Department of Experimental Therapeutics, National Cancer Center Hospital, Tsukiji 5-1-1, Chuo-Ku, Tokyo, 104-0045, Japan.
Chugai Pharmaceutical Co., Ltd, 1-1 Nihonbashi-Muromachi 2-Chome Chuo-Ku, Tokyo, 103-8324, Japan.
Cancer Chemother Pharmacol. 2024 Jul;94(1):109-115. doi: 10.1007/s00280-023-04627-3. Epub 2024 Jan 11.
Tiragolumab is a monoclonal antibody that binds to the inhibitory immune checkpoint TIGIT (T-cell immunoreceptor with Ig and ITIM domains). In early phase clinical trials, tiragolumab in combination with the programmed death-ligand 1-inhibitor atezolizumab was well tolerated and has demonstrated preliminary anti-tumor activity in patients with advanced/metastatic solid tumors. We report the results of a phase I study of tiragolumab plus atezolizumab in Japanese patients (jRCT2080224926).
Japanese patients ≥ 20 years old received tiragolumab (600 mg) and atezolizumab (1200 mg) intravenously every 21 days until unacceptable toxicity or disease progression. Primary endpoints were safety and pharmacokinetic (PK) parameters of tiragolumab plus atezolizumab. Secondary endpoints were anti-tumor activity.
Three patients were enrolled with diagnoses of non-small cell lung cancer, pancreatic cancer, and cholangiocarcinoma. No dose-limiting toxicities were observed. Two patients experienced treatment-related adverse events (AEs) of any grade. There were no grade ≥ 3 AEs, serious AEs, AEs leading to discontinuation, modification or withdrawal of any study drug, or AEs leading to death. At cycle 1, mean PK parameters of tiragolumab were as follows: C 217 μg/mL; C 54.9 μg/mL; area under the concentration-time curve from 0 to the last measurable concentration, 2000 μg·day/mL; t, 17.6 days. Best overall response was stable disease in two patients.
Tiragolumab plus atezolizumab was well tolerated in Japanese patients with advanced/metastatic solid tumors, and no differences in tiragolumab PK characteristics were noted between Japanese patients enrolled in this study, and non-Japanese patients enrolled in a global phase Ia/Ib study. These results may support the inclusion of Japanese patients in ongoing global phase III clinical trials.
jRCT2080224926.
替利珠单抗是一种单克隆抗体,可与抑制性免疫检查点 TIGIT(T 细胞免疫受体与 Ig 和 ITIM 结构域)结合。在早期临床试验中,替利珠单抗与程序性死亡配体 1 抑制剂阿替利珠单抗联合使用具有良好的耐受性,并在晚期/转移性实体瘤患者中显示出初步的抗肿瘤活性。我们报告了一项替利珠单抗联合阿替利珠单抗在日本患者中的 I 期研究结果(jRCT2080224926)。
年龄≥20 岁的日本患者接受替利珠单抗(600mg)和阿替利珠单抗(1200mg)静脉输注,每 21 天一次,直到出现无法耐受的毒性或疾病进展。主要终点是替利珠单抗联合阿替利珠单抗的安全性和药代动力学(PK)参数。次要终点是抗肿瘤活性。
3 名患者被诊断为非小细胞肺癌、胰腺癌和胆管癌。未观察到剂量限制毒性。2 名患者发生任何级别与治疗相关的不良事件(AE)。无 3 级及以上 AE、严重 AE、导致任何研究药物修改或停药或导致死亡的 AE。在第 1 周期时,替利珠单抗的平均 PK 参数如下:C 217μg/mL;C 54.9μg/mL;0 至最后可测量浓度的浓度-时间曲线下面积,2000μg·day/mL;t 17.6 天。2 名患者的最佳总体反应为疾病稳定。
替利珠单抗联合阿替利珠单抗在晚期/转移性实体瘤的日本患者中具有良好的耐受性,且本研究入组的日本患者与全球 I 期/Ib 期研究入组的非日本患者之间,替利珠单抗 PK 特征无差异。这些结果可能支持将日本患者纳入正在进行的全球 III 期临床试验。
jRCT2080224926。