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Atezolizumab Combined With Platinum and Maintenance Niraparib for Recurrent Ovarian Cancer With a Platinum-Free Interval >6 Months: ENGOT-OV41/GEICO 69-O/ANITA Phase III Trial.
González-Martín, Antonio; Rubio, María Jesús; Heitz, Florian; Depont Christensen, René; Colombo, Nicoletta; Van Gorp, Toon; Romeo, Margarita; Ray-Coquard, Isabelle; Gaba, Lydia; Leary, Alexandra; De Sande, Luis Miguel; Lebreton, Coriolan; Redondo, Andrés; Fabbro, Michel; Barretina Ginesta, Maria-Pilar; Follana, Philippe; Pérez-Fidalgo, J Alejandro; Rodrigues, Manuel; Santaballa, Ana; Sabatier, Renaud; Bermejo-Pérez, Maria José; Lotz, Jean-Pierre; Pardo, Beatriz; Marquina, Gloria; Sánchez-Lorenzo, Luisa; Quindós, María; Estévez-García, Purificación; Guerra Alía, Eva; Manso, Luis; Casado, Victoria; Kommoss, Stefan; Tognon, Germana; Henry, Stéphanie; Bruchim, Ilan; Oaknin, Ana; Selle, Frédéric.
Afiliação
  • González-Martín A; Medical Oncology Department, Translational Oncology Group, CIMA, Universidad de Navarra, Cancer Center Clínica Universidad de Navarra, Madrid, Spain.
  • Rubio MJ; Grupo Español de Investigación en Cáncer ginecológicO (GEICO), Madrid, Spain.
  • Heitz F; Grupo Español de Investigación en Cáncer ginecológicO (GEICO), Madrid, Spain.
  • Depont Christensen R; Medical Oncology Department, Reina Sofia University Hospital of Cordoba, Cordoba, Spain.
  • Colombo N; Department for Gynaecology and Gynaecologic Oncology, Kliniken Essen-Mitte, Essen, Germany.
  • Van Gorp T; Department of Gynaecology, Berlin Institute of Health, Charité-Universitätsmedizin Berlin, Humboldt-Universität zu Berlin, Berlin, Germany.
  • Romeo M; Arbeitsgemeinschaft Gynaekologische Onkologie (AGO), Wiesbaden, Germany.
  • Ray-Coquard I; Grupo Español de Investigación en Cáncer ginecológicO (GEICO), Madrid, Spain.
  • Gaba L; Gynecologic Oncology Program, European Institute of Oncology, IRCCS, Milan, Italy.
  • Leary A; Department of Medicine and Surgery, University of Milan-Bicocca, Milan, Italy.
  • De Sande LM; Mario Negri Gynecologic Oncology Group (MaNGO), Milan, Italy.
  • Lebreton C; Division of Gynaecological Oncology, University Hospital Leuven, Leuven Cancer Institute, Leuven, Belgium.
  • Redondo A; Belgium and Luxembourg Gynaecological Oncology Group (BGOG), Leuven, Belgium.
  • Fabbro M; Medical Oncology Department, Institut Català d'Oncologia, Institut Germans Trias i Pujol (IGTP), Badalona, Spain.
  • Barretina Ginesta MP; Centre Leon Bérard and University of Lyon, Lyon, France.
  • Follana P; Centre Leon Bérard and University of Lyon, Lyon, France.
  • Pérez-Fidalgo JA; Groupe d'Investigateurs Nationaux pour l'Etude des Cancers Ovariens (GINECO), Paris, France.
  • Rodrigues M; Grupo Español de Investigación en Cáncer ginecológicO (GEICO), Madrid, Spain.
  • Santaballa A; Medical Oncology Department Hospital Clinic and Translational Genomics and Targeted Therapies in Solid Tumors, IDIBAPS, Barcelona, Spain.
  • Sabatier R; Groupe d'Investigateurs Nationaux pour l'Etude des Cancers Ovariens (GINECO), Paris, France.
  • Bermejo-Pérez MJ; Gustave Roussy, Villejuif, France.
  • Lotz JP; Grupo Español de Investigación en Cáncer ginecológicO (GEICO), Madrid, Spain.
  • Pardo B; Medical Oncology Service, Complejo Asistencial Universitario de León, León, Spain.
  • Marquina G; Groupe d'Investigateurs Nationaux pour l'Etude des Cancers Ovariens (GINECO), Paris, France.
  • Sánchez-Lorenzo L; Medical Oncology Department-Gynecologic Group, Institut Bergonié-Centre Régional de Lutte Contre le Cancer (CLCC), Bordeaux, France.
  • Quindós M; Grupo Español de Investigación en Cáncer ginecológicO (GEICO), Madrid, Spain.
  • Estévez-García P; Medical Oncology Department, Hospital Universitario La Paz-IdiPAZ, Madrid, Spain.
  • Guerra Alía E; Groupe d'Investigateurs Nationaux pour l'Etude des Cancers Ovariens (GINECO), Paris, France.
  • Manso L; Institut du Cancer de Montpellier Val d'Aurelle, Montpellier, France.
  • Casado V; Grupo Español de Investigación en Cáncer ginecológicO (GEICO), Madrid, Spain.
  • Kommoss S; Medical Oncology Department, Institut Català d'Oncologia, IDIBGI, Girona, Spain.
  • Tognon G; Groupe d'Investigateurs Nationaux pour l'Etude des Cancers Ovariens (GINECO), Paris, France.
  • Henry S; Centre Antoine Lacassagne, Nice, France.
  • Bruchim I; Grupo Español de Investigación en Cáncer ginecológicO (GEICO), Madrid, Spain.
  • Oaknin A; Medical Oncology Department, University Hospital of Valencia, INCLIVA Biomedical Research Institute, CIBERONC, Valencia, Spain.
  • Selle F; Groupe d'Investigateurs Nationaux pour l'Etude des Cancers Ovariens (GINECO), Paris, France.
J Clin Oncol ; : JCO2400668, 2024 Sep 18.
Article em En | MEDLINE | ID: mdl-39292975
ABSTRACT

PURPOSE:

To evaluate atezolizumab combined with platinum-based chemotherapy (CT) followed by maintenance niraparib for late-relapsing recurrent ovarian cancer.

METHODS:

The multicenter placebo-controlled double-blind randomized phase III ENGOT-OV41/GEICO 69-O/ANITA trial (ClinicalTrials.gov identifier NCT03598270) enrolled patients with measurable high-grade serous, endometrioid, or undifferentiated recurrent ovarian cancer who had received one or two previous CT lines (most recent including platinum) and had a treatment-free interval since last platinum (TFIp) of >6 months. Patients were stratified by investigator-selected carboplatin doublet, TFIp, BRCA status, and PD-L1 status in de novo biopsy and randomly assigned 11 to receive either atezolizumab or placebo throughout standard therapy comprising six cycles of a carboplatin doublet followed (in patients with response/stable disease) by maintenance niraparib until progression. The primary end point was investigator-assessed progression-free survival (PFS) per RECIST v1.1.

RESULTS:

Between November 2018 and January 2022, 417 patients were randomly assigned (15% BRCA-mutated, 36% PD-L1-positive, 66% TFIp >12 months, 11% previous poly [ADP-ribose] polymerase inhibitor after frontline CT, and 53% previous bevacizumab). Median follow-up was 28.6 months (95% CI, 26.6 to 30.5 months). Atezolizumab did not significantly improve PFS (hazard ratio, 0.89 [95% CI, 0.71 to 1.10]; P = .28). Median PFS was 11.2 months (95% CI, 10.1 to 12.1 months) with atezolizumab versus 10.1 months (95% CI, 9.2 to 11.2 months) with standard therapy. Subgroup analyses generally showed consistent results, including analyses by PD-L1 status. The objective response rate (ORR) was 45% (95% CI, 39 to 52) with atezolizumab and 43% (95% CI, 36 to 49) with standard therapy. The safety profile was as expected from previous experience of these drugs.

CONCLUSION:

Combining atezolizumab with CT and maintenance niraparib for late-relapsing recurrent ovarian cancer did not significantly improve PFS or the ORR.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article