Impact of disease progression on health-related quality of life (HRQOL): Updated results from the PRIMA/ENGOT-OV26/GOG-3012 trial of niraparib first-line (1L) maintenance therapy in patients with newly diagnosed advanced ovarian cancer (aOC).

M Mark S. Shahin (PennState Health, Hershey) M Maria-Pilar Barretina-Ginesta (Grupo Español de Investigación en Cáncer de Ovario (GEICO) and Medical Oncology Department, Institut Català d´Oncologia (ICO), Girona, Spain) D David M. O’Malley (The Ohio State University and the James Comprehensive Cancer Center, Columbus, OH) B Brigitte Honhon (Grand Hôpital de Charleroi, Charleroi, Belgium) C Colleen C. McCormick (Legacy Medical Group Gynecologic Oncology, Portland, OR) S Sakari Hietanen (Turku University Hospital and NSGO-CTU, Turku, Finland) R Roisin E. O’Cearbhaill (Memorial Sloan Kettering Cancer Center and Weill Cornell Medical College, New York, NY) G Giorgia Mangili (Department of Obstetrics and Gynecology, San Raffaele Hospital, Milan, Italy) R Richard G. Moore (Division of Gynecologic Oncology, Wilmot Cancer Institute, Department of Obstetrics and Gynecology, University of Rochester, Rochester, NY) D Dominique Berton (Institut de Cancerologie de l'Ouest, Saint-Herblain, France) R Robert Allen Burger (Mersana Therapeutics, a Wholly Owned Subsidiary of Day One Biopharmaceuticals, Cambridge, MA) E Elena Ioana Braicu (Department of Gynecology, Campus Virchow, Charité Universitätsmedizin Berlin and North Eastern German Society for Gynecologic Oncology (NOGGO), Berlin, Germany) B Bradley J. Monk M Maria Jesús Rubio-Pérez (Hospital Universitario Reina Sofia and GEICO, Córdoba, Spain) N Noelle Cloven (Texas Oncology, Fort Worth, Fort Worth, TX) C Charlotte Aaquist Haslund (NSGO-CTU and Aalborg University Hospital, Aalborg, Denmark) T Thomas J Herzog (University of Cincinnati Cancer Center; Department of Obstetrics & Gynecology, College of Medicine, Cincinnati, OH) L Luda Shtessel (GSK, Durham, NC) J Jonathan Lim (The University of Manchester & The Christie NHS Foundation Trust, Manchester, United Kingdom) A Antonio Gonzalez Martin (Grupo Español de Investigación en Cáncer de Ovario (GEICO) and Medical Oncology Department, Clínica Universidad de Navarra, Madrid, Spain)

Abstract

5551 Background: The phase 3 PRIMA trial (NCT02655016) demonstrated that niraparib 1L maintenance therapy significantly extended progression-free survival (PFS) compared with placebo in patients with newly diagnosed aOC that responded to 1L platinum-based chemotherapy. Using data from the Nov 2019 cutoff (median follow-up, ≈1.7 y), pooled results from both treatment arms found that disease progression negatively affected HRQOL. Here we report updated HRQOL results from the PRIMA final analysis. Methods: In PRIMA, patients were randomized 2:1 to niraparib or placebo 1L maintenance once daily. HRQOL was assessed as a prespecified secondary endpoint using patient-reported responses to multiple instruments, including the European Organisation for Research and Treatment of Cancer QOL Core Questionnaire (EORTC QLQ-C30) and the EORTC QLQ Ovarian Cancer Module (EORTC QLQ-OV28). Assessments were collected at baseline, at designated intervals while on study treatment; at the end of treatment (EOT); and at 4, 8, 12, and 24 weeks after the last dose of study treatment. Post hoc analysis results are reported herein (clinical cutoff: Apr 8, 2024; median follow-up, 6.2 y). Results: In the overall population (niraparib, n=487; placebo, n=246), EOT survey completion rates exceeded 80% across both instruments. In both treatment arms, disease progression significantly reduced overall HRQOL per the EORTC QLQ-C30, with marked decreases from the last on-treatment visit (LOTV) for global health status/QOL that never recovered to LOTV levels (Table). Disease progression was also associated with deterioration across all 5 functional scales of the EORTC QLQ-C30 and worsening symptoms of fatigue, nausea/vomiting, pain, dyspnea, appetite loss, diarrhea, and financial difficulties. On the EORTC QLQ-OV28, progression was associated with decreased scores for body image, sexuality, and attitude toward disease/treatment functional scales and worsening abdominal/gastrointestinal symptoms. Conclusions: Disease progression negatively impacted HRQOL across treatment arms in PRIMA. These results support PFS as a clinically relevant endpoint in patients with aOC, as delays in disease progression help preserve HRQOL. Clinical trial information: NCT02655016 . LS mean change from LOTV (95% CI) Niraparib(n=487) Placebo(n=246) EORTC QLQ-C30 global health status/QOL EOT –8.6 (–10.9, –6.4) –7.4 (–10.1, –4.7) Week 4 post EOT –10.0 (–12.7, –7.3) –10.7 (–14.0, –7.4) Week 8 post EOT –10.1 (–12.9, –7.2) –12.2 (–16.0, –8.5) Week 12 post EOT –11.5 (–14.0, –9.1) –9.5 (–12.6, –6.3) Week 24 post EOT –10.7 (–13.4, –8.1) –9.6 (–13.1, –6.2) EORTC QLQ-C30, European Organisation for Research and Treatment of Cancer QOL Core Questionnaire; EOT, end of treatment; LOTV, last on-treatment visit; LS, least squares; QOL, quality of life.

Article Details

Volume / Issue Vol. 43, Issue 16_suppl
Published June 01, 2025
Pages 5551-5551
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (20)

M

Mark S. Shahin

PennState Health, Hershey

M

Maria-Pilar Barretina-Ginesta

Grupo Español de Investigación en Cáncer de Ovario (GEICO) and Medical Oncology Department, Institut Català d´Oncologia (ICO), Girona, Spain

D

David M. O’Malley

The Ohio State University and the James Comprehensive Cancer Center, Columbus, OH

B

Brigitte Honhon

Grand Hôpital de Charleroi, Charleroi, Belgium

C

Colleen C. McCormick

Legacy Medical Group Gynecologic Oncology, Portland, OR

S

Sakari Hietanen

Turku University Hospital and NSGO-CTU, Turku, Finland

R

Roisin E. O’Cearbhaill

Memorial Sloan Kettering Cancer Center and Weill Cornell Medical College, New York, NY

G

Giorgia Mangili

Department of Obstetrics and Gynecology, San Raffaele Hospital, Milan, Italy

R

Richard G. Moore

Division of Gynecologic Oncology, Wilmot Cancer Institute, Department of Obstetrics and Gynecology, University of Rochester, Rochester, NY

D

Dominique Berton

Institut de Cancerologie de l'Ouest, Saint-Herblain, France

R

Robert Allen Burger

Mersana Therapeutics, a Wholly Owned Subsidiary of Day One Biopharmaceuticals, Cambridge, MA

E

Elena Ioana Braicu

Department of Gynecology, Campus Virchow, Charité Universitätsmedizin Berlin and North Eastern German Society for Gynecologic Oncology (NOGGO), Berlin, Germany

B

Bradley J. Monk

M

Maria Jesús Rubio-Pérez

Hospital Universitario Reina Sofia and GEICO, Córdoba, Spain

N

Noelle Cloven

Texas Oncology, Fort Worth, Fort Worth, TX

C

Charlotte Aaquist Haslund

NSGO-CTU and Aalborg University Hospital, Aalborg, Denmark

T

Thomas J Herzog

University of Cincinnati Cancer Center; Department of Obstetrics & Gynecology, College of Medicine, Cincinnati, OH

L

Luda Shtessel

GSK, Durham, NC

J

Jonathan Lim

The University of Manchester & The Christie NHS Foundation Trust, Manchester, United Kingdom

A

Antonio Gonzalez Martin

Grupo Español de Investigación en Cáncer de Ovario (GEICO) and Medical Oncology Department, Clínica Universidad de Navarra, Madrid, Spain