Yagishita Shigehiro, Goto Yasushi, Nishio Makoto, Akamatsu Hiroaki, Hayashi Hidetoshi, Miura Satoru, Tamada Koji, Kagamu Hiroshi, Hamada Akinobu, Ohuchi Mayu, Gemma Akihiko, Yoshino Ichiro, Misumi Toshihiro, Hata Akito, Hara Satoshi, Kijima Takashi, Masaki Fujita, Iwasawa Shunichiro, Nakagawa Shintaro, Tatsuno Masahiro, Mitsudomi Tetsuya
Division of Molecular Pharmacology, National Cancer Center Research Institute, Tokyo, Japan.
Department of Thoracic Oncology, National Cancer Center Hospital, Tokyo, Japan.
JTO Clin Res Rep. 2024 May 16;5(7):100683. doi: 10.1016/j.jtocrr.2024.100683. eCollection 2024 Jul.
This study validated real-world pharmacokinetic (PK) data using an established population PK (PopPK) model for atezolizumab in Japanese patients with NSCLC and explored the relationship between PK parameters, effectiveness, and adverse events (AEs) for the 1200 mg once every three weeks regimen.
A subgroup of 262 of 1039 patients from J-TAIL consented to this exploratory research for PK evaluation of atezolizumab monotherapy for unresectable advanced/recurrent NSCLC (August 2018 to October 2019; 197 institutions). We evaluated plasma concentrations before the start of the third cycle of atezolizumab infusion classified into quartiles 1 to 4, their association with effectiveness, and the association between atezolizumab maximum plasma concentrations (C) calculated using the existing PopPK model and AEs of special interest (AESIs).
Overall, 175 of 262 patients were included; baseline characteristics were similar to those of patients enrolled in J-TAIL (Eastern Cooperative Oncology Group performance status ≥ 2, 12.0%; age ≥ 75 y, 28.9%; atezolizumab as more than or equal to third-line treatment, 57.5%). Atezolizumab plasma concentrations were similar to previously reported data among Japanese/non-Japanese patients. The overall survival was significantly shorter in patients with lower atezolizumab plasma concentrations in Q1 versus Q2 to Q4, although progression-free survival remained the same. The PK data adequately fit the PopPK model, with the frequency of AESIs increasing as the calculated C at cycle 1 increased.
In real-world Japanese patients with unresectable advanced/recurrent NSCLC, PKs were similar to previous reports. Certain patient populations had shorter overall survival, and atezolizumab plasma concentrations in cycle 3 were lower in this population. Elevated C at cycle 1 may be associated with an increased frequency of AESIs.
本研究使用已建立的阿替利珠单抗群体药代动力学(PopPK)模型,对日本非小细胞肺癌(NSCLC)患者的真实世界药代动力学(PK)数据进行了验证,并探讨了每三周一次1200mg给药方案的PK参数、有效性和不良事件(AE)之间的关系。
来自J-TAIL研究的1039例患者中的262例患者组成的亚组同意参与这项探索性研究,以评估阿替利珠单抗单药治疗不可切除的晚期/复发性NSCLC的PK(2018年8月至2019年10月;197家机构)。我们评估了阿替利珠单抗输注第三个周期开始前分为四分位数1至4的血浆浓度、它们与有效性的关联,以及使用现有PopPK模型计算的阿替利珠单抗最大血浆浓度(Cmax)与特别关注的AE(AESI)之间的关联。
总体而言,纳入了262例患者中的175例;基线特征与J-TAIL研究中入组患者相似(东部肿瘤协作组体能状态≥2,12.0%;年龄≥75岁,28.9%;阿替利珠单抗作为三线及以上治疗,57.5%)。阿替利珠单抗血浆浓度与日本/非日本患者先前报告的数据相似。与四分位数2至4相比,四分位数1中阿替利珠单抗血浆浓度较低的患者总生存期显著缩短,尽管无进展生存期保持不变。PK数据充分符合PopPK模型,随着第1周期计算的Cmax增加,AESI的发生率增加。
在真实世界的日本不可切除的晚期/复发性NSCLC患者中,PK与先前报告相似。某些患者群体总生存期较短,且该群体第3周期的阿替利珠单抗血浆浓度较低。第1周期Cmax升高可能与AESI发生率增加有关。