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泽尼达妥单抗在HER2阳性晚期胆管癌患者中的真实世界疗效。

Real-world efficacy of zanidatamab in patients with HER2 positive advanced biliary tract cancers.

作者信息

Smolenschi Cristina, Blanc Jean-Frédéric, Lancry Anna, Klajer Elodie, Debaillon-Vesque Audrey, Vantelon Jean Marie, Boileve Alice, Valery Marine, Hollebecque Antoine, Ducreux Michel, Decraecker Marie

机构信息

Medical Oncology Department, Gustave Roussy, Villejuif, France; Drug Development Department, Gustave Roussy, Villejuif, France.

Oncology Unit, Hôpital Haut Lévêque, CIC 1401, Bordeaux University Hospital, Pessac 33604, France.

出版信息

Eur J Cancer. 2025 Jun 3;222:115432. doi: 10.1016/j.ejca.2025.115432. Epub 2025 Apr 18.

Abstract

INTRODUCTION

In the HERIZON BTC 01 trial for patients with HER2-positive biliary tract cancer (BTC) previously treated with systemic therapy, zanidatamab improved the objective response rate, disease control rate (DCR), progression-free survival (PFS), and overall survival (OS). However, real-world data are needed to assess its efficacy and safety outside clinical trials.

PATIENTS & METHODS: We conducted an investigator initiated national multicenter retrospective study of most patients with BTC treated with zanidatamab in France as part of a compassionate access. The primary endpoint was PFS.

RESULTS

Our study included 20 patients with metastatic BTC enrolled between September 2022 and November 2024. The median age at diagnosis was 61.5 (interquartile range: 55-69) years and the majority of patients had gallbladder cancer (n = 12, 60 %). After a median follow-up of 8.5 (95 % confidence interval [CI]: 3.3-11.8) months, the median PFS was 6.7 (95 % CI 1.3-11.8) months, with an estimated OS at 1 year of 79.1 % (95 % CI: 53.2-91.6 %). The DCR was 65 %, with 40 % confirmed partial responses and a median duration of response of 7.3 (95 % CI: 2.06-16) months. Patients with immunohistochemistry (IHC) 3 + HER2 scores had a better PFS [8 (95 % CI: 1.5-18.4) months] than those with 2 + HER2 scores obtained by IHC followed by fluorescence in situ hybridization amplification or next-generation sequencing [1.4 (95 % CI: 1.1-6.8) months] (P = 0.02). No statistical difference in 1-year estimated OS rates was observed (P = 0.39). There were no grade 3 or 4 treatment-related adverse events or cardiac toxicities.

CONCLUSION

The benefits of in patients with HER2-positive BTC were confirmed. Zanidatamab should be considered for patients with this condition.

摘要

引言

在HERIZON BTC 01试验中,对于先前接受过全身治疗的HER2阳性胆管癌(BTC)患者,zanidatamab提高了客观缓解率、疾病控制率(DCR)、无进展生存期(PFS)和总生存期(OS)。然而,需要真实世界的数据来评估其在临床试验之外的疗效和安全性。

患者与方法

我们开展了一项由研究者发起的全国多中心回顾性研究,纳入了法国大多数接受zanidatamab治疗的BTC患者,作为同情用药的一部分。主要终点是PFS。

结果

我们的研究纳入了2022年9月至2024年11月期间登记的20例转移性BTC患者。诊断时的中位年龄为61.5岁(四分位间距:55 - 69岁),大多数患者患有胆囊癌(n = 12,60%)。中位随访8.5个月(95%置信区间[CI]:3.3 - 11.8)后,中位PFS为6.7个月(95% CI 1.3 - 11.8),1年时的估计OS为79.1%(95% CI:53.2 - 91.6%)。DCR为65%,40%为确认的部分缓解,中位缓解持续时间为7.3个月(95% CI:2.06 - 16)。免疫组化(IHC)3 + HER2评分的患者的PFS[8个月(95% CI:1.5 - 18.4)]优于通过IHC继以荧光原位杂交扩增或二代测序获得2 + HER2评分的患者[1.4个月(95% CI:1.1 - 6.8)](P = 0.02)。1年估计OS率未观察到统计学差异(P = 0.39)。没有3级或4级治疗相关不良事件或心脏毒性。

结论

HER2阳性BTC患者使用zanidatamab的获益得到了证实。对于这种情况的患者应考虑使用zanidatamab。

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