Plain language summary: tarlatamab for patients with previously treated small cell lung cancer.

IF 3 4区 医学 Q2 ONCOLOGY Future oncology Pub Date : 2024-11-12 DOI:10.1080/14796694.2024.2402152
Myung-Ju Ahn, Byoung Chul Cho, Enriqueta Felip, Ippokratis Korantzis, Kadoaki Ohashi, Margarita Majem, Oscar Juan-Vidal, Sabin Handzhiev, Hiroki Izumi, Jong-Seok Lee, Rafal Dziadziuszko, Jürgen Wolf, Fiona Blackhall, Martin Reck, Jean Bustamante Alvarez, Horst-Dieter Hummel, Anne-Marie C Dingemans, Jacob Sands, Hiroaki Akamatsu, Taofeek K Owonikoko, Suresh S Ramalingam, Hossein Borghaei, Melissa L Johnson, Shuang Huang, Sujoy Mukherjee, Mukul Minocha, Tony Jiang, Pablo Martinez, Erik S Anderson, Luis Paz-Ares
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Abstract

What is this summary about?: This is a summary of a phase 2 clinical study called DeLLphi-301. The study looked at how effective and safe a medicine called tarlatamab was in participants with small cell lung cancer (SCLC). Participants previously received at least two other treatments for their SCLC. Tarlatamab is a new medicine that locates a protein called DLL3 on the cancer, which allows T cells to attack the cancer. T cells belong to the body's natural defense system known as the immune system. The DeLLphi-301 study separated participants into two groups to receive tarlatamab 10 mg or 100 mg to determine which dose best shrank SCLC with minimal side effects. All participants received a small first dose (1 mg tarlatamab) to decrease the risk of an immune system reaction called cytokine release syndrome (CRS). Tarlatamab was given through the participant's vein once every 2 weeks. This method of administration is known as intravenous (IV) infusion.

What were the results of the dellphi-301 study?: In the group given 10 mg tarlatamab, 40% of participants responded to treatment (cancer shrank). In the group given 100 mg tarlatamab, 32% of participants responded to treatment (cancer shrank). After taking tarlatamab at either dose, 59% of participants lived for at least 6 months without their cancer growing or getting worse.The most common side effect was CRS, which occurred in 51% of participants in the group given 10 mg tarlatamab and 61% of participants in the group given 100 mg tarlatamab. Other common side effects were decreased appetite, fever, constipation, and anemia. Some participants had a type of immune reaction called immune effector cell-associated neurotoxicity syndrome (ICANS). A small number of participants (3%) stopped taking tarlatamab because of side effects related to tarlatamab.

What do the results from the dellphi-301 study mean?: The study found that tarlatamab given every 2 weeks shrank SCLC in participants with SCLC who received previous treatments. Participants given the 10 mg tarlatamab dose had fewer side effects than those given the 100 mg tarlatamab dose.Clinical Trial Registration: NCT05740566 (DeLLphi-304) (ClinicalTrials.gov).

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通俗易懂的摘要:用于既往接受过治疗的小细胞肺癌患者的替拉他单抗。
本摘要是关于什么的? 这是一项名为 DeLLphi-301 的 2 期临床研究的摘要。该研究考察了一种名为塔拉他单抗的药物对小细胞肺癌(SCLC)患者的有效性和安全性。参试者之前至少接受过两种其他治疗方法来治疗小细胞肺癌。塔拉他单抗是一种新药,它能将一种名为DLL3的蛋白质定位在癌症上,从而让T细胞攻击癌症。T细胞属于人体的天然防御系统,即免疫系统。DeLLphi-301研究将参与者分成两组,分别接受10毫克或100毫克的tarlatamab治疗,以确定哪种剂量能最大程度地缩小SCLC,同时将副作用降到最低。所有参与者首次接受的剂量都很小(1 毫克塔拉他单抗),以降低免疫系统反应(称为细胞因子释放综合征 (CRS))的风险。塔拉他单抗每两周通过参与者的静脉注射一次。dellphi-301研究的结果如何?在服用10毫克塔拉他单抗的小组中,40%的参与者对治疗有反应(癌症缩小)。在服用100毫克塔拉他单抗的小组中,32%的参与者对治疗有反应(癌症缩小)。最常见的副作用是CRS,在服用10毫克塔拉他单抗的组别中,51%的参与者出现了CRS,在服用100毫克塔拉他单抗的组别中,61%的参与者出现了CRS。其他常见的副作用包括食欲下降、发烧、便秘和贫血。一些参与者出现了一种称为免疫效应细胞相关神经毒性综合征(ICANS)的免疫反应。dellphi-301研究的结果意味着什么? 该研究发现,每2周服用一次tarlatamab可使曾接受过治疗的SCLC患者的SCLC缩小。与服用100毫克塔拉他单抗剂量的患者相比,服用10毫克塔拉他单抗剂量的患者副作用更小:NCT05740566(DeLLphi-304)(ClinicalTrials.gov)。
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
Future oncology
Future oncology ONCOLOGY-
CiteScore
5.40
自引率
3.00%
发文量
335
审稿时长
4-8 weeks
期刊介绍: Future Oncology (ISSN 1479-6694) provides a forum for a new era of cancer care. The journal focuses on the most important advances and highlights their relevance in the clinical setting. Furthermore, Future Oncology delivers essential information in concise, at-a-glance article formats - vital in delivering information to an increasingly time-constrained community. The journal takes a forward-looking stance toward the scientific and clinical issues, together with the economic and policy issues that confront us in this new era of cancer care. The journal includes literature awareness such as the latest developments in radiotherapy and immunotherapy, concise commentary and analysis, and full review articles all of which provide key findings, translational to the clinical setting.
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