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).
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
Journal Info
Journal of Clinical Oncology
Lippincott Williams & Wilkins
Authors (20)
Mark S. Shahin
PennState Health, Hershey
Maria-Pilar Barretina-Ginesta
Grupo Español de Investigación en Cáncer de Ovario (GEICO) and Medical Oncology Department, Institut Català d´Oncologia (ICO), Girona, Spain
David M. O’Malley
The Ohio State University and the James Comprehensive Cancer Center, Columbus, OH
Brigitte Honhon
Grand Hôpital de Charleroi, Charleroi, Belgium
Colleen C. McCormick
Legacy Medical Group Gynecologic Oncology, Portland, OR
Sakari Hietanen
Turku University Hospital and NSGO-CTU, Turku, Finland
Roisin E. O’Cearbhaill
Memorial Sloan Kettering Cancer Center and Weill Cornell Medical College, New York, NY
Giorgia Mangili
Department of Obstetrics and Gynecology, San Raffaele Hospital, Milan, Italy
Richard G. Moore
Division of Gynecologic Oncology, Wilmot Cancer Institute, Department of Obstetrics and Gynecology, University of Rochester, Rochester, NY
Dominique Berton
Institut de Cancerologie de l'Ouest, Saint-Herblain, France
Robert Allen Burger
Mersana Therapeutics, a Wholly Owned Subsidiary of Day One Biopharmaceuticals, Cambridge, MA
Elena Ioana Braicu
Department of Gynecology, Campus Virchow, Charité Universitätsmedizin Berlin and North Eastern German Society for Gynecologic Oncology (NOGGO), Berlin, Germany
Bradley J. Monk
Maria Jesús Rubio-Pérez
Hospital Universitario Reina Sofia and GEICO, Córdoba, Spain
Noelle Cloven
Texas Oncology, Fort Worth, Fort Worth, TX
Charlotte Aaquist Haslund
NSGO-CTU and Aalborg University Hospital, Aalborg, Denmark
Thomas J Herzog
University of Cincinnati Cancer Center; Department of Obstetrics & Gynecology, College of Medicine, Cincinnati, OH
Luda Shtessel
GSK, Durham, NC
Jonathan Lim
The University of Manchester & The Christie NHS Foundation Trust, Manchester, United Kingdom
Antonio Gonzalez Martin
Grupo Español de Investigación en Cáncer de Ovario (GEICO) and Medical Oncology Department, Clínica Universidad de Navarra, Madrid, Spain