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针对间皮素的 T 细胞受体融合构建细胞疗法治疗难治性实体瘤:1/2 期试验中期结果。

Mesothelin-targeting T cell receptor fusion construct cell therapy in refractory solid tumors: phase 1/2 trial interim results.

机构信息

Thoracic and GI Malignancies Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.

Princess Margaret Cancer Centre, Toronto, ON, Canada.

出版信息

Nat Med. 2023 Aug;29(8):2099-2109. doi: 10.1038/s41591-023-02452-y. Epub 2023 Jul 27.

Abstract

The T cell receptor fusion construct (TRuC) gavocabtagene autoleucel (gavo-cel) consists of single-domain anti-mesothelin antibody that integrates into the endogenous T cell receptor (TCR) and engages the signaling capacity of the entire TCR upon mesothelin binding. Here we describe phase 1 results from an ongoing phase1/2 trial of gavo-cel in patients with treatment-refractory mesothelin-expressing solid tumors. The primary objectives were to evaluate safety and determine the recommended phase 2 dose (RP2D). Secondary objectives included efficacy. Thirty-two patients received gavo-cel at increasing doses either as a single agent (n = 3) or after lymphodepletion (LD, n = 29). Dose-limiting toxicities of grade 3 pneumonitis and grade 5 bronchioalveolar hemorrhage were noted. The RP2D was determined as 1 × 10 cells per m after LD. Grade 3 or higher pneumonitis was seen in 16% of all patients and in none at the RP2D; grade 3 or higher cytokine release syndrome occurred in 25% of all patients and in 15% at the RP2D. In 30 evaluable patients, the overall response rate and disease control rate were 20% (13% confirmed) and 77%, respectively, and the 6-month overall survival rate was 70%. Gavo-cel warrants further study in patients with mesothelin-expressing cancers given its encouraging anti-tumor activity, but it may have a narrow therapeutic window. ClinicalTrials.gov identifier: NCT03907852 .

摘要

T 细胞受体融合构建体(TRuC)加维奥妥昔单抗 autoleucel(加维-cel)由单域抗间皮素抗体组成,该抗体整合到内源性 T 细胞受体(TCR)中,并在间皮素结合时利用整个 TCR 的信号转导能力。在此,我们描述了正在进行的加维-cel 治疗难治性间皮素表达实体瘤患者的 1/2 期临床试验的 1 期结果。主要目的是评估安全性并确定推荐的 2 期剂量(RP2D)。次要目标包括疗效。32 名患者以递增剂量接受加维-cel 治疗,要么作为单一药物(n=3),要么在淋巴细胞耗竭(LD,n=29)后。观察到 3 级肺炎和 5 级细支气管肺泡出血的剂量限制毒性。LD 后确定 RP2D 为 1×10 个细胞/m。所有患者中有 16%出现 3 级或更高级别的肺炎,而在 RP2D 中则没有;所有患者中有 25%出现 3 级或更高级别的细胞因子释放综合征,而在 RP2D 中则有 15%。在 30 名可评估患者中,总缓解率和疾病控制率分别为 20%(13%为确认)和 77%,6 个月总生存率为 70%。鉴于其令人鼓舞的抗肿瘤活性,加维-cel 有望在表达间皮素的癌症患者中进一步研究,但它可能具有较窄的治疗窗口。ClinicalTrials.gov 标识符:NCT03907852。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f86/10427427/c64baa58ce7f/41591_2023_2452_Fig1_HTML.jpg

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