Treatment of 120 adult osteosarcoma patients with metachronous and synchronous metastases: A retrospective series of the French Sarcoma Group — Elise Lavit (2021) | RDL Network
Treatment of 120 adult osteosarcoma patients with metachronous and synchronous metastases: A retrospective series of the French Sarcoma Group
Article 2021 en
Authors
EL
Elise Lavit
MA
Mihaela Aldea
SP
Sophie Piperno‐Neumann
Abstract
1 min read
Treatment options for metastatic osteosarcomas are scarce. Following failure of standard first line therapy, patients who relapse present a challenging treatment dilemma, and have a poor prognosis. Surgical removal of all metastases is essential. A retrospective analysis of patients with metastatic osteosarcomas was conducted in 15 French Sarcoma Group centers. From January 2009 to December 2018, we identified 120 adult patients; 36 with synchronous and 84 with metachronous metastases with 74 males and 46 females. Mean age was 30 years (18-53). Metastatic sites were lung, bone and other in 91, 11 and 24 patients, respectively. Mean time to first metachronous metastases was 22 months (4-97). All patients except 13 (10.8%) with metachronous metastases received a first line systemic treatment for relapse, and 39 patients (32.5%) were included in a clinical trial. Eighty-one patients (67.5%) had local treatment of distant metastases. Median progression free survival (PFS) and overall survival (OS) were 5.5 (95% CI 4.6-6.4) and 20.5 months (95% CI 13.2-27.7) respectively for the overall group. In multivariate analysis, more than five metastases, time to first metastases <24 months, were statistically significant negative prognostic factors for OS and PFS (P = .002, ≤.001 and P = .006, ≤.001, respectively). Surgery of metastases was associated with better prognosis on OS and PFS (P = .001 and .037, respectively). The presence of bone metastases was a negative prognostic factor on OS but not on PFS (P = .021). In reference sarcoma centers, relapsed osteosarcoma patients with more than one metastasis commonly receive more than one line of systemic therapy, and are included in clinical trial if available.
Maud Toulmonde, Derek Dinart, Mehdi Brahmi, Benjamin Verret, Myriam Jean‐Denis, Françoise Ducimetière, G. Désolneux, Pierre Méeus, Jean Palussière, Xavier Buy, Amine Bouhamama, P. Gillon, Armelle Dufresne, Clémence Hénon, François Le Loarer, Marie Karanian, Carine Ngo, Simone Mathoulin‐Pélissier, Carine Bellera, Axel Le Cesne, Jean Yves Blay, Antoîne Italiano
Dimitrios Bafaloukos, C. Papadimitriou, Helena Linardou, Gerasimos Aravantinos, Pavlos Papakostas, D. Skarlos, P. Kosmidis, George Fountzilas, Helen Gogas, Haralabos P. Kalofonos, Meletios A Dimopoulos
Pierre Kubicek, Axel Le Cesne, Cyril Lervat, Maud Toulmonde, Christine Chevreau, Florence Duffaud, Louis‐Romée Le Nail, Magali Morelle, Nathalie Gaspar, Cécile Verite, Marie‐Pierre Castex, Nicolas Penel, Esma Saâda, Sylvain Causeret, François Bertucci, Christophe Perrin, Emmanuelle Bompas, Daniel Orbach, Valérie Laurence, Sophie Piperno‐Neumann, Philippe Anract, María Rios, Jean‐Claude Gentet,
Nadia Hindi, Evan Rosenbaum, Emily Jonczak, Rainer Hamacher, Piotr Rutkowski, Anthony Frank Skryd, Elizabeth A. Connolly, Jean Yves Blay, Antonio Gutiérrez, Carolina Bogefors, Hans Gelderblom, Kjetil Boye, Clémence Hénon, Javier Martínez‐Trufero, José A. López-Martín, Andrés Redondo, Claudia Valverde, Bruno Vincenzi, William D. Tap, Javier Martín‐Broto
Discussion(0)
No comments yet. Be the first to comment.