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Sintilimab plus nab-paclitaxel as second-line treatment for advanced biliary tract cancer: study protocol for an investigator-initiated phase 2 trial (NapaSinti trial). | LitMetric

AI Article Synopsis

  • Biliary tract cancer (BTC) is a rare and aggressive type of cancer with limited treatment options, particularly for patients lacking specific genetic mutations; the study explores combining sintilimab (an immunotherapy) with nab-paclitaxel (a chemotherapy) to improve outcomes.
  • The NapaSinti trial is a phase 2, nonrandomized study in China focusing on patients aged 18-75 with advanced BTC who have progressed after previous chemotherapy; they will receive a combination of sintilimab and nab-paclitaxel every three weeks.
  • The main goal of the trial is to measure the objective response rate (ORR), while secondary aims include overall survival, progression-free survival, safety, and identifying potential biomarkers

Article Abstract

Background: Biliary tract cancer (BTC) is a relatively rare but highly aggressive malignancy. However, there is currently no satisfactory second-line regimen for patients without specific genetic mutations. Nanoparticle albumin-bound paclitaxel, also known as nab-paclitaxel (Abraxane, Bristol Myers Squibb), has shown activity in patients with BTC. Studies investigating the immunogenic features of BTC suggested that checkpoint inhibition may lead to antitumor immune responses. In recent years, improved survival has been observed in patients treated with chemotherapy combined with immunotherapy across multiple cancer types, including BTC. This clinical trial aims to evaluate the efficacy and safety of second-line sintilimab in combination with nab-paclitaxel in advanced BTC patients.

Methods: The NapaSinti trial is a prospective, nonrandomized, open-label, phase 2 study conducted at a tertiary hospital in Chengdu, China. Eligible patients are those with histologically or cytologically confirmed locally advanced non-resectable or metastatic adenocarcinoma in the biliary tract (including intrahepatic cholangiocarcinoma, extrahepatic cholangiocarcinoma, and gallbladder cancer), aged between 18 and 75 years, with an Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1, who have experienced disease progression after prior gemcitabine- or fluorouracil-based chemotherapy and have not received taxane or immune checkpoint inhibitor treatment. Enrolled patients will receive intravenous administration of sintilimab 200 mg on day 1 and nab-paclitaxel 125 mg/m2 on days 1 and 8, every three weeks. The primary endpoint is the objective response rate (ORR), while the secondary endpoints include overall survival (OS), progression-free survival (PFS), and safety. Exploratory objectives aim to identify biomarkers and molecular signatures for predicting response or prognosis. Using Simon's two-stage design, a total of 63 participants will be enrolled in the study. This trial was initiated in March 2022 in China.

Discussion: The NapaSinti trial evaluates the efficacy and safety of second-line sintilimab plus nab-paclitaxel for advanced biliary tract cancer. Additionally, the trial provides an opportunity for translational research.

Trial Registration: Chinese Clinical Trial Registry ChiCTR2100052118. Registered October 19, 2021.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10405505PMC
http://dx.doi.org/10.1186/s12885-023-11188-4DOI Listing

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