1级间质性肺疾病/肺炎恢复后再治疗曲妥珠单抗德鲁德替康的汇总分析

IF 65.4 1区 医学 Q1 ONCOLOGY
H S Rugo, E Tokunaga, H Iwata, V Petry, E F Smit, Y Goto, D-W Kim, K Shitara, J F Gruden, S Modi, J Cortés, I Krop, P A Jänne, Y Cheng, C Taitt, F-C Cheng, C A Powell
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引用次数: 0

摘要

目的:曲妥珠单抗德鲁西替康(T-DXd)是一种抗体-药物结合治疗多发性实体瘤的药物,具有间质性肺疾病/肺炎(ILD)的风险。管理指南通常要求中断1级ILD的T-DXd治疗,并在影像学结果明确后可能重新治疗。该合并分析检查了T-DXd再治疗时间和1级ILD恢复后的ILD复发率。患者和方法:数据来自9项临床试验,这些患者采用T-DXd (5.4-8.0 mg/kg)治疗各种HER2阳性、HER2低或HER2 (ERBB2)突变的实体瘤。ILD事件由调查人员报告和分级,并由独立的ILD裁决委员会确认为与药物有关。从首次研究者评估的1级和裁决委员会确认的药物相关ILD事件(ILD1)中恢复的患者可以接受T-DXd再治疗。对患者进行评估,直至疾病进展或数据截止。结果:在2145例合并患者中,9%(193/2145)为1级ILD1,其中23.3%(45/193)接受T-DXd治疗。中位再治疗持续时间为85天(范围1-848天);17.8%(8/45)的患者接受T-DXd再治疗≥1年。复发率为33.3% (15/45);从T-DXd再治疗到ILD2的中位时间为64天(范围,22-391),是低级别事件(1级,n=6;2级,n=9;无3级以上或致命事件)。停止T-DXd再治疗的原因为疾病进展(33.3% [15/45]);ILD复发(20% [9/45]);非ild不良事件(17.8% [8/45]);医生的决定(4.4%[2/45])。在分析截止时,24.4%(11/45)的患者仍在接受治疗,大多数ILD2患者(60%[9/15])已康复,无或无后遗症。结论:这是第一次大规模的汇总分析,证明了T-DXd在1级ILD恢复后再治疗的安全性。三分之一的患者出现ILD复发;所有复发事件均为1/2级,使用现有治疗指南可控制。在1级药物相关性ILD消退后再治疗T-DXd有可能使治疗获益最大化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pooled analysis of trastuzumab deruxtecan retreatment after recovery from grade 1 interstitial lung disease/pneumonitis.

Background: Trastuzumab deruxtecan (T-DXd), an antibody-drug conjugate treatment for multiple solid tumors, carries risk of interstitial lung disease/pneumonitis (ILD). Management guidelines generally mandate interrupting T-DXd treatment for grade 1 ILD, with possible retreatment following resolution of imaging findings. This pooled analysis examined T-DXd retreatment duration and ILD recurrence following recovery from grade 1 ILD.

Patients and methods: Data were pooled from nine clinical trials of patients with various human epidermal growth factor receptor 2 (HER2)-positive, HER2-low, or HER2 (ERBB2)-mutant solid tumors treated with T-DXd (5.4-8.0 mg/kg). ILD events were reported and graded by investigators and confirmed as drug related by an independent ILD adjudication committee. Patients who recovered from a first investigator-assessed grade 1 and adjudication committee-confirmed drug-related ILD event (ILD1) could receive T-DXd retreatment. Patients were evaluated until disease progression or data cut-off.

Results: Among 2145 pooled patients, 9% (193/2145) had grade 1 ILD1, of which 23.3% (45/193) were retreated with T-DXd. Median retreatment duration was 85 days (range 1-848 days); 17.8% (8/45) of patients received T-DXd retreatment for ≥1 year. ILD recurrence (ILD2) occurred in 33.3% (15/45) of retreated patients; median time to ILD2 from T-DXd retreatment was 64 days (range, 22-391 days) and were low-grade events (grade 1, n = 6; grade 2, n = 9; no grade ≥3 or fatal events). Reasons for T-DXd retreatment discontinuation were disease progression [33.3% (15/45)]; ILD recurrence [20% (9/45)]; non-ILD adverse events [17.8% (8/45)]; and physician's decision [4.4% (2/45)]. At the analysis cut-off, 24.4% (11/45) of retreated patients were still receiving treatment, and most patients with ILD2 [60% (9/15)] had recovered with/without sequelae.

Conclusions: This first large-scale pooled analysis demonstrates the safety of T-DXd retreatment after recovery from grade 1 ILD. ILD recurred in one-third of patients; all recurrence events were grade 1/2 and manageable using existing treatment guidelines. T-DXd retreatment following resolution of grade 1 drug-related ILD has potential to maximize therapeutic benefit.

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来源期刊
Annals of Oncology
Annals of Oncology 医学-肿瘤学
CiteScore
63.90
自引率
1.00%
发文量
3712
审稿时长
2-3 weeks
期刊介绍: Annals of Oncology, the official journal of the European Society for Medical Oncology and the Japanese Society of Medical Oncology, offers rapid and efficient peer-reviewed publications on innovative cancer treatments and translational research in oncology and precision medicine. The journal primarily focuses on areas such as systemic anticancer therapy, with a specific emphasis on molecular targeted agents and new immune therapies. We also welcome randomized trials, including negative results, as well as top-level guidelines. Additionally, we encourage submissions in emerging fields that are crucial to personalized medicine, such as molecular pathology, bioinformatics, modern statistics, and biotechnologies. Manuscripts related to radiotherapy, surgery, and pediatrics will be considered if they demonstrate a clear interaction with any of the aforementioned fields or if they present groundbreaking findings. Our international editorial board comprises renowned experts who are leaders in their respective fields. Through Annals of Oncology, we strive to provide the most effective communication on the dynamic and ever-evolving global oncology landscape.
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