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Niraparib Maintenance Therapy in Patients With Recurrent Ovarian Cancer After a Partial Response to the Last Platinum-Based Chemotherapy in the ENGOT-OV16/NOVA Trial.
Del Campo, Josep M; Matulonis, Ursula A; Malander, Susanne; Provencher, Diane; Mahner, Sven; Follana, Philippe; Waters, Justin; Berek, Jonathan S; Woie, Kathrine; Oza, Amit M; Canzler, Ulrich; Gil-Martin, Marta; Lesoin, Anne; Monk, Bradley J; Lund, Bente; Gilbert, Lucy; Wenham, Robert M; Benigno, Benedict; Arora, Sujata; Hazard, Sebastien J; Mirza, Mansoor R.
Afiliação
  • Del Campo JM; Grupo Español de Investigación en Cáncer de Ovario (GEICO) and Vall d'Hebrón University Hospital, Barcelona, Spain.
  • Matulonis UA; Dana-Farber Cancer Institute, Boston, MA.
  • Malander S; Nordic Society of Gynaecological Oncology (NSGO) and Lund University Hospital, Lund, Sweden.
  • Provencher D; Centre Hospitalier de L'Université de Montréal, Montreal, Quebec, Canada.
  • Mahner S; Arbeitsgemeinschaft Gynäkologische Onkologie (AGO) and University Hospital, Ludwig-Maximilians-University Munich, Munich, Germany.
  • Follana P; Groupe d'Investigateurs Nationaux pour l'Etude des Cancers Ovariens (GINECO) and Centre Antoine Lacassagne, Nice, France.
  • Waters J; National Cancer Research Institute (NCRI) and Kent Oncology Centre, Maidstone Hospital, Kent, United Kingdom.
  • Berek JS; Stanford Women's Cancer Center, Stanford Cancer Institute, Stanford, CA.
  • Woie K; Haukeland University Hospital, Bergen, Norway.
  • Oza AM; Princess Margaret Cancer Centre, University Health Network, Toronto, Ontario, Canada.
  • Canzler U; AGO and Technische Universität Dresden, Dresden, Germany.
  • Gil-Martin M; GEICO and Institut Català d'Oncologia-IDIBELL, L'Hospitalet, Barcelona, Spain.
  • Lesoin A; GINECO and Centre Oscar Lambret, Lille, France.
  • Monk BJ; Arizona Oncology (US Oncology Network), University of Arizona College of Medicine, Creighton University School of Medicine at St Joseph's Hospital, Phoenix, AZ.
  • Lund B; NSGO and Aalborg University Hospital, Aalborg, Denmark.
  • Gilbert L; McGill University, Research Institute, McGill University Health Centre, Montreal, Quebec, Canada.
  • Wenham RM; H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL.
  • Benigno B; Northside Hospital, Atlanta, GA.
  • Arora S; TESARO: A GSK Company, Waltham, MA.
  • Hazard SJ; TESARO: A GSK Company, Waltham, MA.
  • Mirza MR; NSGO and Rigshospitalet-Copenhagen University Hospital, Copenhagen, Denmark.
J Clin Oncol ; 37(32): 2968-2973, 2019 11 10.
Article em En | MEDLINE | ID: mdl-31173551
PURPOSE: In the ENGOT-OV16/NOVA trial (ClinicalTrials.gov identifier: NCT01847274), maintenance therapy with niraparib, a poly(ADP-ribose) polymerase inhibitor, prolonged progression-free survival in patients with platinum-sensitive, recurrent ovarian cancer who had a response to their last platinum-based chemotherapy. The objective of the study was to assess the clinical benefit and patient-reported outcomes in patients who had a partial response (PR) and complete response (CR) to their last platinum-based therapy. PATIENTS AND METHODS: A total of 553 patients were enrolled in the trial. Of 203 patients with a germline BRCA mutation (gBRCAmut), 99 had a PR and 104 had a CR to their last platinum-based therapy; of 350 patients without a confirmed gBRCAmut (non-gBRCAmut), 173 had a PR and 177 had a CR. Post hoc analyses were carried out to evaluate safety and the risk of progression in these patients according to gBRCAmut status and response to their last platinum-based therapy. Ovarian cancer-specific symptoms and quality of life were assessed using the Functional Assessment of Cancer Therapy-Ovarian Symptom Index. RESULTS: Progression-free survival was improved in patients treated with niraparib compared with placebo in both the gBRCAmut cohort (PR: hazard ratio [HR], 0.24; 95% CI, 0.131 to 0.441; P < .0001; CR: HR, 0.30; 95% CI, 0.160 to 0.546; P < .0001) and the non-gBRCAmut cohort (PR: HR, 0.35; 95% CI, 0.230 to 0.532; P < .0001; CR: HR, 0.58; 95% CI, 0.383 to 0.868; P = .0082). The incidence of any-grade and grade 3 or greater adverse events was manageable. No meaningful differences were observed between niraparib and placebo in PR and CR subgroups with respect to patient-reported outcomes. CONCLUSION: Patients achieved clinical benefit from maintenance treatment with niraparib regardless of response to the last platinum-based therapy.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Ovarianas / Piperidinas / Protocolos de Quimioterapia Combinada Antineoplásica / Inibidores de Poli(ADP-Ribose) Polimerases / Indazóis / Recidiva Local de Neoplasia Tipo de estudo: Clinical_trials Limite: Adult / Aged / Aged80 / Female / Humans / Middle aged Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Ovarianas / Piperidinas / Protocolos de Quimioterapia Combinada Antineoplásica / Inibidores de Poli(ADP-Ribose) Polimerases / Indazóis / Recidiva Local de Neoplasia Tipo de estudo: Clinical_trials Limite: Adult / Aged / Aged80 / Female / Humans / Middle aged Idioma: En Ano de publicação: 2019 Tipo de documento: Article