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厄洛替尼联合吉西他滨和奥沙利铂作为可切除的胆管癌患者的辅助治疗:基于 ctDNA 的、多中心、开放标签、随机、对照、II 期临床试验研究方案。

Afatinib in combination with GEMOX chemotherapy as the adjuvant treatment in patients with ErbB pathway mutated, resectable gallbladder cancer: study protocol for a ctDNA-based, multicentre, open-label, randomised, controlled, phase II trial.

机构信息

Department of Biliary-Pancreatic Surgery, Shanghai Jiao Tong University School of Medicine Affiliated Renji Hospital, Shanghai, Shanghai, China.

State Key Laboratory of Oncogenes and Related Genes, Shanghai Cancer Institute, Shanghai, Shanghai, China.

出版信息

BMJ Open. 2023 Feb 28;13(2):e061892. doi: 10.1136/bmjopen-2022-061892.

Abstract

INTRODUCTION

Gallbladder cancer (GBC) is an aggressive type of digestive system cancer with a dismal outcome. Given the lack of effective treatment options, the disease rapidly reoccurs and 5-year survival rate is <5%. Our team previously found that a significant percentage of GBC tissues harboured mutations of the ErbB-related pathway. Afatinib is a chemically synthesised drug specifically targeting the ErbB pathway mutations. However, its efficacy in the treatment of patients with GBC remains unknown. Circulating tumour DNA (ctDNA) refers to a proportion of cell-free DNA in the blood which is released by apoptotic and necrotic cells from tumours in situ, metastatic foci or circulating tumour cells. ctDNA-based liquid biopsy is a non-invasive pathological detection method that offers additional value to evaluate the therapeutic efficacy of antitumour drugs.

METHODS AND ANALYSIS

We conduct a multicentre and randomised study on afatinib combined with gemcitabine and oxaliplatin (GEMOX) in patients with ErbB pathway mutated GBC. Clinical and biological evaluation involving ErbB pathway ctDNA detection will be made during the 3-year follow-up after participation. The primary objective of this clinical trial is to evaluate the clinical efficacy of afatinib. Disease-free survival is the primary end point and will be correlated with plasma ctDNA of patients in the treatment with afatinib. In addition, we will evaluate the sensitivity and specificity of plasma ctDNA for monitoring tumour recurrence and progression. Finally, we will assess the safety of afatinib by keeping an eye on the safety indicators.

ETHICS AND DISSEMINATION

The study was approved by the medical-ethical review committee of Xinhua Hospital Affiliated to Shanghai Jiao Tong University School of Medicine and Renji Hospital Affiliated to Shanghai Jiao Tong University School of Medicine. The clinical trials results, even inconclusive, will be published in peer-reviewed journals.

TRIAL REGISTRATION NUMBER

NCT04183712.

摘要

简介

胆囊癌(GBC)是一种侵袭性消化系统癌症,预后较差。由于缺乏有效的治疗选择,该疾病迅速复发,5 年生存率<5%。我们的团队之前发现,相当一部分 GBC 组织存在 ErbB 相关通路的突变。阿法替尼是一种专门针对 ErbB 通路突变的化学合成药物。然而,其在 GBC 患者治疗中的疗效尚不清楚。循环肿瘤 DNA(ctDNA)是指血液中无细胞游离 DNA 的一部分,它是原位肿瘤、转移灶或循环肿瘤细胞中的凋亡和坏死细胞释放的。ctDNA 为基础的液体活检是一种非侵入性的病理检测方法,为评估抗肿瘤药物的治疗效果提供了额外的价值。

方法和分析

我们在 ErbB 通路突变的 GBC 患者中进行了一项阿法替尼联合吉西他滨和奥沙利铂(GEMOX)的多中心、随机研究。在参与后的 3 年随访期间,将进行包括 ErbB 通路 ctDNA 检测在内的临床和生物学评估。这项临床试验的主要目的是评估阿法替尼的临床疗效。无病生存期是主要终点,并将与接受阿法替尼治疗的患者的血浆 ctDNA 相关联。此外,我们将评估血浆 ctDNA 监测肿瘤复发和进展的敏感性和特异性。最后,我们将通过关注安全指标来评估阿法替尼的安全性。

伦理和传播

该研究得到了上海交通大学医学院附属新华医院和上海交通大学医学院附属仁济医院医学伦理审查委员会的批准。即使结果不确定,临床试验结果也将在同行评议期刊上发表。

注册号

NCT04183712。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f42c/9980349/5725227f8127/bmjopen-2022-061892f01.jpg

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