Kapriniotis Konstantinos, Lampridis Savvas, Mitsos Sofoklis, Patrini Davide, Lawrence David R, Panagiotopoulos Nikolaos
Department of Thoracic Surgery, University College London Hospitals NHS Foundation Trust, London, United Kingdom.
Turk Thorac J. 2018 Oct;19(4):220-225. doi: 10.5152/TurkThoracJ.2018.18066. Epub 2018 Oct 1.
Multicentric Castleman disease (MCD) causes an extensive range of systematic symptoms and can be life-threatening if not treated promptly and appropriately. The pathophysiology of the disease remains unclear; however, interleukin 6 (IL-6) pathway and human herpesvirus 8 infection appear to play an important role. As a result, the treatment of MCD remains complex and often insufficient, although a plethora of therapeutic approaches have been used. Between these, biological agents in the form of monoclonal antibodies against specific pathogenic processes of the disease have improved survival rates significantly. In the present study, we review the clinical results of rituximab, which targets B lymphocytes, siltuximab and tocilizumab, which target the IL-6 pathway, bortezomib, which is a selective proteasome inhibitor, and anakinra, which is an interleukin 1 receptor antagonist. The introduction of these biological agents in the treatment of MCD appears to be promising in the first studies performed. However, more clinical trials are required to assess the efficacy and safety of each agent and to form therapeutic strategies that will be widely accepted.
多中心Castleman病(MCD)会引发一系列广泛的全身症状,若不及时、恰当地治疗,可能会危及生命。该病的病理生理学仍不明确;然而,白细胞介素6(IL-6)通路和人类疱疹病毒8感染似乎起着重要作用。因此,尽管已经采用了大量治疗方法,但MCD的治疗仍然复杂且往往效果不佳。其中,针对该疾病特定致病过程的单克隆抗体形式的生物制剂显著提高了生存率。在本研究中,我们回顾了利妥昔单抗(靶向B淋巴细胞)、西妥昔单抗和托珠单抗(靶向IL-6通路)、硼替佐米(一种选择性蛋白酶体抑制剂)以及阿那白滞素(一种白细胞介素1受体拮抗剂)的临床结果。在最初进行的研究中,这些生物制剂用于治疗MCD似乎前景良好。然而,需要更多的临床试验来评估每种药物的疗效和安全性,并形成被广泛接受的治疗策略。