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在局部晚期不可切除或转移性胃或胃食管交界腺癌患者中,在不存在或存在zolbetuximab的情况下对氟尿嘧啶和奥沙利铂进行群体药代动力学分析。

Population pharmacokinetic analysis of fluorouracil and oxaliplatin in the absence or presence of zolbetuximab in locally advanced unresectable or metastatic gastric or gastroesophageal junction adenocarcinoma.

作者信息

Yamada Akihiro, Yang Jianning, Bonate Peter L, Heo Nakyo, Poondru Srinivasu

机构信息

Astellas Pharma, Inc., Tokyo, Japan.

Astellas Pharma Global Development, Inc., Northbrook, IL, USA.

出版信息

Cancer Chemother Pharmacol. 2025 Sep 19;95(1):89. doi: 10.1007/s00280-025-04808-2.

Abstract

PURPOSE

Zolbetuximab, a monoclonal antibody targeting claudin 18.2 (CLDN18.2), is approved in combination with chemotherapy for human epidermal growth factor receptor 2 (HER2)-negative, CLDN18.2-positive, unresectable, advanced or recurrent gastric cancer (in Japan) and in combination with fluoropyrimidine- and platinum-containing chemotherapy for first-line locally advanced unresectable or metastatic HER2-negative, CLDN18.2-positive gastric or gastroesophageal junction (G/GEJ) adenocarcinoma (in geographies including but not limited to the US, Europe, and China). Noncompartmental analysis (NCA) was previously used to evaluate the effect of zolbetuximab on pharmacokinetics (PK) of 5-fluorouracil (5-FU) and oxaliplatin; however, limitations of NCA confounded the results. This study utilized population pharmacokinetic (PopPK) analysis to address these limitations.

METHODS

In Cohort 2 of the phase 2 ILUSTRO study (NCT03505320), patients with locally advanced unresectable or metastatic HER2-negative, CLDN18.2-positive G/GEJ adenocarcinoma received zolbetuximab with modified folinic acid, 5-FU, and oxaliplatin. PopPK models were developed to evaluate the impact of zolbetuximab on PK of 5-FU and oxaliplatin (including simultaneous analysis of free and total platinum).

RESULTS

PK of 5-FU was adequately described by a 1-compartment model with zero-order input and first-order elimination. PK of free and total platinum was simultaneously described by a 3-compartment model with zero-order input, first-order elimination, and time-dependent free fraction. No impact of zolbetuximab on 5-FU PK or on systemic clearance or free fraction of oxaliplatin in plasma was observed. The effect of zolbetuximab on oxaliplatin distribution volume (12.3% decrease) was statistically significant but not considered clinically relevant.

CONCLUSION

PopPK analysis suggests no effect of zolbetuximab on 5-FU or oxaliplatin PK.

摘要

目的

zolbetuximab是一种靶向紧密连接蛋白18.2(CLDN18.2)的单克隆抗体,已被批准与化疗联合用于治疗人表皮生长因子受体2(HER2)阴性、CLDN18.2阳性、不可切除的晚期或复发性胃癌(在日本),以及与含氟嘧啶和铂的化疗联合用于一线局部晚期不可切除或转移性HER2阴性、CLDN18.2阳性的胃癌或胃食管交界(G/GEJ)腺癌(在包括但不限于美国、欧洲和中国的地区)。先前使用非房室分析(NCA)来评估zolbetuximab对5-氟尿嘧啶(5-FU)和奥沙利铂药代动力学(PK)的影响;然而,NCA的局限性使结果产生混淆。本研究利用群体药代动力学(PopPK)分析来解决这些局限性。

方法

在2期ILUSTRO研究(NCT03505320)的队列2中,局部晚期不可切除或转移性HER2阴性、CLDN18.2阳性G/GEJ腺癌患者接受了zolbetuximab联合亚叶酸钙、5-FU和奥沙利铂治疗。建立PopPK模型以评估zolbetuximab对5-FU和奥沙利铂PK的影响(包括游离铂和总铂的同步分析)。

结果

5-FU的PK通过具有零级输入和一级消除的一室模型得到充分描述。游离铂和总铂的PK通过具有零级输入、一级消除和时间依赖性游离分数的三室模型同时描述。未观察到zolbetuximab对5-FU PK或奥沙利铂的全身清除率或血浆游离分数有影响。zolbetuximab对奥沙利铂分布容积的影响(降低12.3%)具有统计学意义,但不被认为具有临床相关性。

结论

PopPK分析表明zolbetuximab对5-FU或奥沙利铂的PK没有影响。

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