Therapeutic Potential of Datopotamab Deruxtecan in the Treatment of Advanced Non-Small Cell Lung Cancer: Evidence to Date.

IF 2.8 4区 医学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
OncoTargets and therapy Pub Date : 2025-04-23 eCollection Date: 2025-01-01 DOI:10.2147/OTT.S466220
Maya Gogtay, Nikhila Aimalla, Ram Prakash Thirugnanasambandam, Apar Kishor Ganti
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引用次数: 0

Abstract

Lung cancer is the leading cause of global cancer mortality, accounting for an estimated 2 million diagnoses and 1.8 million deaths annually. Treatment choices for non-small cell lung cancer include surgery, radiation therapy, chemotherapy, immunotherapy, or molecularly targeted therapy. Antibody-drug conjugates (ADCs), often likened to "biological missiles", are rapidly evolving as a targeted therapeutic approach. Trophoblast cell surface antigen 2 (Trop 2) is a 36-kDa cell surface glycoprotein, which is expressed in various cancers. This fuels oncogenic signaling pathways, driving tumor advancement, invasion, and spread. Its limited expression in healthy human tissues underscores its potential as a target for cancer treatment. Datopotamab Deruxtecan (Dato-Dxd) is an investigational ADC that targets Trop-2. This review discusses the current treatment landscape involving therapy with Dato-Dxd for advanced NSCLC. Dato-DXd was first used in metastatic solid tumors in the Phase I TROPION-PanTumor 01 trial, which showed promising antitumor activity in the previously pretreated NSCLC cohort and a manageable safety outline. In TROPION-Lung01, Dato-DXD was studied in metastatic NSCLC patients who were previously treated and showed an objective response rate of 26.4% (Dato-DXd). Other trials, including TROPION PanTumor 02, ICARUS - Lung 01, and TROPION Lung 05, showed comparable results. Dato-DXd used along with pembrolizumab, with or without systemic chemotherapy, in TROPION Lung 02 with promising efficacy results. The most common any-grade treatment-emergent adverse events were stomatitis, nausea, and hair loss, mostly grade 1-2. There are several clinical trials in the pipeline using Dato-DXd in the front-line metastatic setting and resectable NSCLC patients. Dato-DXd is currently pending approval from the US Food and Drug Administration (FDA). If approved, datopotamab deruxtecan will be the first TROP2-directed antibody-drug conjugate for non-small cell lung cancer.

Datopotamab Deruxtecan治疗晚期非小细胞肺癌的潜力:迄今为止的证据。
肺癌是全球癌症死亡的主要原因,估计每年有200万例诊断和180万例死亡。非小细胞肺癌的治疗选择包括手术、放射治疗、化疗、免疫治疗或分子靶向治疗。抗体-药物偶联物(adc)通常被比作“生物导弹”,作为一种靶向治疗方法正在迅速发展。滋养细胞表面抗原2 (Trop 2)是一种36kda的细胞表面糖蛋白,在多种癌症中表达。这刺激了致癌信号通路,驱动肿瘤的进展、侵袭和扩散。它在健康人体组织中的有限表达强调了它作为癌症治疗靶点的潜力。Datopotamab Deruxtecan (Dato-Dxd)是一种针对Trop-2的研究性ADC。这篇综述讨论了目前Dato-Dxd治疗晚期NSCLC的治疗情况。Dato-DXd在I期TROPION-PanTumor 01试验中首次用于转移性实体瘤,该试验在先前预处理的NSCLC队列中显示出有希望的抗肿瘤活性和可管理的安全性轮廓。在TROPION-Lung01中,Dato-DXD在先前接受过治疗的转移性NSCLC患者中进行了研究,客观缓解率为26.4% (Dato-DXD)。其他试验,包括TROPION pantum02、ICARUS - Lung 01和TROPION Lung 05,也显示了类似的结果。Dato-DXd与派姆单抗(pembrolizumab)联合使用,伴或不伴全身化疗,在TROPION Lung 02中具有良好的疗效结果。最常见的任何级别治疗出现的不良事件是口腔炎,恶心和脱发,主要是1-2级。Dato-DXd在一线转移性和可切除的非小细胞肺癌患者中的临床试验正在进行中。Dato-DXd目前正在等待美国食品和药物管理局(FDA)的批准。如果获得批准,datopotamab deruxtecan将成为首个针对非小细胞肺癌的trop2靶向抗体-药物偶联物。
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来源期刊
OncoTargets and therapy
OncoTargets and therapy BIOTECHNOLOGY & APPLIED MICROBIOLOGY-ONCOLOGY
CiteScore
9.70
自引率
0.00%
发文量
221
审稿时长
1 months
期刊介绍: OncoTargets and Therapy is an international, peer-reviewed journal focusing on molecular aspects of cancer research, that is, the molecular diagnosis of and targeted molecular or precision therapy for all types of cancer. The journal is characterized by the rapid reporting of high-quality original research, basic science, reviews and evaluations, expert opinion and commentary that shed novel insight on a cancer or cancer subtype. Specific topics covered by the journal include: -Novel therapeutic targets and innovative agents -Novel therapeutic regimens for improved benefit and/or decreased side effects -Early stage clinical trials Further considerations when submitting to OncoTargets and Therapy: -Studies containing in vivo animal model data will be considered favorably. -Tissue microarray analyses will not be considered except in cases where they are supported by comprehensive biological studies involving multiple cell lines. -Biomarker association studies will be considered only when validated by comprehensive in vitro data and analysis of human tissue samples. -Studies utilizing publicly available data (e.g. GWAS/TCGA/GEO etc.) should add to the body of knowledge about a specific disease or relevant phenotype and must be validated using the authors’ own data through replication in an independent sample set and functional follow-up. -Bioinformatics studies must be validated using the authors’ own data through replication in an independent sample set and functional follow-up. -Single nucleotide polymorphism (SNP) studies will not be considered.
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