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September 23, 2025Cancer Medicine1 citationsOpen Access

Sensitivity of Platinum‐Based Chemotherapy and Efficacy of Arsenic Trioxide‐Based Non‐Platinum Chemotherapy Following the Progression of PARPi Maintenance Therapy: A Real‐World Study

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RGRui GouQXQi XieHRHua Ren

Key Points

  • Overall response rate for arsenic trioxide-based chemotherapy was 57.1%, indicating its potential effectiveness.
  • Patients receiving PARPi for more than 12 months showed a significantly shorter time to second progression at 3.45 months.
  • Out of 41 patients, 34 received platinum-based chemotherapy with an overall response rate of 26.5%, showing limited efficacy.
  • Non-platinum sequential chemotherapy may present a preferable strategy for managing PARPi resistance in patients.

Abstract

ABSTRACT Background Cross‐resistance is observed between platinum and Poly (ADP‐ribose) polymerase inhibitors (PARPi). We aim to propose the definition of PARPi resistance and demonstrate the best therapeutic strategy for patients with PARPi resistance. Methods A retrospective analysis was performed on patients diagnosed with epithelial ovarian cancer from October 2015 to November 2022. Patients were treated with PARPi for more than 6 months and received chemotherapy after progression. Results Totally, 41 patients were enrolled, with 21 receiving PARPi for 6 to 12 months and 20 for more than 12 months. The median duration of PARPi was 12 months, and the median time to second progression (TTSP) was 3.45 months (range, 1.0–20.2 months). The Kaplan–Meier and Cox analysis revealed a significantly shorter TTSP for patients who received PARPi for more than 12 months compared to those for 6 to 12 months. After PARPi resistance, 34 (82.9%) received platinum‐based chemotherapy, with an overall response rate (ORR) of 26.5% (9/34). Seven patients (17.1%) received arsenic trioxide (ATO)‐based chemotherapy, with an ORR of 57.1% (4/7). During subsequent chemotherapy, 12/34 patients switched to ATO‐based chemotherapy due to progression, of which five cases were evaluated as effective (41.7%). Conclusion PARPi resistance has a negative impact on the subsequent chemotherapy. The progression of the disease beyond 6 to 12 months should be considered as acquired resistance. Non‐platinum chemotherapy, such as ATO‐based combined sequential chemotherapy, may emerge as the preferred option for patients with PARPi resistance.

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Cite This Study

Gou et al. (2025) studied this question.

synapsesocial.com/papers/68d473ad31b076d99fa6c4bchttps://doi.org/10.1002/cam4.71208
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