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Health-related quality of life in patients with a germline BRCA mutation and metastatic pancreatic cancer receiving maintenance olaparib.
Hammel, P; Kindler, H L; Reni, M; Van Cutsem, E; Macarulla, T; Hall, M J; Park, J O; Hochhauser, D; Arnold, D; Oh, D-Y; Reinacher-Schick, A; Tortora, G; Algül, H; O'Reilly, E M; McGuinness, D; Cui, K Y; Joo, S; Yoo, H K; Patel, N; Golan, T.
Affiliation
  • Hammel P; Department of Digestive Oncology, Hôpital Beaujon (AP-HP), Clichy, and University Paris VII, Paris, France. Electronic address: pascal.hammel@aphp.fr.
  • Kindler HL; Department of Medicine, Section of Hematology/Oncology, University of Chicago, Chicago, USA.
  • Reni M; Department of Oncology, IRCCS Ospedale San Raffaele Scientific Institute, Milan, Italy.
  • Van Cutsem E; Division of Digestive Oncology, University Hospitals Gasthuisberg and KU Leuven, Leuven, Belgium.
  • Macarulla T; Department of Medical Oncology, Vall d'Hebron University Hospital and Vall d'Hebron Institute of Oncology, Barcelona, Spain.
  • Hall MJ; Department of Medical Oncology, Fox Chase Cancer Center, Philadelphia, USA.
  • Park JO; Division of Hematology-Oncology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea.
  • Hochhauser D; Department of Oncology, University College London Cancer Institute, London, UK.
  • Arnold D; Department of Oncology, Asklepios Tumorzentrum Hamburg Asklepios Klinik Altona, Hamburg, Germany.
  • Oh DY; Department of Internal Medicine, Seoul National University Hospital, Cancer Research Institute, Seoul National University College of Medicine, Seoul, South Korea.
  • Reinacher-Schick A; Department of Hematology, Oncology and Palliative Care, St. Josef-Hospital, Ruhr University Bochum, Bochum, Germany.
  • Tortora G; Department of Medicine, Section of Medical Oncology, Azienda Ospedaliera Universitaria Integrata Verona, Verona and Fondazione Policlinico Universitario Gemelli IRCCS, Rome, Italy.
  • Algül H; Second Department of Internal Medicine, Klinikum rechts der Isar, Comprehensive Cancer Center Munich-TUM and Department of Internal Medicine II, Technische Universität München, Munich, Germany.
  • O'Reilly EM; Gastrointestinal Oncology Service, Memorial Sloan Kettering Cancer Center, New York, USA.
  • McGuinness D; AstraZeneca, Cambridge, UK.
  • Cui KY; AstraZeneca, Gaithersburg, USA.
  • Joo S; Merck & Co., Inc., Kenilworth, USA.
  • Yoo HK; AstraZeneca, Cambridge, UK.
  • Patel N; AstraZeneca, Gaithersburg, USA.
  • Golan T; The Oncology Institute, Sheba Medical Center, Tel Aviv, Israel.
Ann Oncol ; 30(12): 1959-1968, 2019 12 01.
Article in En | MEDLINE | ID: mdl-31562758
ABSTRACT

BACKGROUND:

Patients with metastatic pancreatic cancer often have a detriment in health-related quality of life (HRQoL). In the randomized, double-blind, phase III POLO trial progression-free survival was significantly longer with maintenance olaparib, a poly(ADP-ribose) polymerase inhibitor, than placebo in patients with a germline BRCA1 and/or BRCA2 mutation (gBRCAm) and metastatic pancreatic cancer whose disease had not progressed during first-line platinum-based chemotherapy. The prespecified HRQoL evaluation is reported here. PATIENTS AND

METHODS:

Patients were randomized to receive maintenance olaparib (300 mg b.i.d.; tablets) or placebo. HRQoL was assessed using the European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire Core 30-item module at baseline, every 4 weeks until disease progression, at discontinuation, and 30 days after last dose. Scores ranged from 0 to 100; a ≥10-point change or difference between arms was considered clinically meaningful. Adjusted mean change from baseline was analysed using a mixed model for repeated measures. Time to sustained clinically meaningful deterioration (TSCMD) was analysed using a log-rank test.

RESULTS:

Of 154 randomized patients, 89 of 92 olaparib-arm and 58 of 62 placebo-arm patients were included in HRQoL analyses. The adjusted mean change in Global Health Status (GHS) score from baseline was <10 points in both arms and there was no significant between-group difference [-2.47; 95% confidence interval (CI) -7.27, 2.33; P = 0.31]. Analysis of physical functioning scores showed a significant between-group difference (-4.45 points; 95% CI -8.75, -0.16; P = 0.04). There was no difference in TSCMD for olaparib versus placebo for GHS [P = 0.25; hazard ratio (HR) 0.72; 95% CI 0.41, 1.27] or physical functioning (P = 0.32; HR 1.38; 95% CI 0.73, 2.63).

CONCLUSIONS:

HRQoL was preserved with maintenance olaparib treatment with no clinically meaningful difference compared with placebo. These results support the observed efficacy benefit of maintenance olaparib in patients with a gBRCAm and metastatic pancreatic cancer. CLINCALTRIALS.GOV NUMBER NCT02184195.
Subject(s)
Key words

Full text: 1 Database: MEDLINE Main subject: Pancreatic Neoplasms / Phthalazines / Piperazines / BRCA1 Protein / BRCA2 Protein / Poly(ADP-ribose) Polymerase Inhibitors Type of study: Clinical_trials / Prognostic_studies Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Year: 2019 Type: Article

Full text: 1 Database: MEDLINE Main subject: Pancreatic Neoplasms / Phthalazines / Piperazines / BRCA1 Protein / BRCA2 Protein / Poly(ADP-ribose) Polymerase Inhibitors Type of study: Clinical_trials / Prognostic_studies Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Year: 2019 Type: Article