Long-term Outcomes of Oral Vinorelbine in Advanced, Progressive Desmoid Fibromatosis and Influence of CTNNB1 Mutational Status

التفاصيل البيبلوغرافية
العنوان: Long-term Outcomes of Oral Vinorelbine in Advanced, Progressive Desmoid Fibromatosis and Influence of CTNNB1 Mutational Status
المؤلفون: Françoise Rimareix, Olivier Mir, Leila Haddag-Miliani, Etienne Rouleau, Charles Honoré, Olaf Mercier, Carine Ngo, Anaïs Brunet, Andrea Cavalcanti, Charles Court, Sarah Dumont, Sylvain Briand, Axel Le Cesne, Cécile Le Péchoux, Julien Domont, Antonin Levy, Elie Fadel, Julien Adam, Ali N. Chamseddine, Matthieu Faron, Arnaud Bayle
المصدر: Clinical Cancer Research. 26:6277-6283
بيانات النشر: American Association for Cancer Research (AACR), 2020.
سنة النشر: 2020
مصطلحات موضوعية: 0301 basic medicine, Cancer Research, medicine.medical_specialty, business.industry, Fibromatosis, Cancer, Neutropenia, Vinorelbine, medicine.disease, Gastroenterology, Confidence interval, 03 medical and health sciences, Regimen, 030104 developmental biology, 0302 clinical medicine, Oncology, 030220 oncology & carcinogenesis, Concomitant, Internal medicine, Medicine, business, Progressive disease, medicine.drug
الوصف: Purpose: Desmoid-type fibromatosis (DF) are locally aggressive neoplasms, with a need for effective systemic treatment in case of progression to avoid the short- and long-term complications of local treatments. Experimental Design: We retrospectively analyzed the outcomes of adult patients with DF treated with oral vinorelbine (90 mg once weekly) at Gustave Roussy Cancer Institute (Villejuif, Paris, France). Only patients with documented progressive disease according to RECIST v1.1 for more than 3 months (±2 weeks) before treatment initiation were included. Results: From 2009 to 2019, 90 out of 438 patients with DF were eligible for this analysis. Vinorelbine was given alone in 56 patients (62%), or concomitantly with endocrine therapy in 34 patients, for a median duration of 6.7 months. A partial response was observed in 29% and stable disease in another 57%. With a median follow-up of 52.4 months, the median time to treatment failure (TTF) was not reached. Progression-free rates at 6 and 12 months were 88.7% and 77.5%, respectively. Concomitant endocrine therapy was associated with longer TTF in women [HR, 2.16; 95% confidence interval (CI), 1.06–4.37; P = 0.03). Among 64 patients with documented CTNNB1 mutational status, p.S45F or p.S45P mutations were associated with longer TTF compared with p.T41A or wild-type tumors (HR, 2.78; 95% CI, 1.23–6.27; P = 0.04). Toxicity profile was favorable, without grade 3–4 toxicity, except for one grade 3 neutropenia. Conclusions: Oral vinorelbine is an effective, affordable, and well-tolerated regimen in patients with advanced, progressive DF. Prolonged activity was observed in patients with tumors harboring CTNNB1 p.S45F or p.S45P mutations.
تدمد: 1557-3265
1078-0432
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::c9c75798305cffc234b5488f4e17b9c3Test
https://doi.org/10.1158/1078-0432.ccr-20-1847Test
حقوق: OPEN
رقم الانضمام: edsair.doi...........c9c75798305cffc234b5488f4e17b9c3
قاعدة البيانات: OpenAIRE