术前氟尿嘧啶、亚叶酸钙、奥沙利铂和多西紫杉醇对局部晚期胃食管癌和胃癌疗效的预后指标:整合生物标志物分析和临床病理因素

IF 5.6 2区 医学 Q1 ONCOLOGY
Amane Jubashi, Izuma Nakayama, Naoya Sakamoto, Shogo Takei, Yuki Matsubara, Yu Miyashita, Seiya Sato, Shinpei Ushiyama, Akinori Kobayashi, Ukyo Okazaki, Dai Okemoto, Kazumasa Yamamoto, Saori Mishima, Daisuke Kotani, Akihito Kawazoe, Tadayoshi Hashimoto, Yoshiaki Nakamura, Yasutoshi Kuboki, Hideaki Bando, Takashi Kojima, Takayuki Yoshino, Takeshi Kuwata, Kazuma Sato, Takeo Fujita, Mitsumasa Yoshida, Masahiro Yura, Takahiro Kinoshita, Kohei Shitara
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引用次数: 0

摘要

目的:围手术期氟尿嘧啶、亚叶酸钙、奥沙利铂和多西紫杉醇(FLOT)是局部晚期胃/胃食管结癌(GC/GEJC)的标准治疗方法。生物标志物状态对围手术期FLOT疗效的影响尚不清楚。本研究评估了可切除的GC/GEJC患者的临床病理特征(包括生物标志物状态)与FLOT围手术期疗效之间的关系。患者和方法:通过回顾2020年2月至2024年3月期间接受FLOT围手术期治疗的患者的医疗记录进行回顾性观察研究。符合条件的患者有组织学证实的腺癌,cT2-4a和/或N0-3、M0期可切除的疾病,并进行了生物标志物检测。结果:在116例符合条件的患者中,人表皮生长因子受体2 (HER2)阳性的比例为7.8%,而PD-L1联合阳性评分(CPS)≥1、≥5和≥10的比例分别为90.5%、44.0%和15.5%。30.2%的患者出现cldn18亚型2 (CLDN18.2)阳性(≥75%的肿瘤细胞呈2+/3+)。主要病理缓解率(MPR)和病理完全缓解率(pCR)分别为22.4% (95% CI, 15.3 ~ 31.0)和8.6% (95% CI, 4.2 ~ 15.3)。弥散型组织学是病理反应的阴性指标。术前FLOT后CLDN18.2表达明显下降,初始CLDN18.2阳性患者H-score中位数由285.0下降至187.5 (P < 0.001)。与MPR患者相比,无MPR患者维持CLDN18.2阳性的频率更高(53.8% vs 12.5%, P = 0.05)。结论:HER2、PD-L1和CLDN18.2状态与可切除的GC/GEJC中FLOT的病理反应无关。CLDN18.2表达在术前FLOT后显著降低,但在无MPR的患者中仍然较高,提示CLDN18.2靶向治疗可能值得在围手术期进行研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Prognostic Indicators of Preoperative Fluorouracil, Leucovorin, Oxaliplatin, and Docetaxel Efficacy in Locally Advanced Gastroesophageal and Gastric Cancer: Integrating Biomarker Analysis and Clinicopathological Factors.

Prognostic Indicators of Preoperative Fluorouracil, Leucovorin, Oxaliplatin, and Docetaxel Efficacy in Locally Advanced Gastroesophageal and Gastric Cancer: Integrating Biomarker Analysis and Clinicopathological Factors.

Prognostic Indicators of Preoperative Fluorouracil, Leucovorin, Oxaliplatin, and Docetaxel Efficacy in Locally Advanced Gastroesophageal and Gastric Cancer: Integrating Biomarker Analysis and Clinicopathological Factors.

Prognostic Indicators of Preoperative Fluorouracil, Leucovorin, Oxaliplatin, and Docetaxel Efficacy in Locally Advanced Gastroesophageal and Gastric Cancer: Integrating Biomarker Analysis and Clinicopathological Factors.

Purpose: Perioperative fluorouracil, leucovorin, oxaliplatin, and docetaxel (FLOT) is a standard treatment for locally advanced gastric/gastroesophageal junction cancer (GC/GEJC). The impact of biomarker status on the efficacy of perioperative FLOT remains unclear. This study evaluated the association between clinicopathological features, including biomarker status, and the efficacy of perioperative FLOT in patients with resectable GC/GEJC.

Patients and methods: A retrospective observational study was conducted by reviewing medical records of patients treated with perioperative FLOT between February 2020 and March 2024. Eligible patients had histologically confirmed adenocarcinoma, resectable disease at stages cT2-4a and/or N0-3, M0, and underwent biomarker testing.

Results: Among 116 eligible patients, human epidermal growth factor receptor 2 (HER2) positivity was observed in 7.8%, whereas PD-L1 combined positive score (CPS) of ≥1, ≥5, and ≥10 was detected in 90.5%, 44.0%, and 15.5% of patients, respectively. Claudin-18 isoform 2 (CLDN18.2) positivity (2+/3+ in ≥75% of tumor cells) was observed in 30.2% of patients. Major pathological response (MPR) and pathological complete response (pCR) rates were 22.4% (95% CI, 15.3 to 31.0) and 8.6% (95% CI, 4.2 to 15.3), respectively. Diffuse-type histology was a negative indicator for pathological response. CLDN18.2 expression decreased significantly after preoperative FLOT, with the median H-score declining from 285.0 to 187.5 (P < .001) in patients with CLDN18.2 positivity at initiation. Maintained CLDN18.2 positivity was more frequently observed in patients without MPR compared with those with MPR (53.8% v 12.5%, P = .05).

Conclusion: HER2, PD-L1, and CLDN18.2 statuses were not linked to pathological response to FLOT in resectable GC/GEJC. CLDN18.2 expression significantly decreased after preoperative FLOT but remained higher in patients without MPR, suggesting that CLDN18.2-targeted therapy may warrant investigation in the perioperative setting.

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