Efficacy of subsequent therapies in patients with advanced ovarian cancer who relapse after first-line olaparib maintenance: results of the PAOLA-1/ENGOT-ov25 trial

  • 0Department of Gynaecology & Gynaecologic Oncology, Ev. Kliniken Essen-Mitte, Essen, Germany; Philipps University, Marburg, Germany; Arbeitsgemeinschaft Gynäkologische Onkologie (AGO) Studiengruppe, Germany.

Summary

This summary is machine-generated.

First-line poly(ADP-ribose) polymerase inhibitor maintenance therapy is rising for ovarian cancer. Progression timing after first-line olaparib maintenance impacts subsequent therapy efficacy, with longer duration when progression occurs after treatment completion.

Area Of Science

  • Oncology
  • Gynecologic Oncology
  • Clinical Pharmacology

Background

  • Increasing use of first-line poly(ADP-ribose) polymerase (PARP) inhibitor maintenance therapy in advanced ovarian cancer.
  • Need to understand first subsequent therapy (FST) efficacy after disease progression in the first-line setting.
  • Evaluation of FST efficacy in patients from the PAOLA-1/ENGOT-ov25 trial who received first-line olaparib maintenance.

Purpose Of The Study

  • To evaluate the efficacy of FST in advanced ovarian cancer patients who received first-line olaparib maintenance.
  • To assess the impact of disease progression timing (during vs. after first-line olaparib maintenance) on FST efficacy.
  • To identify prognostic factors for subsequent chemotherapy efficacy in the olaparib plus bevacizumab arm.

Main Methods

  • Post hoc analysis of the PAOLA-1/ENGOT-ov25 trial.
  • Assessment of time from FST to second subsequent therapy (SST).
  • Multivariate Cox model analysis in the olaparib plus bevacizumab arm to identify prognostic factors.

Main Results

  • Of 806 patients, 544 (67.5%) progressed and received subsequent chemotherapy.
  • Median time from FST to SST was shorter (6.1 months) for progression during first-line olaparib maintenance versus after (11.4 months).
  • Progression after first-line olaparib maintenance was an independent prognostic factor for longer time from FST to SST (HR 0.65, P=0.0011).

Conclusions

  • Timing of disease progression relative to first-line olaparib maintenance influences subsequent platinum-based chemotherapy efficacy.
  • Longer time from FST to SST observed when progression occurs after first-line olaparib maintenance compared to during.
  • Efficacy of subsequent therapies, including PARP inhibitor rechallenge, is dependent on progression timing.

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