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曲妥珠单抗-德鲁替康在乳腺癌脑转移中的临床前和临床疗效。

Preclinical and Clinical Efficacy of Trastuzumab Deruxtecan in Breast Cancer Brain Metastases.

机构信息

Dana-Farber Cancer Institute, Boston, Massachusetts.

Duke Cancer Institute, Durham, North Carolina.

出版信息

Clin Cancer Res. 2023 Jan 4;29(1):174-182. doi: 10.1158/1078-0432.CCR-22-1138.

Abstract

PURPOSE

Brain metastases can occur in up to 50% of patients with metastatic HER2-positive breast cancer. Because patients with active brain metastases were excluded from previous pivotal clinical trials, the central nervous system (CNS) activity of the antibody-drug conjugate trastuzumab deruxtecan (T-DXd) is not well characterized.

EXPERIMENTAL DESIGN

We studied how T-DXd affects growth and overall survival in orthotopic patient-derived xenografts (PDX) of HER2-positive and HER2-low breast cancer brain metastases (BCBM). Separately, we evaluated the effects of T-DXd in a retrospective cohort study of 17 patients with stable or active brain metastases.

RESULTS

T-DXd inhibited tumor growth and prolonged survival in orthotopic PDX models of HER2-positive (IHC 3+) and HER2-low (IHC 2+/FISH ratio < 2) BCBMs. T-DXd reduced tumor size and prolonged survival in a T-DM1-resistant HER2-positive BCBM PDX model. In a retrospective multi-institutional cohort study of 17 patients with predominantly HER2-positive BCBMs, the CNS objective response rate (ORR) was 73% (11/15) while extracranial response rate was 45% (5/11). In the subset of patients with untreated or progressive BCBM at baseline, the CNS ORR was 70% (7/10). The median time on treatment with T-DXd was 8.9 (1.3-16.2) months, with 42% (7/17) remaining on treatment at data cutoff.

CONCLUSIONS

T-DXd demonstrates evidence of CNS activity in HER2-positive and HER2-low PDX models of BCBM and preliminary evidence of clinical efficacy in a multi-institution case series of patients with BCBM. Prospective clinical trials to further evaluate CNS activity of T-DXd in patients with active brain metastases are warranted. See related commentary by Soffietti and Pellerino, p. 8.

摘要

目的

多达 50%的转移性 HER2 阳性乳腺癌患者会发生脑转移。由于先前的关键性临床试验排除了有活动性脑转移的患者,因此抗体药物偶联物 trastuzumab deruxtecan(T-DXd)的中枢神经系统(CNS)活性尚未得到充分描述。

实验设计

我们研究了 T-DXd 如何影响 HER2 阳性和 HER2 低表达乳腺癌脑转移(BCBM)的原位患者来源异种移植(PDX)的生长和总生存期。此外,我们还在一项 17 例有稳定或活动性脑转移的患者回顾性队列研究中评估了 T-DXd 的作用。

结果

T-DXd 抑制了 HER2 阳性(IHC 3+)和 HER2 低表达(IHC 2+/FISH 比值<2)BCBM 原位 PDX 模型中的肿瘤生长并延长了生存期。在 T-DM1 耐药的 HER2 阳性 BCBM PDX 模型中,T-DXd 缩小了肿瘤体积并延长了生存期。在一项包含 17 例主要为 HER2 阳性 BCBM 患者的多机构回顾性队列研究中,CNS 客观缓解率(ORR)为 73%(11/15),而颅外缓解率为 45%(5/11)。在基线时有未经治疗或进展性 BCBM 的患者亚组中,CNS ORR 为 70%(7/10)。T-DXd 的中位治疗时间为 8.9(1.3-16.2)个月,数据截止时 42%(7/17)的患者仍在接受治疗。

结论

T-DXd 在 HER2 阳性和 HER2 低表达 BCBM 的 PDX 模型中显示出 CNS 活性的证据,并在一项多机构 BCBM 患者病例系列研究中初步证实了临床疗效。需要进行前瞻性临床试验,以进一步评估 T-DXd 在有活动性脑转移的患者中的 CNS 活性。见 Soffietti 和 Pellerino 的相关评论,第 8 页。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be7e/9811155/b345d0b86db6/174fig1.jpg

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