| Literature DB >> 31318983 |
Eric Voog1, Boris Campillo-Gimenez2, Claude Elkouri3, Franck Priou4, Frederic Rolland5, Brigitte Laguerre2, Chaza Elhannani6, Jacques Merrer7, Christian Pfister8, Emmanuel Sevin9, Tifenn L'Haridon4, Ali Hasbini7, Laura Moise9, Annick Le Rol10, Jean Pierre Malhaire11, Remy Delva5, Elodie Vauléon2, Oana Cojocarasu12, Philippe Deguiral13, Isabelle Cumin14, Caroline Cheneau11,14, Friedrike Schlürmann10,11, Valérie Delecroix13, Elouen Boughalem5, Delphine Mollon10, Catherine Ligeza-Poisson13, Sophie Abadie-Lacourtoisie5, Erik Monpetit15, Thierry Chatellier13, Henry Desclos16, Elodie Coquan9, Florence Joly9, Jean Yves Tessereau5,17, Sandra Dupuy5, Delphine Déniel Lagadec11,17, Fanny Marhuenda5,17, Francoise Grudé5,17.
Abstract
The treatment landscape in metastatic renal cell carcinoma has changed fundamentally over the last decade by the development of antiangiogenic agents, mammalian target of rapamycin inhibitors and immunotherapy. Outside of the context of a clinical trial, the treatments are used sequentially. We describe results under real-life conditions of a sequential treatment strategy, before the era of immunotherapy. All patients were treated according to their prognostic score (either Memorial Sloan Kettering Cancer Center or International Metastatic Renal Cell Carcinoma Database Consortium) for advanced renal cell carcinoma. A treatment strategy involving 1 to 4 lines was determined including a rechallenge criterion for the repeat use of a treatment class. Three hundred forty-four patients were included over 3 years. Overall survival was 57 months in patients with good or intermediate prognosis and 19 months in patients with poor prognosis. In the former group, the proportions of patients treated with 2 to 4 treatment lines were 70%, 38% and 16%, respectively. The best objective response rates for lines 1 to 4 were 46%, 36%, 16% and 17%, respectively. Grade III/IV toxicity did not appear to be cumulative. The recommended strategy was followed in 68% of patients. A large proportion of patients with good or intermediate prognosis who progress after two lines of treatment still have a performance status good enough to receive a systemic treatment, which justifies such a strategy. Overall survival of patients with good and intermediate prognosis was long, suggesting a benefit from the applied approach. These results might be used as selection criterion for the treatment of patients in the era of immune checkpoint inhibitors.Entities:
Keywords: anti-angiogenesis agents; overall survival; real life conditions; renal cell carcinoma; sequential treatments
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Year: 2019 PMID: 31318983 DOI: 10.1002/ijc.32578
Source DB: PubMed Journal: Int J Cancer ISSN: 0020-7136 Impact factor: 7.396