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在真实世界临床环境中评估相对剂量强度对曲妥珠单抗德鲁昔单抗治疗转移性乳腺癌疗效的影响。

Evaluating the impact of relative dose intensity on efficacy of trastuzumab deruxtecan for metastatic breast cancer in the real-world clinical setting.

作者信息

Lee Han Yi, Shih Vivianne, Chan Jack Junjie, Liong Shun Zi, Tan Ryan Shea Ying Cong, Ma Jun, Chua Bernard Ji Guang, Tan Joshua Zhi Chien, Lee Chuan Yaw, Teo Wei Ling, Tan Su-Ming, Nitar Phyu, Yap Yoon Sim, Wong Mabel, Dent Rebecca, Wong Fuh Yong, Tan Tira J

机构信息

Division of Medical Oncology, National Cancer Centre Singapore, Singapore.

Department of Pharmacy, National Cancer Centre Singapore, Singapore.

出版信息

Ann Acad Med Singap. 2025 Aug 6;54(8):458-466. doi: 10.47102/annals-acadmedsg.202576.

Abstract

INTRODUCTION

Trastuzumab deruxtecan (T-DXd) has revolutionised treatment for metastatic breast cancer (MBC). While effective, its high cost and toxicities, such as fatigue and nausea, pose challenges.

METHOD

Medical records from the Joint Breast Cancer Registry in Singapore were used to study MBC patients treated with T-DXd (February 2021-June 2024). This study was conducted to address whether reducing dose intensity and density may have an adverse effect on treatment outcomes.

RESULTS

Eighty-seven MBC patients were treated with T-DXd, with a median age of 59 years. At the time of data cutoff, 32.1% of patients were still receiving T-DXd. Over half (54%) of the patients received treatment with an initial relative dose intensity (RDI) of <;85%. Overall median real-world progression-free survival (rwPFS) was 8.1 months. rwPFS was similar between RDI groups (<85%: 8.7 months, <85%: 8.1 months, P=0.62). However, human epidermal growth receptor 2 (HER2)-positive patients showed significantly better rwPFS outcomes compared to HER2-low patients (8.8 versus 2.5 months, P<0.001). Only 16% with central nervous system (CNS) involvement had CNS progressive disease on treatment. No significant progression-free survival (PFS) differences were found between patients with or without CNS disease, regardless of RDI groups. Five patients (5.7%) developed interstitial lung disease (ILD), with 3 (3.4%) having grade 3 events. Two required high-dose steroids and none were rechallenged after ILD. There were no fatalities.

CONCLUSION

Our study demonstrated that reduced dose intensity and density had no significant impact on rwPFS or treatment-related toxicities. Furthermore, only 5.7% of patients developed ILD. T-Dxd provided good control of CNS disease, with 82% of patients achieving CNS disease control.

摘要

引言

曲妥珠单抗德鲁昔单抗(T-DXd)彻底改变了转移性乳腺癌(MBC)的治疗方式。虽然它有效,但高昂的成本以及疲劳和恶心等毒性反应带来了挑战。

方法

利用新加坡联合乳腺癌登记处的医疗记录研究接受T-DXd治疗的MBC患者(2021年2月至2024年6月)。开展这项研究是为了探讨降低剂量强度和密度是否会对治疗结果产生不利影响。

结果

87例MBC患者接受了T-DXd治疗,中位年龄为59岁。在数据截止时,32.1%的患者仍在接受T-DXd治疗。超过半数(54%)的患者初始相对剂量强度(RDI)<85%时接受治疗。总体中位真实世界无进展生存期(rwPFS)为8.1个月。RDI组之间的rwPFS相似(<85%:8.7个月,<85%:8.1个月,P=0.62)。然而,与HER2低表达患者相比,人表皮生长因子受体2(HER2)阳性患者的rwPFS结果显著更好(8.8个月对2.5个月,P<0.001)。仅16%有中枢神经系统(CNS)受累的患者在治疗时出现CNS进展性疾病。无论RDI组如何,有或无CNS疾病的患者之间未发现显著的无进展生存期(PFS)差异。5例患者(5.7%)发生间质性肺疾病(ILD),其中3例(3.4%)为3级事件。2例需要高剂量类固醇治疗,ILD后均未再次接受治疗。无死亡病例。

结论

我们的研究表明,降低剂量强度和密度对rwPFS或治疗相关毒性无显著影响。此外,仅5.7%的患者发生ILD。T-DXd对CNS疾病提供了良好的控制,82%的患者实现了CNS疾病控制。

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