Primary treatment approaches in advanced HRD-positive (BRCAm and BRCAwt) ovarian cancer in the Russian non-interventional OVARD study.
e17561 Background: Homologous recombination deficiency (HRD) positive status is a clinically meaningful biomarker in ovarian cancer (OC), associated with improved progression-free survival with the addition of olaparib (ola) to bevacizumab (bev) as maintenance after first-line therapy in PAOLA-1 study. The OVARD study evaluated real-world primary treatment patterns in HRD+BRCAm and HRD+BRCAwt high-grade OC (HGOC). Methods: This non-interventional study analyzed demographics, clinical characteristics, surgery and systemic treatment in HRD+BRCAm and HRD+BRCAwt HGOC using descriptive statistics; multivariable analysis explored factors associated with treatment choice. Results: A total of 400 patients (pts) with newly diagnosed HRD-positive HGOC (FIGO IC–IV) who completed surgery and first-line carboplatin/paclitaxel with or without bev at 29 Russian sites were analyzed: 234 BRCAm and 160 BRCAwt pts. HRD+BRCAm pts were younger (median 52 vs 61 years, p=0.000001) and more frequently had family (44.5% vs 7.5%) and personal (breast cancer 13.3% vs 1.3%) cancer history. HRD status results became available at median 83 days after diagnosis with primary cytoreduction and 105.5 days with interval cytoreduction from routine HRD-testing. Bev was added to first-line chemotherapy in 14.1% (33/234) of BRCAm vs 29.4% (47/160) of BRCAwt pts (p=0.00021), with subsequent ola+bev maintenance in 5.6% vs 17.5% (p=0.00014). Ola maintenance monotherapy was used more often in BRCAm (62.8% vs 35.6%, p=0.000001), while bev monotherapy was more frequent in BRCAwt (14.4% vs 5.1%, p=0.00153). Among pts with residual disease after cytoreduction, response rates to first-line therapy were comparable between BRCAm and BRCAwt (Table). Conclusions: HRD-positive status has become a routine biomarker at HGOC diagnosis and substantially influences first-line and maintenance treatment selection, with bev-containing regimens more often chosen in BRCAwt and ola-based maintenance widely used in both subgroups in real-world practice. Clinical trial information: NCT05918042 . Response on 1 st line therapy in pts with residual disease after cytoreduction. Type of objective response BRCAmn/N BRCAm% BRCAwtn/N BRCAwt% P value Complete response 19/43 44.19 13/36 36.11 0.46653 Partial response 7/43 16.28 10/36 27.78 0.21550
Authors
- H. Musaeva
- V.Kh. Alimov (ORCID: https://orcid.org/0000-0003-4198-8812)
- A. A. Gofman
- И. А. Покатаев (ORCID: https://orcid.org/0000-0001-9864-3837)
- Е. A. Ulrikh (ORCID: https://orcid.org/0000-0002-2701-8812)
- Alexander Valerievich Sultanbaev
- Svetlana Victorovna Khokhlova
- Valeria Saevets
- Natalia Prokudina
- Daniil Stroyakovskiy
- Ruslan Zukov
- Denis Iukalchuk
- Svetlana Goncharova
- Olga Vedrova
- Alexey Rumyantsev
- Orazgul Aymamedova
- Larisa Kolomiets
- Sergey Belonogov
- Yana Chapko
- Rashida Orlova
Institutions
- Russian Academy of Sciences (RU)
- St Petersburg University (RU)
- Federal Almazov North-West Medical Research Centre (RU)
- Moscow Clinical Scientific Center (RU)
- Krasnoyarsk State Medical University (RU)
- Russian Customs Academy (RU)
- Ministry of Health of the Russian Federation (RU)
- Tomsk National Research Medical Center (RU)
- Botkin Hospital (RU)
- Irkutsk Regional Clinical Hospital (RU)
- Republican Oncological Clinical Dispensary (RU)
- Ministry of Health (MN)
- National Medical Research Center for Obstetrics, Gynecology and Perinatology named after Academician V.I.Kulakov of the Ministry of Healthcare of the Russian Federation (RU)
- GOUZ YaO "Solovyov NV Clinical Emergency Hospital" (RU)
- Arkhangel'skiy Klinicheskiy Onkologicheskiy Dispanser (RU)
- National Medical Research Center of Cardiology (RU)
- State Healthcare Institution "Regional Clinical Oncological Dispensary" (RU)
- Chelyabinsk Regional Clinical Oncology Center (RU)
- Moscow City Oncology Hospital №62 (RU)
- Kaliningrad State Technical University (RU)
Publication Details
- Journal
- Journal of Clinical Oncology
- Published
- 2026-05-28
- DOI
- https://doi.org/10.1200/jco.2026.44.16_suppl.e17561
- Primary Topic
- PARP inhibition in cancer therapy
- Type
- article
- Field-Weighted Citation Impact
- 0.00