Second-line treatment of PD-1 and CTLA-4 blockade combined with liposomal irinotecan plus leucovorin and fluorouracil for advanced cholangiocarcinoma: study protocol of a single-arm, prospective phase II trial.

IF 4.3 2区 医学 Q2 ONCOLOGY
Therapeutic Advances in Medical Oncology Pub Date : 2024-10-28 eCollection Date: 2024-01-01 DOI:10.1177/17588359241292264
Heqi Yang, Linjuan Li, Xiaofen Li, Yuhang Ma, Yu Yang, Dan Cao
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引用次数: 0

Abstract

Background: Cholangiocarcinoma is a kind of malignant tumor that originates in the epithelium of the biliary tract. Although there are several options for second-line treatment for patients without specific genetic mutations, the overall treatment efficacy is disappointing. Second-line treatment which is composed of liposomal irinotecan plus fluorouracil and leucovorin significantly improved the treatment efficacy for advanced biliary tract cancer and extended patient survival. This study aims to evaluate the efficacy and safety of the combination of cadonilimab with liposomal irinotecan plus fluorouracil and leucovorin for advanced biliary tract cancer.

Objectives: The primary objective of this study is to determine the objective response rate. The second objectives of this study are overall survival, progression-free survival, disease control rate, and adverse event incidence rate.

Design: The study is a single-arm, prospective phase II clinical trial. In all, 51 patients who are diagnosed with locally advanced or metastatic bile tract cancer will be enrolled.

Methods and analysis: Eligible participants will receive cadonilimab at a dosage of 6 mg/kg on day 1 of each 21-day cycle combined with intravenous liposomal irinotecan at a dosage of 70 mg/m2 for 90 min on day 1 plus leucovorin at a dosage of 400 mg/m2 for 30 min on day 1 and fluorouracil at a dosage of 400 mg/m2 for 46 h every 2 weeks.

Discussion: Previous studies have suggested that there is a synergistic effect between the two treatment modalities. However, the potential of cadonilimab in bile tract cancer has not been explored. Hence, this trial is the first to investigate its efficacy and toxicity. In addition, the trial is also willing to explore potential biomarkers in patients with locally advanced and metastatic bile tract cancer.

Trial registration: This study was registered on ClinicalTrials.gov with NCT06438822.

Ethics: This study protocol and amendments have been approved by the Ethics Committee of West China Hospital (2024(791)).

PD-1和CTLA-4阻滞剂联合脂质体伊立替康加白血病素和氟尿嘧啶治疗晚期胆管癌的二线治疗:单臂前瞻性II期试验研究方案。
背景:胆管癌是一种起源于胆道上皮的恶性肿瘤:胆管癌是一种起源于胆道上皮的恶性肿瘤。虽然对于没有特定基因突变的患者,有多种二线治疗方案可供选择,但总体疗效令人失望。由脂质体伊立替康+氟尿嘧啶和亮菌甲素组成的二线治疗可显著提高晚期胆道癌的疗效,并延长患者的生存期。本研究旨在评估卡多尼单抗与脂质体伊立替康加氟尿嘧啶和白血病素联合治疗晚期胆道癌的疗效和安全性:本研究的首要目标是确定客观反应率。研究的第二个目标是总生存期、无进展生存期、疾病控制率和不良反应发生率:本研究是一项单臂、前瞻性 II 期临床试验。方法和分析:符合条件的参与者将在每个 21 天周期的第 1 天接受剂量为 6 毫克/千克的卡多尼单抗治疗,同时在第 1 天静脉注射剂量为 70 毫克/平方米、持续 90 分钟的脂质体伊立替康,再加上第 1 天剂量为 400 毫克/平方米、持续 30 分钟的亮菌甲素,以及每 2 周剂量为 400 毫克/平方米、持续 46 小时的氟尿嘧啶:讨论:以往的研究表明,两种治疗方式之间存在协同效应。然而,卡多尼单抗在胆道癌中的应用潜力尚未被发掘。因此,本试验是首次研究其疗效和毒性。此外,该试验还愿意探索局部晚期和转移性胆道癌患者的潜在生物标志物:本研究已在ClinicalTrials.gov上注册,注册号为NCT06438822.伦理:本研究方案及修正案已经华西医院伦理委员会批准(2024(791))。
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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来源期刊
CiteScore
8.20
自引率
2.00%
发文量
160
审稿时长
15 weeks
期刊介绍: Therapeutic Advances in Medical Oncology is an open access, peer-reviewed journal delivering the highest quality articles, reviews, and scholarly comment on pioneering efforts and innovative studies in the medical treatment of cancer. The journal has a strong clinical and pharmacological focus and is aimed at clinicians and researchers in medical oncology, providing a forum in print and online for publishing the highest quality articles in this area. This journal is a member of the Committee on Publication Ethics (COPE).
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