Rubovszky Gabor
Department of Thoracic and Abdominal Tumors and Clinical Pharmacology and the National Tumor Biology Laboratory, National Institute of Oncology, Budapest, Hungary.
Department of Oncology, Semmelweis University, Budapest, Hungary.
Ann Transl Med. 2024 Aug 1;12(4):68. doi: 10.21037/atm-23-1583. Epub 2023 Dec 4.
In hormone-receptor-positive (HR) and human epidermal growth factor receptor 2-negative (HER2) metastatic breast cancer endocrine-based therapies are preferred over chemotherapy. One of the treatment options is the combination of everolimus with exemestane or other endocrine drug in later lines mainly based on progression-free survival (PFS) results of the phase 3 BOLERO-2 trial. Altogether, clinical trials did not prove an overall survival (OS) benefit and considerable side effects hampered its application in the day-by-day practice. In recent years CDK4/6-inhibitors became a first-choice combination partner to the endocrine treatment, everolimus still has a place within the treatment armamentarium. Although everolimus is a targeted drug, there is no accepted predictive biomarker and further patient selection is not possible. However, several directions can be defined how to optimally use everolimus. For update information on everolimus treatment in breast cancer I have performed a literature search.
I used the keywords "breast cancer" and "everolimus" and extended the search in PubMed from 01/01/2014 to 10/02/2023. I considered all phase 3 trials, the phase 1-2 trials with not repetitive information, studies with biomarker results and I also checked review articles to identify potential relevant other clinical trial reports. I also have made a search in clinicaltrials.gov for recently completed and ongoing trials.
I summarized the search results in this concise and brief report focusing on main trial results and ongoing research with everolimus.
The most promising research directions seem to be further investigations for useable predictive biomarkers, for combinations with other targeted drugs (even in a triple combination) and for the feasibility of pharmacologically guided dosing method.
在激素受体阳性(HR)且人表皮生长因子受体2阴性(HER2)的转移性乳腺癌中,基于内分泌的疗法优于化疗。治疗选择之一是依维莫司与依西美坦或其他内分泌药物联合用于晚期治疗,这主要基于3期BOLERO - 2试验的无进展生存期(PFS)结果。总体而言,临床试验并未证明其能带来总生存期(OS)获益,且相当多的副作用阻碍了其在日常实践中的应用。近年来,细胞周期蛋白依赖性激酶4/6(CDK4/6)抑制剂成为内分泌治疗的首选联合用药伙伴,依维莫司在治疗手段中仍占有一席之地。尽管依维莫司是一种靶向药物,但尚无公认的预测生物标志物,无法进行进一步的患者选择。然而,可以确定几个方向来优化依维莫司的使用。为获取关于依维莫司治疗乳腺癌的最新信息,我进行了文献检索。
我使用关键词“乳腺癌”和“依维莫司”,并在PubMed上将检索时间从2014年1月1日扩展至2023年2月10日。我纳入了所有3期试验、无重复信息的1 - 2期试验、有生物标志物结果的研究,还查阅了综述文章以确定其他潜在相关的临床试验报告。我还在ClinicalTrials.gov上搜索了近期完成和正在进行的试验。
我在这份简明扼要的报告中总结了检索结果,重点关注依维莫司的主要试验结果和正在进行的研究。
最有前景的研究方向似乎是进一步探索可用的预测生物标志物、与其他靶向药物联合使用(甚至三联联合)以及药理指导给药方法的可行性。