Real-world experience with trastuzumab deruxtecan in patients with metastatic HER2-positive breast cancer and HER2-positive gastric cancer: A retrospective study

Q4 Medicine
Vladimir I. Evdokimov, Anatoly A. Bloshchinenko, Alexander E. Abolmasov, Alexey A. Vilensky, Michail S. Laskov
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Abstract

Aim. To evaluate the effectiveness of trastuzumab deruxtecan in real-world practice in the Russian Federation. Materials and methods. We performed a retrospective analysis of clinical case series related to the use of trastuzumab deruxtecan (N=15) in the setting of a single clinical center, University Headache Clinic (Dr. Laskov's Clinic), as part of the program for the import of an unapproved drug as a life-saving measure. The overall survival, progression-free survival, and objective response rate were assessed, and individual real-world cases of drug efficacy were presented. Results. Objective response rates are comparable to those shown in large randomized trials. The median follow-up was 67 days; the 6-month overall survival was 70.1% (95% confidence interval [CI] 49.4–99.6%), and the 6-month progression-free survival was 52.1% (95% CI 29.9–90.6%). There were no significant complications associated with therapy; in particular, no events of interstitial lung disease were reported. Discussion. The real-world efficacy of trastuzumab deruxtecan was comparable to that in randomized clinical trials. However, at the level of individual clinical cases, slightly lower efficacy was noted in initially frailer patients (ECOG score 3). Also, it should be noted that the study included patients who had the opportunity to purchase an expensive drug and, therefore, had a social status different from the general population, which could affect the results of this study. Conclusion. The use of trastuzumab deruxtecan in real-world settings has demonstrated high efficacy and a good safety profile.
曲妥珠单抗德鲁西坦治疗转移性 HER2 阳性乳腺癌和 HER2 阳性胃癌患者的实际经验:回顾性研究
的目标。评估曲妥珠单抗德鲁德替康在俄罗斯联邦实际治疗中的有效性。材料和方法。我们回顾性分析了与使用曲妥珠单抗德鲁西替康相关的临床病例系列(N=15),在一个单一的临床中心,大学头痛诊所(拉斯科夫医生诊所),作为未经批准的药物进口计划的一部分,作为拯救生命的措施。评估了总生存期、无进展生存期和客观缓解率,并介绍了实际病例的药物疗效。结果。客观反应率与大型随机试验的结果相当。中位随访时间为67天;6个月总生存率为70.1%(95%可信区间[CI] 49.4-99.6%), 6个月无进展生存率为52.1% (95% CI 29.9-90.6%)。治疗无明显并发症;特别是,没有间质性肺疾病的报道。讨论。曲妥珠单抗德鲁德替康的实际疗效与随机临床试验相当。然而,在个体临床病例的水平上,最初虚弱的患者(ECOG评分为3分)的疗效略低。此外,需要注意的是,该研究包括了有机会购买昂贵药物的患者,因此他们的社会地位与一般人群不同,这可能会影响本研究的结果。结论。曲妥珠单抗deruxtecan在现实环境中的使用已经证明了高疗效和良好的安全性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Modern Oncology
Journal of Modern Oncology Medicine-Oncology
CiteScore
0.50
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0.00%
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审稿时长
5 weeks
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