Steroid Premedication and Monoclonal Antibody Therapy: Should We Reconsider?

被引:0
|
作者
Karlsen, Emma-Anne [1 ,2 ,3 ,4 ]
Walpole, Euan [3 ,5 ]
Simpson, Fiona [1 ,4 ]
机构
[1] Univ Queensland, Frazer Inst, Brisbane, Australia
[2] Mater Hosp Brisbane, Dept Gen Surg, Brisbane, Qld, Australia
[3] Univ Queensland, Sch Med, Brisbane, Qld, Australia
[4] Univ Queensland, Frazer Inst, Simpson Lab, 37 Kent St, Woolloongabba, Qld 4102, Australia
[5] Princess Alexandra Hosp, Div Canc Serv, Brisbane, Qld, Australia
基金
英国医学研究理事会;
关键词
Monoclonal antibodies; Antibody-dependent cell-mediated cytotoxicity (ADCC); Natural killer (NK) cells; Cetuximab; Trastuzumab; Monoclonal antibody premedication; Steroid; DEPENDENT CELLULAR CYTOTOXICITY; NATURAL-KILLER; TUMOR-CELLS; IN-VITRO; CETUXIMAB; GROWTH; INHIBITION; RECEPTORS; RITUXIMAB; HEAD;
D O I
10.1007/s11864-023-01170-4
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Monoclonal antibody (mAb) therapy is now considered a main component of cancer therapy in Australia. Although traditionally thought of as pure signalling inhibitors, a large proponent of these medications function through antibody-dependent cell-mediated cytotoxicity (ADCC). Currently, most protocols and institutional guidelines for ADCC-mediated mAbs promote the use of corticosteroids as premedication: this is implemented to reduce infusion-related reactions (IRRs) and antiemesis prophylaxis and combat concurrently administered chemotherapy-related syndromes. Concerningly, the inhibitory effects of ADCC by corticosteroids are well documented; henceforth, it is possible the current standard of care is misaligned to the literature surrounding ADCC. Subsequently, clinicians' decisions to act in contrast to this literature may be reducing the efficacy of mAbs. The literature suggests that the redundant use of corticosteroids should be cautioned against when used in conjunction with ADCC-mediated mAbs-this is due to the consequent reduction in anti-tumour activity. Owing to the fact IRRs typically occur upon initial infusion, the authors advocate for individual clinicians and institutional protocols to considering augmenting their practice to corticosteroid premedication at the first dose only, unless clinically indicated. Additionally, product information (PI) and consumer medicine information (CMI) documents distributed by Australian and international regulatory agencies should consider disclosing the risk of concurrent steroids with these medications. Moreover, the authors suggest considering alternative medications for the management of side effects.
引用
收藏
页码:275 / 283
页数:9
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