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