O025/#522 Maintenance olaparib rechallenge in patients with ovarian cancer previously treated with a parp inhibitor: patient-reported outcomes from the phase IIIB OReO/engot-ov38 trial. (4th December 2022)
- Record Type:
- Journal Article
- Title:
- O025/#522 Maintenance olaparib rechallenge in patients with ovarian cancer previously treated with a parp inhibitor: patient-reported outcomes from the phase IIIB OReO/engot-ov38 trial. (4th December 2022)
- Main Title:
- O025/#522 Maintenance olaparib rechallenge in patients with ovarian cancer previously treated with a parp inhibitor: patient-reported outcomes from the phase IIIB OReO/engot-ov38 trial
- Authors:
- Redondo, Andrés
Follana, Philippe
Scambia, Giovanni
Asselain, Bernard
Marmé, Frederik
Mirza, Mansoor
Laudani, Maria Elena
Mądry, Radosław
Glasspool, Rosalind
You, Benoit
Rubio-Perez, María Jesús
Zamagni, Claudio
El-Balat, Ahmed
Hardy-Bessard, Anne Claire
Oaknin, Ana
Ronzino, Graziana
Shaw, Bob
Nakamura, Hitomi
Berton, Dominique
Pujade-Lauraine, Eric - Abstract:
- Abstract : Objectives: In OReO/ENGOT-ov38 (NCT03106987 ), maintenance olaparib rechallenge significantly improved progression-free survival (PFS) versus placebo in platinumsensitive relapsed ovarian cancer (PSROC), irrespective of BRCA1/BRCA2 mutation (BRCAm) status (BRCAm: hazard ratio [HR] 0.57, 95% confidence interval [CI] 0.37–0.87; P=0.022; non-BRCAm: HR 0.43, 95% CI 0.26–0.71; P=0.002) (PujadeLauraine et al. ESMO 2021). We assessed health-related quality of life (HRQoL) by patient-reported outcomes (PROs). Methods: Patients with PSROC, prior PARP inhibitor maintenance (one line), and in response to last platinum-based chemotherapy were randomized (BRCAm and non-BRCAm cohorts) to maintenance olaparib (300 mg bid) or placebo until progression. Prespecified secondary PROs included change from baseline in Functional Assessment of Cancer Therapy-Ovarian (FACT-O) Trial Outcome Index (TOI), and best response and improvement in TOI. The minimally important difference (MID) for clinically meaningful change in TOI was 10 points. Results: Patients were randomized in cohorts (BRCAm: olaparib=74, placebo=38; non-BRCAm: olaparib=72, placebo=36). The difference between olaparib and placebo in the overall adjusted mean change in TOI score was not considered clinically meaningful in either cohort as 95% CIs lay within the MID interval: BRCAm, -2.94 (95% CI -4.99 to -0.90); non-BRCAm, -2.66 (95% CI -4.75 to -0.58) ( figure 1 ). Most olaparib and placebo patients had a best response ofAbstract : Objectives: In OReO/ENGOT-ov38 (NCT03106987 ), maintenance olaparib rechallenge significantly improved progression-free survival (PFS) versus placebo in platinumsensitive relapsed ovarian cancer (PSROC), irrespective of BRCA1/BRCA2 mutation (BRCAm) status (BRCAm: hazard ratio [HR] 0.57, 95% confidence interval [CI] 0.37–0.87; P=0.022; non-BRCAm: HR 0.43, 95% CI 0.26–0.71; P=0.002) (PujadeLauraine et al. ESMO 2021). We assessed health-related quality of life (HRQoL) by patient-reported outcomes (PROs). Methods: Patients with PSROC, prior PARP inhibitor maintenance (one line), and in response to last platinum-based chemotherapy were randomized (BRCAm and non-BRCAm cohorts) to maintenance olaparib (300 mg bid) or placebo until progression. Prespecified secondary PROs included change from baseline in Functional Assessment of Cancer Therapy-Ovarian (FACT-O) Trial Outcome Index (TOI), and best response and improvement in TOI. The minimally important difference (MID) for clinically meaningful change in TOI was 10 points. Results: Patients were randomized in cohorts (BRCAm: olaparib=74, placebo=38; non-BRCAm: olaparib=72, placebo=36). The difference between olaparib and placebo in the overall adjusted mean change in TOI score was not considered clinically meaningful in either cohort as 95% CIs lay within the MID interval: BRCAm, -2.94 (95% CI -4.99 to -0.90); non-BRCAm, -2.66 (95% CI -4.75 to -0.58) ( figure 1 ). Most olaparib and placebo patients had a best response of no change in TOI; no significant differences in proportion with improvement in TOI were observed ( table 1 ). Few olaparib and placebo patients had a TOI deterioration: BRCAm, 10 (14%) and 4 (11%); non-BRCAm, 10 (15%) and 2 (6%). Conclusions: Maintenance olaparib rechallenge significantly improved PFS over placebo, without clinically meaningful change in HRQoL. Clinical trial ID: NCT03106987 … (more)
- Is Part Of:
- International journal of gynecological cancer. Volume 32(2022)Supplement 3
- Journal:
- International journal of gynecological cancer
- Issue:
- Volume 32(2022)Supplement 3
- Issue Display:
- Volume 32, Issue 3 (2022)
- Year:
- 2022
- Volume:
- 32
- Issue:
- 3
- Issue Sort Value:
- 2022-0032-0003-0000
- Page Start:
- A15
- Page End:
- A15
- Publication Date:
- 2022-12-04
- Subjects:
- Generative organs, Female -- Cancer -- Periodicals
616.99465 - Journal URLs:
- http://journals.lww.com/ijgc/pages/default.aspx ↗
http://www3.interscience.wiley.com/journal/118544021/toc ↗
https://ijgc.bmj.com/ ↗
http://journals.lww.com ↗ - DOI:
- 10.1136/ijgc-2022-igcs.27 ↗
- Languages:
- English
- ISSNs:
- 1048-891X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4542.273500
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 24964.xml