Change of dosing paradigm in oncology

Q4 Medicine Forum of Clinical Oncology Pub Date : 2024-05-20 DOI:10.2478/fco-2023-0022
Sophia Papakatsika, Myrsini Orfanidou, Elpiniki Rentzeperi, Christos Emmanouilides
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Abstract

Drug dosing based on the body surface area (BSA) has been the mainstay of oncological treatment over the last decades. Although this seems to be an adequate measure of an individual’s appropriate dose for traditional chemotherapeutic drugs according to their somatometric data, it is currently being questioned due to the delivery of novel treatments such as monoclonal antibodies. Most modern regimes require either a flat (fixed)-dosing model, independent of body weight, or a weight-based administration pattern, mainly depending on specific pharmacokinetic data. However, even in this case, some controversy exists about whether this model is sufficient. Given the recent findings from pharmacokinetic studies, perhaps we should reconsider the solid hypothesis that drug efficacy correlates with dose, as many molecules seem to be efficient even in the lowest doses administered, with minimum toxicity.
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改变肿瘤学的用药模式
过去几十年来,基于体表面积(BSA)的药物剂量一直是肿瘤治疗的主流。虽然根据体表面积数据来确定传统化疗药物的适当剂量似乎已经足够,但由于单克隆抗体等新型疗法的出现,这种方法目前正受到质疑。大多数现代治疗方案都要求采用与体重无关的统一(固定)给药模式,或基于体重的给药模式,主要取决于特定的药代动力学数据。然而,即使在这种情况下,这种模式是否足够也存在一些争议。鉴于药代动力学研究的最新发现,也许我们应该重新考虑药物疗效与剂量相关这一坚实的假设,因为许多分子似乎即使在给药剂量最低的情况下也是有效的,而且毒性最小。
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来源期刊
Forum of Clinical Oncology
Forum of Clinical Oncology Medicine-Oncology
CiteScore
0.50
自引率
0.00%
发文量
3
审稿时长
6 weeks
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