保乳治疗与乳房切除术

M. V. van Maaren, P. Poortmans, S. Siesling
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引用次数: 5

摘要

在临床实践中调查治疗效果时,关于使用随机对照试验(RCTs)还是观察性研究一直存在争议[1]。这尤其适用于保乳治疗(breast- conservation therapy, BCT)和乳房切除术(mastectomy, MAST)的比较,自我们的观察性研究在《柳叶刀肿瘤学》(Lancet Oncology)上发表以来,这一研究备受关注[2]。随机对照试验是高度赞赏的,因为它们接近于产生完全无偏的治疗比较估计。随机对照试验中的治疗组预期是可互换的;即使在比较组之间切换治疗,结果也将是相似的,并且仅仅是所研究治疗的效果。临床决定很大程度上是基于这类证据。但这总是最好的证据吗?它是否总是可行或合乎道德?在当前个性化医疗和“大数据”时代,对大量数据的临床解释(临床推理)变得越来越重要。它整合了所有可用的和相关的信息,可能有助于个体患者的最佳临床决策。这通常从现有的指南开始,通过从观察性研究和临床医生经验中提取的证据来完成[3]。重要的是,患者的偏好在(共同)决策中起着重要作用。一般来说,很难将随机对照试验的总体结果转化为单个患者对所研究治疗的反应。即使对于与试验人群具有相同特征的患者,rct中观察到的总体治疗效果也只有在每个个体参与者中治疗获益和损害的概率均匀分布的情况下才适用[3]。通常,形成治疗指南基础的证据是基于很久以前进行的随机对照试验,而观察性研究包括最近诊断的人群。对于BCT和MAST,试验都是在80年代进行的。RCT人群与现实世界人群之间的另一个重要差异是后者中老年乳腺癌患者的比例不断增加。这不仅是由于人口老龄化,也是由于国家筛查方案对乳腺癌的早期发现(荷兰的年龄上限为75岁),导致老年人发病率较高。此外,诊断和外科手术以及局部和全身治疗也有了很大的改善。此外,对乳腺肿瘤生物学特征的了解不断增加,导致了更先进的肿瘤定向治疗的引入。这些改进的结合很可能会……
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Breast-conserving therapy versus mastectomy
There is an ongoing debate regarding the use of randomised controlled trials (RCTs) versus observational studies when investigating treatment effects in clinical practice [1]. This holds especially true for the comparison of breast-conserving therapy (BCT) and mastectomy (MAST), which gained much attention since the publication of our observational study in Lancet Oncology [2]. RCTs are highly appreciated as they are close to generate perfectly unbiased treatment comparison estimates. Treatment groups in a RCT are expected to be exchangeable; even when switching the treatment between the compared groups, results will be similar and are solely the effect of the treatment under study. Clinical decisions are largely based on this type of evidence. But is this always the best evidence? Is it always feasible or ethical? In the current era of personalised medicine and 'big data', clinical interpretation of an abundance of data (clinical reasoning) is becoming more and more crucial. It integrates all available and relevant information that may contribute to the best clinical decision-making for individual patients. This generally starts with existing guidelines, completed by evidence extracted from observational studies and clinicians' experiences [3]. Importantly, the patient's preference plays an important role in (shared) decision-making. In general, it is difficult to translate the overall results of a RCT in the response of an individual patient to the investigated treatment. Even for patients with identical characteristics to those in the trial population, the overall treatment effect observed in RCTs would only apply if the probability of treatment benefit and detriment was equally distributed in every individual participant [3]. Often, evidence forming the basis of treatment guidelines are based on RCTs conducted a long time ago, while observational studies include a more recently diagnosed population. For BCT and MAST, the trials were all conducted in the eighties. Another important discrepancy between the RCT populations and the real-world population is the increasing share of elderly breast cancer patients in the latter. This is not only due to the ageing population, but also to early detection of breast cancer in the national screening program (which upper age limit is 75 years in the Netherlands), leading to a higher incidence in the elderly. Furthermore, diagnostic and surgical procedures as well as local and systemic therapies improved considerably. Moreover, increasing knowledge about the biological features of breast tumours led to the introduction of more advanced tumour-directed therapies. The combination of these improvements are very likely to …
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