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曲妥珠单抗德鲁替康作为一种不依赖组织类型的药物的潜力。

The Potential of Trastuzumab Deruxtecan as a Tissue Agnostic Drug.

作者信息

Jørgensen Jan Trøst

机构信息

Medical Science, Dx-Rx Institute, Fredensborg, Denmark.

出版信息

Oncology. 2023;101(12):836-842. doi: 10.1159/000533866. Epub 2023 Aug 31.

Abstract

BACKGROUND

Many modern anticancer drugs are designed to target specific molecular alterations harbored by the cancer. If a specific drug is able to target these alterations, regardless of the organ or tissue in which the cancer originates, it will often be characterized as a tissue- or tumor agnostic drug. According to the Food and Drug Administration (FDA), a tissue-agnostic drug refers to a drug that targets a specific molecular alteration across multiple cancer types, as defined by organ, tissue, or tumor type.

SUMMARY

Over the last 6 years, the FDA has approved seven tissue-agnostic drugs, and more are anticipated in the future. One promising candidate for a tissue-agnostic classification is the antibody-drug conjugate trastuzumab deruxtecan (T-DXd). Currently, T-DXd is approved for the treatment of human epidermal growth factor receptor 2 (HER2)-positive and HER2-low breast cancer, HER2-positive gastric or gastroesophageal junction adenocarcinoma, and non-small cell lung cancer with activating HER2 mutations. Ongoing clinical research is exploring the potential of T-DXd in various solid tumors that harbor specific HER2 molecular alterations, and encouraging results, including the interim data from the DESTINY-PanTumor02 trial, have been published, which suggest a tissue-agnostic potential.

KEY MESSAGES

Published phase I data as well as the interim results from the phase II DESTINY-PanTumor02 trial indicates that patients with different HER2-positive advanced solid tumors may benefit from treatment with T-DXd. Based on the currently available data, it seems likely that T-DXd possesses pantumor activity. However, different clinical trials are ongoing, and it will be necessary to see the results from these trials before drawing a final conclusion. When discussing tissue-agnostic potential, it is important to add that for most of the patients enrolled in the DESTINY-PanTumor02 and other trials, few treatment alternatives seem to exist, and T-DXd might be able to cover an unmet medical need.

摘要

背景

许多现代抗癌药物旨在靶向癌症所具有的特定分子改变。如果一种特定药物能够靶向这些改变,无论癌症起源于哪个器官或组织,它通常会被归类为组织或肿瘤非特异性药物。根据美国食品药品监督管理局(FDA)的定义,组织非特异性药物是指一种针对多种癌症类型中特定分子改变的药物,这些癌症类型由器官、组织或肿瘤类型来界定。

总结

在过去6年中,FDA已批准了7种组织非特异性药物,预计未来还会有更多。抗体药物偶联物曲妥珠单抗德曲妥珠单抗(T-DXd)是一种有望获得组织非特异性分类的药物。目前,T-DXd已被批准用于治疗人表皮生长因子受体2(HER2)阳性和HER2低表达乳腺癌、HER2阳性胃癌或胃食管交界腺癌,以及具有HER2激活突变的非小细胞肺癌。正在进行的临床研究正在探索T-DXd在各种具有特定HER2分子改变的实体瘤中的潜力,并且已经公布了令人鼓舞的结果,包括DESTINY-PanTumor02试验的中期数据,这些结果表明其具有组织非特异性潜力。

关键信息

已发表的I期数据以及II期DESTINY-PanTumor02试验的中期结果表明,不同的HER2阳性晚期实体瘤患者可能从T-DXd治疗中获益。根据目前可得的数据,T-DXd似乎具有泛肿瘤活性。然而,不同的临床试验正在进行,在得出最终结论之前有必要查看这些试验的结果。在讨论组织非特异性潜力时,需要补充的是,对于参与DESTINY-PanTumor02和其他试验的大多数患者来说,似乎几乎没有其他治疗选择,而T-DXd可能能够满足未被满足的医疗需求。

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