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早期肿瘤学临床试验中的性别作为生物学变量:推动个性化医疗之路

Sex as a Biological Variable in Early-Phase Oncology Clinical Trials: Enhancing the Path to Personalised Medicine.

作者信息

Sutherland Lydia, Carter Louise

机构信息

Division of Cancer Sciences, School of Medical Sciences, University of Manchester, Manchester, UK.

Department of Pharmacy, The Christie NHS Foundation Trust, Manchester, UK.

出版信息

Heliyon. 2024 Jun 7;10(12):e32597. doi: 10.1016/j.heliyon.2024.e32597. eCollection 2024 Jun 30.

Abstract

Sex is an essential biological variable that influences the development, progression and response to treatment in cancer. Despite this, early-phase cancer clinical trials frequently neglect to consider sex as a variable, creating a barrier to the development of personalised medicine. This article argues that failure to identify and infer sex differences in early-phase clinical trials may result in suboptimal dosing, underestimation of toxicity, and the failure to identify potential sex-specific responses to new systemic anticancer therapies. There should be a greater focus on sex as a biological variable in drug development so that thoughtful and deliberate study design can bring precision to the development of new systemic cancer therapies.

摘要

性别是一个重要的生物学变量,它会影响癌症的发展、进程及对治疗的反应。尽管如此,早期癌症临床试验常常忽视将性别作为一个变量来考虑,这为个性化医疗的发展造成了障碍。本文认为,在早期临床试验中未能识别和推断性别差异可能会导致给药剂量欠佳、对毒性的低估,以及无法识别新的全身性抗癌疗法潜在的性别特异性反应。在药物研发中,应更多地关注性别这一生物学变量,以便经过深思熟虑的研究设计能够为新的全身性癌症疗法的研发带来精准性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fa3/11341330/9c80657e09aa/gr1.jpg

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