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与拓扑替康相比,罗伐匹妥珠单抗替西瑞林作为DLL3高表达小细胞肺癌二线治疗的疗效和安全性:3期TAHOE研究结果

Efficacy and Safety of Rovalpituzumab Tesirine Compared With Topotecan as Second-Line Therapy in DLL3-High SCLC: Results From the Phase 3 TAHOE Study.

作者信息

Blackhall Fiona, Jao Kevin, Greillier Laurent, Cho Byoung Chul, Penkov Konstantin, Reguart Noemi, Majem Margarita, Nackaerts Kristiaan, Syrigos Konstantinos, Hansen Karin, Schuette Wolfgang, Cetnar Jeremy, Cappuzzo Federico, Okamoto Isamu, Erman Mustafa, Langer Seppo W, Kato Terufumi, Groen Harry, Sun Zhaowen, Luo Yan, Tanwani Poonam, Caffrey Laura, Komarnitsky Philip, Reinmuth Niels

机构信息

Division of Cancer Sciences, The University of Manchester, Manchester, United Kingdom; Department of Medical Oncology, The Christie National Health Service (NHS) Foundation Trust, Manchester, United Kingdom.

Department of Hematology and Oncology, Hopital du Sacre Coeur Montreal, Montreal, Canada.

出版信息

J Thorac Oncol. 2021 Sep;16(9):1547-1558. doi: 10.1016/j.jtho.2021.02.009. Epub 2021 Feb 16.

Abstract

INTRODUCTION

DLL3, an atypical Notch ligand, is expressed in SCLC tumors but is not detectable in normal adult tissues. Rovalpituzumab tesirine (Rova-T) is an antibody-drug conjugate containing a DLL3-targeting antibody tethered to a cytotoxic agent pyrrolobenzodiazepine by means of a protease-cleavable linker. The efficacy and safety of Rova-T compared with topotecan as second-line therapy in patients with SCLC expressing high levels of DLL3 (DLL3-high) was evaluated.

METHODS

The TAHOE study was an open-label, two-to-one randomized, phase 3 study comparing Rova-T with topotecan as second-line therapy in DLL3-high advanced or metastatic SCLC. Rova-T (0.3 mg/kg) was administered intravenously on day 1 of a 42-day cycle for two cycles, with two additional cycles available to patients who met protocol-defined criteria for continued dosing. Topotecan (1.5 mg/m) was administered intravenously on days 1 to 5 of a 21-day cycle. The primary end point was overall survival (OS).

RESULTS

Patients randomized to Rova-T (n = 296) and topotecan (n = 148) were included in the efficacy analyses. The median age was 64 years, and 77% had the extensive disease at initial diagnosis. The median OS (95% confidence interval) was 6.3 months (5.6-7.3) in the Rova-T arm and 8.6 months (7.7-10.1) in the topotecan arm (hazard ratio, 1.46 [95% confidence interval: 1.17-1.82]). An independent data monitoring committee recommended that enrollment be discontinued because of the shorter OS observed with Rova-T compared with topotecan. Safety profiles for both drugs were consistent with previous reports.

CONCLUSIONS

Compared with topotecan, which is the current standard second-line chemotherapy, Rova-T exhibited an inferior OS and higher rates of serosal effusions, photosensitivity reaction, and peripheral edema in patients with SCLC. A considerable unmet therapeutic need remains in this population.

摘要

引言

DLL3是一种非典型的Notch配体,在小细胞肺癌(SCLC)肿瘤中表达,但在正常成人组织中无法检测到。罗伐匹妥珠单抗替西瑞林(Rova-T)是一种抗体药物偶联物,包含一种靶向DLL3的抗体,通过可被蛋白酶切割的连接子与细胞毒性药物吡咯并苯二氮䓬相连。评估了Rova-T与拓扑替康作为二线治疗方案在高表达DLL3(DLL3高表达)的SCLC患者中的疗效和安全性。

方法

TAHOE研究是一项开放标签、2:l随机、3期研究,比较Rova-T与拓扑替康作为DLL3高表达的晚期或转移性SCLC的二线治疗方案。Rova-T(0.3mg/kg)在42天周期的第1天静脉给药,共两个周期,符合方案定义的继续给药标准的患者可再接受两个周期。拓扑替康(1.5mg/m²)在21天周期的第1至5天静脉给药。主要终点是总生存期(OS)。

结果

随机接受Rova-T(n = 296)和拓扑替康(n = 148)治疗的患者纳入疗效分析。中位年龄为64岁,77%的患者在初始诊断时患有广泛期疾病。Rova-T组的中位OS(95%置信区间)为6.3个月(5.6 - 7.3),拓扑替康组为8.6个月(7.7 - 10.1)(风险比,1.46 [95%置信区间:1.17 - 1.82])。一个独立的数据监测委员会建议停止入组,因为与拓扑替康相比,Rova-T组观察到的OS更短。两种药物的安全性概况与既往报告一致。

结论

与目前作为标准二线化疗药物的拓扑替康相比,Rova-T在SCLC患者中显示出较差的OS,以及更高的浆膜腔积液、光敏反应和外周水肿发生率。该人群中仍存在大量未满足的治疗需求。

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