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戈沙妥珠单抗治疗晚期/转移性非小细胞肺癌的评估。

Evaluation of sacituzumab govitecan for advanced/metastatic non-small cell lung cancer.

作者信息

Cicin Irfan, Karatekin Berivan, Güzelaltuncekic Esra, Kolbas Ilker

机构信息

Medical Faculty, Department of Medical Oncology Oncology, Istinye University, Istanbul, Turkey.

Medical Park Florya Hospital, Department of Pulmonology, Istanbul Aydin University, Istanbul, Turkey.

出版信息

Expert Rev Anticancer Ther. 2025 Aug;25(8):845-852. doi: 10.1080/14737140.2025.2515989. Epub 2025 Jun 5.

Abstract

INTRODUCTION

Non-small cell lung cancer (NSCLC) remains the leading cause of cancer-related mortality worldwide. Despite advancements in targeted therapies and immune checkpoint inhibitors, many patients with advanced NSCLC experience disease progression, necessitating novel therapeutic approaches like antibody-drug conjugate (ADC).

AREAS COVERED

Sacituzumab govitecan, a trophoblast cell surface antigen 2 (Trop-2) - directed ADC, has emerged as a potential treatment for advanced NSCLC This review evaluates its mechanism of action, clinical efficacy, safety profile, and potential in combination therapies, particularly in heavily pretreated patients. A literature search was conducted using PubMed with keywords 'sacituzumab govitecan' and 'lung cancer,' incorporating relevant studies, including the EVOKE-01 trial.

EXPERT OPINION

Sacituzumab govitecan offers a promising alternative for patients unresponsive to conventional treatments. While it demonstrates encouraging response rates and manageable toxicity, further research is needed to refine patient selection and optimize combination strategies. Ongoing trials, such as KEYNOTE-D46/EVOKE-3 May 2001define its role in first-line NSCLC treatment.

摘要

引言

非小细胞肺癌(NSCLC)仍然是全球癌症相关死亡的主要原因。尽管靶向治疗和免疫检查点抑制剂取得了进展,但许多晚期NSCLC患者仍经历疾病进展,因此需要抗体药物偶联物(ADC)等新型治疗方法。

涵盖领域

戈沙妥珠单抗是一种靶向滋养层细胞表面抗原2(Trop-2)的ADC,已成为晚期NSCLC的一种潜在治疗方法。本综述评估了其作用机制、临床疗效、安全性以及在联合治疗中的潜力,特别是在经过大量治疗的患者中。使用PubMed以“戈沙妥珠单抗”和“肺癌”为关键词进行了文献检索,纳入了相关研究,包括EVOKE-01试验。

专家意见

戈沙妥珠单抗为对传统治疗无反应的患者提供了一个有前景的替代方案。虽然它显示出令人鼓舞的缓解率和可管理的毒性,但仍需要进一步研究以优化患者选择和联合策略。正在进行的试验,如KEYNOTE-D46/EVOKE-3(2001年5月),将确定其在一线NSCLC治疗中的作用。

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