cancer, Stage IV disease was significantly associated with resistance. As platinum resistant patients have poorer survival and fewer treatment options, it is important to further define the biology and appropriate initial management of these patients.

## Linked entities

- **Genes:** Brca2 (BRCA2, DNA repair associated) [NCBI Gene 37916]
- **Diseases:** ovarian cancer (MONDO:0005140)

## Full-text entities

- **Genes:** BRCA1 (BRCA1 DNA repair associated) [NCBI Gene 672] {aka BRCAI, BRCC1, BROVCA1, FANCS, IRIS, PNCA4}, MUC16 (mucin 16, cell surface associated) [NCBI Gene 94025] {aka CA125}
- **Diseases:** (stage III/IV) (MESH:D062706), International (MESH:D000082122), PR (MESH:D008151), Breast Cancer (MESH:D001943), Obesity (MESH:D009765), IV disease (MESH:D020432), overweight (MESH:D050177), epithelial ovarian cancer (MESH:D000077216), Stage III/IV ovarian cancer (MESH:D010051), myocardial infarction (MESH:D009203), Stage IV disease (MESH:D007676), cancer (MESH:D009369), advanced (MESH:D020178), Obstetrics Stage II-IV) (MESH:D048949), CCI (MESH:C566784), inflammatory (MESH:D007249), metastases (MESH:D009362), Death (MESH:D003643)
- **Chemicals:** Bevacizumab (MESH:D000068258), liposomal doxorubicin (MESH:C506643), olaparib (MESH:C531550), pembrolizumab (MESH:C582435), paclitaxel (MESH:D017239), 1L (-), Platinum (MESH:D010984), pemetrexed (MESH:D000068437), doxorubicin (MESH:D004317), letrozole (MESH:D000077289), deoxyribose (MESH:D003855), carboplatin (MESH:D016190)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

31 references — full list in the complete paper: https://tomesphere.com/paper/PMC12946934/full.md

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Source: https://tomesphere.com/paper/PMC12946934