GLP-1药物与乳腺癌的影响和安全性

IF 3.1 2区 医学 Q2 ONCOLOGY
Cancer Medicine Pub Date : 2025-06-24 DOI:10.1002/cam4.70932
Kayla Parsons, Mateo Montalvo, Neal Fischbach, Melissa Taylor, Salome Alfaro, Maryam Lustberg
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引用次数: 0

摘要

肥胖症和乳腺癌的发病率在全球范围内呈上升趋势,肥胖症患病率自1990年以来增加了一倍多。到2022年,44%的女性超重,18%的女性肥胖。乳腺癌仍然是女性中最常见的恶性肿瘤,2020年新发病例为220万例。很大一部分乳腺癌患者在诊断时超重或肥胖,这与较高的复发率和死亡率有关。最近,GLP-1受体激动剂(GLP-1 RAs)已成为非常有效的减肥药物。了解肥胖、乳腺癌和减肥之间的关系对于改善患者的治疗效果至关重要。方法采用PubMed、Medline、Web of Science等数据库,对1996 - 2024年的文献进行综合分析。研究包括肥胖和乳腺癌发病率的流行病学数据、系统综述、荟萃分析和乳腺癌患者体重管理干预(行为改变、减肥手术和药物治疗)的临床试验。我们还回顾了有关肥胖和乳腺癌进展的生物学机制的临床前研究。结果流行病学研究一致表明,超重和肥胖的绝经后妇女患乳腺癌的风险增加。诊断时的肥胖与更糟糕的结果有关,包括更高的疾病复发率、乳腺癌特异性死亡率和全因死亡率。治疗期间体重增加,尤其是化疗期间,是很常见的,经常导致肌肉减少性肥胖。行为干预显示出适度的体重减轻,但难以维持。减肥手术降低了患乳腺癌的风险,但缺乏其对肿瘤特征和复发影响的数据。GLP-1受体激动剂,如西马鲁肽和替西帕肽,在非癌症人群中已显示出显著的体重减轻效果,但其在乳腺癌患者中的安全性和有效性尚未得到很好的证实。肥胖在乳腺癌进展中的生物学作用涉及脂肪细胞因子、激素和炎症细胞因子之间复杂的相互作用。减肥干预措施有潜在的好处,但在乳腺癌患者中保持体重减轻是具有挑战性的。新兴的药物治疗,特别是GLP-1受体激动剂,显示出有效控制体重的希望,但需要进一步的研究来确认其安全性和对乳腺癌预后的影响。结论解决乳腺癌患者肥胖问题对改善预后和生活质量至关重要。虽然目前的数据没有显示GLP-1受体激动剂的不良安全信号,但需要更多的研究来充分了解它们的作用。我们迫切需要有效、安全和可持续的体重管理策略来支持乳腺癌患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The Impact and Safety of GLP-1 Agents and Breast Cancer

The Impact and Safety of GLP-1 Agents and Breast Cancer

Introduction

Obesity and breast cancer rates are increasing globally, with obesity prevalence more than doubling since 1990. By 2022, 44% of women were overweight, and 18% were obese. Breast cancer remains the most common malignancy among women, with 2.2 million new cases in 2020. A significant proportion of breast cancer patients are overweight or obese at diagnosis, which is associated with higher recurrence and mortality rates. Recently, GLP-1 receptor agonists (GLP-1 RAs) have emerged as remarkably effective weight loss drugs. Understanding the relationship between obesity, breast cancer, and weight loss is crucial for improving patient outcomes.

Methodology

A comprehensive review of literature from 1996 to 2024 was conducted using databases such as PubMed, Medline, and Web of Science. Studies included epidemiological data on obesity and breast cancer incidence, systematic reviews, meta-analyses, and clinical trials on weight management interventions (behavioral modification, bariatric surgery, and pharmacological treatments) for breast cancer patients. Preclinical studies examining the biological mechanisms linking obesity and breast cancer progression were also reviewed.

Results

Epidemiological studies consistently show that overweight and obese post-menopausal women have an increased risk of developing breast cancer. Obesity at diagnosis is linked to worse outcomes, including higher disease recurrence, breast cancer-specific mortality, and all-cause mortality. Weight gain during treatment, particularly with chemotherapy, is common and often leads to sarcopenic obesity. Behavioral interventions have shown modest weight loss but are difficult to maintain. Bariatric surgery reduces the risk of developing breast cancer but lacks data on its impact on tumor characteristics and recurrence. GLP-1 receptor agonists like semaglutide and tirzepatide have demonstrated significant weight loss in non-cancer populations, but their safety and efficacy in breast cancer patients are not well established.

Discussion

The biology underlying obesity's role in breast cancer progression involves complex interactions between adipocytokines, hormones, and inflammatory cytokines. Weight loss interventions have potential benefits, but sustaining weight reduction in breast cancer patients is challenging. The emerging pharmacological treatments, particularly GLP-1 receptor agonists, show promise for effective weight management but require further investigation to confirm their safety and impact on breast cancer outcomes.

Conclusion

Addressing obesity in breast cancer patients is critical for improving prognosis and quality of life. While current data do not suggest adverse safety signals with GLP-1 receptor agonists, more research is needed to fully understand their effects. Effective, safe, and sustainable weight management strategies are urgently needed to support breast cancer patients.

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来源期刊
Cancer Medicine
Cancer Medicine ONCOLOGY-
CiteScore
5.50
自引率
2.50%
发文量
907
审稿时长
19 weeks
期刊介绍: Cancer Medicine is a peer-reviewed, open access, interdisciplinary journal providing rapid publication of research from global biomedical researchers across the cancer sciences. The journal will consider submissions from all oncologic specialties, including, but not limited to, the following areas: Clinical Cancer Research Translational research ∙ clinical trials ∙ chemotherapy ∙ radiation therapy ∙ surgical therapy ∙ clinical observations ∙ clinical guidelines ∙ genetic consultation ∙ ethical considerations Cancer Biology: Molecular biology ∙ cellular biology ∙ molecular genetics ∙ genomics ∙ immunology ∙ epigenetics ∙ metabolic studies ∙ proteomics ∙ cytopathology ∙ carcinogenesis ∙ drug discovery and delivery. Cancer Prevention: Behavioral science ∙ psychosocial studies ∙ screening ∙ nutrition ∙ epidemiology and prevention ∙ community outreach. Bioinformatics: Gene expressions profiles ∙ gene regulation networks ∙ genome bioinformatics ∙ pathwayanalysis ∙ prognostic biomarkers. Cancer Medicine publishes original research articles, systematic reviews, meta-analyses, and research methods papers, along with invited editorials and commentaries. Original research papers must report well-conducted research with conclusions supported by the data presented in the paper.
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