Temporal dynamics of CLDN18.2 expression following zolbetuximab treatment in advanced gastric cancer

K. Yamamoto , I. Nakayama , N. Sakamoto , Y. Matsubara , Y. Miyashita , A. Kobayashi , U. Okazaki , D. Okemoto , K. Seguchi , T. Hosokai , T. Ogura , S. Mishima , D. Kotani , A. Kawazoe , T. Hashimoto , Y. Kuboki , H. Bando , T. Kojima , T. Yoshino , T. Kuwata , K. Shitara
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Abstract

Background

Zolbetuximab plus chemotherapy is the standard of care for unresectable advanced gastric cancer that is human epidermal growth factor receptor 2-negative and claudin-18 isoform 2 (CLDN18.2)-positive (2+/3+ staining intensity in ≥75% of tumor cells). The dynamics of CLDN18.2 expression after zolbetuximab remain poorly understood.

Materials and methods

Using immunohistochemistry, we retrospectively assessed CLDN18.2 expression in tumor samples from CLDN18.2-positive advanced gastric cancer collected before and after zolbetuximab-containing chemotherapy. Expression levels were evaluated based on the proportion of cells with ≥2+ staining intensity using multiple cut-off values (75%, 40%, and 25%).

Results

Among 65 patients who received zolbetuximab-containing therapy, CLDN18.2 status was assessable at both baseline and disease progression in 15 patients. At disease progression, 53.3% of cases converted to CLDN18.2-negative. CLDN18.2 positivity was retained in 66.7% and 73.3% of patients when applying 40% and 25% cut-off levels, respectively.

Conclusions

CLDN18.2 expression above the ≥75% cut-off declined after zolbetuximab, but lower-level expression was often preserved, supporting the potential for subsequent targeted therapy.
唑仑妥昔单抗治疗晚期胃癌后CLDN18.2表达的时间动态
背景唑贝昔单抗联合化疗是不可切除的晚期胃癌的标准治疗方案,患者为人表皮生长因子受体2阴性和CLDN18.2阳性(2+/3+染色强度≥75%的肿瘤细胞)。唑贝昔单抗后CLDN18.2表达的动态尚不清楚。材料与方法采用免疫组化方法,回顾性分析了晚期胃癌患者CLDN18.2阳性肿瘤样本在唑苯妥昔单抗化疗前后的表达情况。根据≥2+染色强度的细胞比例,使用多个截止值(75%、40%和25%)评估表达水平。结果在65例接受含唑苯妥昔单抗治疗的患者中,15例患者的CLDN18.2状态在基线和疾病进展时均可评估。在疾病进展时,53.3%的病例转化为cldn18.2阴性。当应用40%和25%临界值时,CLDN18.2阳性分别在66.7%和73.3%的患者中保留。结论在≥75%临界值后,唑贝昔单抗治疗后,CLDN18.2的表达水平下降,但通常保留较低水平的表达,支持后续靶向治疗的可能性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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