Your browser doesn't support javascript.
loading
Efficacy and safety of regorafenib in patients with metastatic or locally advanced chondrosarcoma: Results of a non-comparative, randomised, double-blind, placebo controlled, multicentre phase II study.
Duffaud, Florence; Italiano, Antoine; Bompas, Emannuelle; Rios, Maria; Penel, Nicolas; Mir, Olivier; Piperno-Neumann, Sophie; Chevreau, Christine; Delcambre, Corinne; Bertucci, François; Boudou-Rouquette, Pascaline; Cancel, Mathilde; Perrin, Christophe; Saada-Bouzid, Esma; Monard, Laure; Schiffler, Camille; Chaigneau, Loic; Hervieu, Alice; Collard, Olivier; Bouvier, Corinne; Vidal, Vincent; Chabaud, Sylvie; Blay, Jean-Yves.
Afiliación
  • Duffaud F; Aix Marseille Univ, APHM Hopital La Timone, Medical Oncology Unit, Marseille, France. Electronic address: florence.duffaud@ap-hm.fr.
  • Italiano A; Medical Oncology Unit, Institut Bergonié, Bordeaux, France.
  • Bompas E; Medical Oncology Department, Centre René Gauducheau, Saint Herblain, France.
  • Rios M; Medical Oncology, Institut de Cancérologie de Lorraine - Alexis Vautrin, Vandoeuvre Les Nancy, France.
  • Penel N; Medical Oncology Department, Centre Oscar Lambret and Lille University Hospital, Lille, France.
  • Mir O; Medical Oncology Department, Gustave Roussy, Villejuif, France.
  • Piperno-Neumann S; Medical Oncology Department, Institut Curie, Paris, France.
  • Chevreau C; Medical Oncology Department, Institut Universitaire de Cancérologie de Toulouse, Oncopole, Toulouse, France.
  • Delcambre C; Medical Oncology Department, Centre François Baclesse, Caen, France.
  • Bertucci F; Medical Oncology Department, Institut Paoli-Calmettes, Marseille, France.
  • Boudou-Rouquette P; Medical Oncology Department, Centre Hospitalier Universitaire Cochin, APHP, Paris, France.
  • Cancel M; Medical Oncology Department, Centre Hospitalier Régional Universitaire Bretonneau, Tours, France.
  • Perrin C; Medical Oncology Unit, Centre Eugène Marquis, Rennes, France.
  • Saada-Bouzid E; Medical Oncology Department, Centre Antoine Lacassagne, Nice, France.
  • Monard L; Unicancer, Paris, France.
  • Schiffler C; Department of Statistics, Centre Léon Bérard, Lyon, France.
  • Chaigneau L; Medical Oncology Department, Centre Hospitalier Universitaire - Jean Minjoz Hospital, Besançon, France.
  • Hervieu A; Medical Oncology Department, Centre Georges Francois Leclerc, Dijon, France.
  • Collard O; Medical Oncology Department, Institut de Cancérologie Lucien Neuwirth, St Priest En Jarez, France.
  • Bouvier C; Aix Marseille Univ, APHM Hopital La Timone, Pathology Department, Marseille, France.
  • Vidal V; Aix Marseille Univ, APHM Hopital La Timone, Radiology Department, Marseille, France.
  • Chabaud S; Department of Statistics, Centre Léon Bérard, Lyon, France.
  • Blay JY; Medical Oncology Department, Centre Léon Bérard, Lyon, France.
Eur J Cancer ; 150: 108-118, 2021 06.
Article en En | MEDLINE | ID: mdl-33895682
BACKGROUND: This multi-cohort trial explored the efficacy and safety of regorafenib for patients with advanced sarcomas of bone origin; this report details the cohort of patients with metastatic or locally advanced chondrosarcoma (CS), progressing after prior chemotherapy. PATIENTS AND METHODS: Patients with CS, progressing despite prior standard therapy, were randomised (2:1) to receive regorafenib or placebo. Patients on placebo could crossover to receive regorafenib after centrally confirmed progressive disease. The primary endpoint was progression-free rate (PFR) at 12 weeks. With one-sided α of 0.05, and 80% power, at least 16/24 progression-free patients at 12 weeks were needed for success (P0 = 50%, P1 = 75%). RESULTS: From September 2014 to February 2019, 46 patients were included in the CS cohort, and 40 patients were evaluable for efficacy: 16 on placebo and 24 on regorafenib. Thirteen patients (54.2%; 95% CI [35.8%-[) were non-progressive at 12 weeks on regorafenib versus 5 (31.3%; 95% CI [13.2%-[);) on placebo. Median PFS was 19.9 weeks on regorafenib, and 8.0 on placebo. Fourteen placebo patients crossed over to regorafenib after progression. The most common grade ≥3 treatment-related adverse events on regorafenib included hypertension (12%), asthenia (8%), thrombocytopenia (8%) and diarrhoea (8%). One episode of fatal liver dysfunction occurred on regorafenib. CONCLUSION: Although the primary endpoint was not met statistically in this small randomised cohort, there is modest evidence to suggest that regorafenib might slow disease progression in patients with metastatic CS after the failure of prior chemotherapy. CLINICAL TRIAL REGISTRATION: The trial is registered at ClinicalTrials.gov (NCT02389244).
Asunto(s)
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Compuestos de Fenilurea / Piridinas / Neoplasias Óseas / Condrosarcoma / Antineoplásicos Tipo de estudio: Clinical_trials Límite: Adult / Aged / Female / Humans / Male / Middle aged País/Región como asunto: Europa Idioma: En Revista: Eur J Cancer Año: 2021 Tipo del documento: Article Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Compuestos de Fenilurea / Piridinas / Neoplasias Óseas / Condrosarcoma / Antineoplásicos Tipo de estudio: Clinical_trials Límite: Adult / Aged / Female / Humans / Male / Middle aged País/Región como asunto: Europa Idioma: En Revista: Eur J Cancer Año: 2021 Tipo del documento: Article Pais de publicación: Reino Unido