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Real-world clinical and survival outcomes of patients with early relapsed triple-negative breast cancer from the ESME national cohort

医学 内科学 危险系数 紫杉烷 肿瘤科 队列 乳腺癌 蒽环类 转移性乳腺癌 化疗 癌症 三阴性乳腺癌 比例危险模型 置信区间
作者
Thomas Grinda,Alison Antoine,William Jacot,Paul Cottu,Thibault De La Motte Rouge,Jean‐Sébastien Frénel,Audrey Mailliez,Florence Dalenc,Anthony Gonçalvès,Florian Clatot,Marie‐Ange Mouret‐Reynier,Christelle Lévy,Jean-­Marc Ferrero,Isabelle Desmoulins,Lionel Uwer,Thierry Petit,Christelle Jouannaud,Mónica Arnedos,Michaël Chevrot,Coralie Courtinard
出处
期刊:European Journal of Cancer [Elsevier]
卷期号:189: 112935-112935 被引量:16
标识
DOI:10.1016/j.ejca.2023.05.023
摘要

Early metastatic relapse of triple-negative breast cancer (mTNBC) after anthracyclins and/or taxanes based (A/T) primary treatment represents a highly aggressive cancer situation requiring urgent characterisation and handling. Epidemio-Strategy-Medico-Economical-Metastatic Breast Cancer (ESME-MBC) database, a multicenter, national, observational cohort (NCT03275311) provides recent data on this entity.All ESME patients diagnosed between 2008 and 2020 with mTNBC occurring as a relapse after a systemic neoadjuvant/adjuvant taxane and/or anthracycline-based chemotherapy were included. Early relapses were defined by a metastatic diagnosis up to 12 months of the end of neo/adjuvant A/T chemotherapy. We assessed overall survival (OS) and progression-free-survival under first-line treatment (PFS1) by early versus late relapse (≥12 months).Patients with early relapse (N = 881, 46%) were younger and had a larger tumour burden at primary diagnosis than those with late relapses (N = 1045). Early relapse rates appeared stable over time. Median OS was 10.1 months (95% CI 9.3-10.9) in patients with early relapse versus 17.1 months (95% CI 15.7-18.2) in those with late relapse (adjusted hazard-ratio (aHR): 1.92 (95% CI 1.73-2.13); p < 0.001). The median PFS1 was respectively 3.1 months (95% CI 2.9-3.4) and 5.3 months (95% CI 5.1-5.8); (aHR: 1.66; [95% CI 1.50-1.83]; p < 0.001). Among early relapsed patients, a higher number of metastatic sites, visceral disease but not treatment types, were independently associated with a poorer OS.These real-world data provide strong evidence on the dismal prognosis, higher treatment resistance and major unmet medical need associated with early relapsed mTNBC. Database registration: clinicaltrials.gov Identifier NCT032753.
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