Bernardo Rossini, Nicola Cecchi, Felice Clemente, Maria Rosaria De Paolis, Stefan Hohaus, Vanessa Innao, Mariano Lucignano, Roberto Massaiu, Giovanna Palumbo, Gian Matteo Rigolin, Francesca Gaia Rossi, Luisa Verga, Attilio Guarini
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引用次数: 0
摘要
卡斯特曼病(CD)是一组淋巴细胞增生性疾病,具有共同的组织病理学特征,但病因、临床特征、严重程度、治疗方法和疗效却大相径庭。目前,西妥昔单抗是美国食品药品管理局(FDA)和欧洲药品管理局(EMA)批准用于特发性多中心 CD 的唯一疗法,并被治疗指南推荐为一线疗法。尽管西妥昔单抗的治疗在临床试验中得到了广泛的表征,但现实世界中的可用证据仍然很少。本临床经验集重点关注接受西妥昔单抗治疗的患者,尤其是特发性多中心 CD 诊断工作,以及进入 CD 或伴随疾病鉴别诊断的复杂疾病患者的治疗管理。因此,从长期用药的有效性和安全性以及治疗中断的后果来看,这些数据有助于进一步描述和改进在实际应用中使用西妥昔单抗的情况。
Real-practice management and treatment of idiopathic multicentric Castleman disease with siltuximab: a collection of clinical experiences.
Castleman disease (CD) is a group of lymphoproliferative disorders that share common histopathological features yet have widely different aetiologies, clinical features and grades of severity as well as treatments and outcomes. Siltuximab is currently the only therapy approved by the FDA and EMA for idiopathic multicentric CD and is recommended as first-line therapy in treatment guidelines. Despite the extensive characterization of siltuximab treatment in clinical trials, available evidence from real-world practice is still scant. This collection of clinical experiences focuses on patients treated with siltuximab therapy, particularly regarding the idiopathic multicentric CD diagnostic work-up, and on treatment administration in patients with complex disease entering differential diagnosis with CD or concomitant diseases. Thus, these data help further characterize and improve the use of siltuximab in real practice in terms of effectiveness and safety of long-term administration as well as consequences of treatment interruption.
期刊介绍:
Covers all phases of original research: laboratory, animal and human/clinical studies, health economics and outcomes research, and postmarketing studies. Original research that shows positive or negative results are welcomed. Invited review articles may cover single-drug reviews, drug class reviews, latest advances in drug therapy, therapeutic-area reviews, place-in-therapy reviews, new pathways and classes of drugs. In addition, systematic reviews and meta-analyses are welcomed and may be published as original research if performed per accepted guidelines. Editorials of key topics and issues in drugs and therapeutics are welcomed. The Editor-in-Chief will also consider manuscripts of interest in areas such as technologies that support diagnosis, assessment and treatment. EQUATOR Network reporting guidelines should be followed for each article type. GPP3 Guidelines should be followed for any industry-sponsored manuscripts. Other Editorial sections may include Editorial, Case Report, Conference Report, Letter-to-the-Editor, Educational Section.