Study protocol for Adaptive ChemoTherapy for Ovarian cancer (ACTOv): a multicentre phase II randomised controlled trial to evaluate the efficacy of adaptive therapy (AT) with carboplatin, based on changes in CA125, in patients with relapsed platinum-sensitive high-grade serous or high-grade endometrioid ovarian cancer

Study Overview: ACTOv Trial

Title: Adaptive ChemoTherapy for Ovarian Cancer (ACTOv)

This is a phase II study to test a new way of treating ovarian cancer using a drug called carboplatin. It focuses on women whose cancer has returned after treatment and is still sensitive to platinum-based therapies.

What is Adaptive Therapy?

Adaptive therapy (AT) is a fresh approach that adjusts drug doses based on how well patients respond to treatment. The goal is to balance the fight between sensitive and resistant cancer cells, potentially improving outcomes.

Study Details

  • Participants: 80 women with relapsed high-grade ovarian cancer.
  • Groups: Randomly assigned to either standard treatment or adaptive therapy.
  • Treatment Schedule: Carboplatin administered intravenously every 21 days, up to 6 cycles for standard treatment and 12 cycles for adaptive therapy.
  • Key Measurement: Progression-free survival and other health outcomes.

Ethics and Sharing Results

The study has ethical approval and results will be shared in scientific journals to inform the medical community.

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