Morga Antonia, Shiozawa Aki, Todorova Lora, Ajmera Mayank, Arregui Maria, Wissinger Erika
Astellas Pharma Europe Ltd., Addlestone KT15 2NX, UK.
Astellas Pharma US, Inc., Northbrook, IL 60062, USA.
J Clin Med. 2025 Apr 10;14(8):2601. doi: 10.3390/jcm14082601.
This systematic literature review (SLR) evaluates the global burden of treatment-induced vasomotor symptoms (VMSs) in individuals with breast cancer receiving tamoxifen or aromatase inhibitors (AIs). Embase and PubMed were searched for observational and interventional studies published between January 2010 and January 2023 reporting on adults who experienced moderate to severe VMSs after tamoxifen or AI treatment for breast cancer. Epidemiological, clinical, humanistic, economic, and treatment pattern data were extracted where available. Of 694 unique publications identified, 37 independent studies (22 observational and 15 interventional) were included. The prevalence or incidence of treatment-induced VMSs was reported in 17 studies. The prevalence of hot flashes ranged from 32.5% to 82.9% in observational studies, while their incidence ranged from 2% to 60.0% in interventional studies. In four studies that reported data, individuals experienced VMSs with a frequency of 2 to 20 episodes per day. There were limited data on VMS timing (within a 24 h period or in relation to treatment dosing), duration, and correlations with clinical outcomes. Age, weight gain, body mass index, ethnicity, employment intensity, and certain genetic haplotypes were identified as risk factors for VMSs; however, these factors were often reported in only one study each. Notable evidence gaps in the literature included treatment options or management strategies for treatment-induced VMSs and the economic burden associated with treatment-induced VMSs. This SLR highlights the burden of treatment-induced VMSs in individuals with breast cancer receiving tamoxifen or AI therapy. Moderate to severe symptoms were reported in a large proportion of individuals across several studies. Evidence gaps were identified for economic burden and treatment patterns; further research is needed to understand the unmet needs for this population.
本系统文献综述(SLR)评估了接受他莫昔芬或芳香化酶抑制剂(AI)治疗的乳腺癌患者中治疗引起的血管舒缩症状(VMS)的全球负担。在Embase和PubMed数据库中检索了2010年1月至2023年1月发表的观察性和干预性研究,这些研究报告了成年乳腺癌患者在接受他莫昔芬或AI治疗后出现中度至重度VMS的情况。如有可用数据,提取了流行病学、临床、人文、经济和治疗模式数据。在识别出的694篇独特出版物中,纳入了37项独立研究(22项观察性研究和15项干预性研究)。17项研究报告了治疗引起的VMS的患病率或发病率。观察性研究中潮热的患病率为32.5%至82.9%,而干预性研究中其发病率为2%至60.0%。在四项报告数据的研究中,个体经历VMS的频率为每天2至20次发作。关于VMS发作时间(24小时内或与治疗给药相关)、持续时间以及与临床结局的相关性的数据有限。年龄、体重增加、体重指数、种族、工作强度和某些基因单倍型被确定为VMS的风险因素;然而,这些因素通常每项研究仅报告一次。文献中明显的证据空白包括治疗引起的VMS的治疗选择或管理策略以及与治疗引起的VMS相关的经济负担。本SLR强调了接受他莫昔芬或AI治疗的乳腺癌患者中治疗引起的VMS的负担。多项研究报告了很大一部分个体出现中度至重度症状。确定了经济负担和治疗模式方面的证据空白;需要进一步研究以了解该人群未满足的需求。