Sustained Clinical Benefit and Intracranial Activity of Tarlatamab in Previously Treated Small Cell Lung Cancer: DeLLphi-300 Trial Update.

IF 42.1 1区 医学 Q1 ONCOLOGY
Afshin Dowlati, Horst-Dieter Hummel, Stephane Champiat, Maria Eugenia Olmedo, Michael Boyer, Kai He, Neeltje Steeghs, Hiroki Izumi, Melissa L Johnson, Tatsuya Yoshida, Hasna Bouchaab, Hossein Borghaei, Enriqueta Felip, Philipp J Jost, Shirish Gadgeel, Xi Chen, Youfei Yu, Pablo Martinez, Amanda Parkes, Luis Paz-Ares
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引用次数: 0

Abstract

Clinical trials frequently include multiple end points that mature at different times. The initial report, typically based on the primary end point, may be published when key planned co-primary or secondary analyses are not yet available. Clinical Trial Updates provide an opportunity to disseminate additional results from studies, published in JCO or elsewhere, for which the primary end point has already been reported.Tarlatamab, a bispecific T-cell engager immunotherapy targeting delta-like ligand 3, has shown durable anticancer activity and manageable safety in previously treated small cell lung cancer (SCLC) in DeLLphi-300 phase I and DeLLphi-301 phase II trials. Here, we report extended follow-up of DeLLphi-300 (median follow-up, 12.1 months [range, 0.2-34.3]) in fully enrolled cohorts treated with tarlatamab ≥10 mg dose administered once every two weeks, once every three weeks, or once on day 1 and once on day 8 of a 21-day cycle (N = 152). Overall, the objective response rate (ORR) was 25.0%; the median duration of response (mDOR) was 11.2 months (95% CI, 6.6 to 22.3), and the median overall survival (mOS) was 17.5 months (95% CI, 11.4 to not estimable [NE]). Among 17 patients receiving 10 mg tarlatamab once every two weeks, the ORR was 35.3%, the mDOR was 14.9 months (95% CI, 3.0 to NE), the mOS was 20.3 months (95% CI, 5.1 to NE), and 29.4% had sustained disease control with time on treatment ≥52 weeks. No new safety signals were identified. In modified Response Assessment in Neuro-Oncology Brain Metastases analyses, CNS tumor shrinkage of ≥30% was observed in 62.5% of patients (10 of 16) who had a baseline CNS lesion of ≥10 mm, including in a subset of patients with tumor shrinkage long after previous brain radiotherapy. In DeLLphi-300 extended follow-up, tarlatamab demonstrated unprecedented survival and potential findings of intracranial activity in previously treated SCLC.

塔拉他单抗对曾接受过治疗的小细胞肺癌的持续临床获益和颅内活性:DeLLphi-300试验更新。
临床试验经常包括多个终点,这些终点在不同时间成熟。最初的报告通常以主要终点为基础,可能会在关键的计划共同主要分析或次级分析尚未完成时发表。Tarlatamab是一种靶向δ样配体3的双特异性T细胞吸引免疫疗法,在DeLLphi-300Ⅰ期和DeLLphi-301Ⅱ期试验中,Tarlatamab在既往治疗过的小细胞肺癌(SCLC)中显示出持久的抗癌活性和可控的安全性。在此,我们报告了DeLLphi-300的延长随访(中位随访时间为12.1个月[0.2-34.3个月]),在完全入组的队列中,塔拉他单抗剂量≥10毫克,每两周给药一次,每三周给药一次,或在21天周期的第1天和第8天各给药一次(N = 152)。总体而言,客观反应率(ORR)为25.0%;中位反应持续时间(mDOR)为11.2个月(95% CI,6.6-22.3),中位总生存期(mOS)为17.5个月(95% CI,11.4-无法估计[NE])。在每两周接受一次10毫克塔拉他单抗治疗的17名患者中,ORR为35.3%,mDOR为14.9个月(95% CI,3.0至NE),mOS为20.3个月(95% CI,5.1至NE),29.4%的患者在治疗时间≥52周时疾病得到持续控制。未发现新的安全性信号。在修改后的《神经肿瘤脑转移反应评估》分析中,基线中枢神经系统病灶≥10毫米的患者中有62.5%(16人中有10人)观察到中枢神经系统肿瘤缩小≥30%,其中包括既往接受过脑放疗后肿瘤长期缩小的患者。在DeLLphi-300的延长随访中,塔拉他单抗在既往接受过治疗的SCLC患者中显示出前所未有的生存率和颅内活动的潜在发现。
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 Clinical Oncology
Journal of Clinical Oncology 医学-肿瘤学
CiteScore
41.20
自引率
2.20%
发文量
8215
审稿时长
2 months
期刊介绍: The Journal of Clinical Oncology serves its readers as the single most credible, authoritative resource for disseminating significant clinical oncology research. In print and in electronic format, JCO strives to publish the highest quality articles dedicated to clinical research. Original Reports remain the focus of JCO, but this scientific communication is enhanced by appropriately selected Editorials, Commentaries, Reviews, and other work that relate to the care of patients with cancer.
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