Department of Oncology Center, Yamaguchi University Hospital, Yamaguchi, Japan.
Department of Cancer Survey and Gastrointestinal Oncology, Osaka International Cancer Institute, Osaka, Japan.
J Hepatobiliary Pancreat Sci. 2023 Jan;30(1):102-110. doi: 10.1002/jhbp.1219. Epub 2022 Aug 9.
Gemcitabine/cisplatin (GC) combination therapy has been the standard palliative chemotherapy for patients with advanced biliary tract cancer (BTC). No randomized clinical trials have been able to demonstrate the survival benefit over GC during the past decade. In our previous phase II trial, adding S-1 to GC (GCS) showed promising efficacy and we aimed to determine whether GCS could improve overall survival compared with GC for patients with advanced BTC.
We performed a mulitcenter, randomized phase III trial across 39 centers. Enrolled patients were randomly allocated (1:1) to either the GCS or GC arm. The GCS regimen comprised gemcitabine (1000 mg/m ) and cisplatin (25 mg/m ) infusion on day 1 and 80 mg/m of S-1 on days 1-7 every 2 weeks. The primary endpoint was overall survival (OS) and the secondary endpoints were progression-free survival (PFS), response rate (RR), and adverse events (AEs). This study is registered with Clinical trial identification: NCT02182778.
Between July 2014 and February 2016, 246 patients were enrolled. The median OS and 1-year OS rate were 13.5 months and 59.4% in the GCS arm and 12.6 months and 53.7% in the GC arm, respectively (hazard ratio [HR] 0.79, 90% confidence interval [CI]: 0.628-0.996; P = .046 [stratified log-rank test]). Median PFS was 7.4 months in the GCS arm and 5.5 months in the GC arm (HR 0.75, 95% CI: 0.577-0.970; P = .015). RR was 41.5% in the GCS arm and 15.0% in the GC arm. Grade 3 or worse AEs did not show significant differences between the two arms.
GCS is the first regimen which demonstrated survival benefits as well as higher RR over GC in a randomized phase III trial and could be the new first-line standard chemotherapy for advanced BTC. To exploit the advantage of its high RR, GCS is now tested in the neoadjuvant setting in a randomized phase III trial for potentially resectable BTC.
吉西他滨/顺铂(GC)联合化疗一直是晚期胆道癌(BTC)患者的标准姑息性化疗。在过去十年中,没有随机临床试验能够证明 GC 治疗的生存获益优于 GC。在我们之前的 II 期试验中,吉西他滨/顺铂(GCS)联合 S-1 显示出有希望的疗效,我们旨在确定 GCS 是否可以改善晚期 BTC 患者的总生存期。
我们在 39 个中心进行了一项多中心、随机 III 期试验。入组患者被随机分配(1:1)至 GCS 或 GC 组。GCS 方案包括吉西他滨(1000mg/m )和顺铂(25mg/m )输注第 1 天和第 80mg/m 的 S-1 第 1-7 天,每 2 周一次。主要终点是总生存期(OS),次要终点是无进展生存期(PFS)、反应率(RR)和不良事件(AE)。这项研究在 ClinicalTrials.gov 注册,注册号为 NCT02182778。
2014 年 7 月至 2016 年 2 月期间,共纳入 246 例患者。GCS 组中位 OS 和 1 年 OS 率分别为 13.5 个月和 59.4%,GC 组分别为 12.6 个月和 53.7%(风险比 [HR]0.79,90%置信区间 [CI]:0.628-0.996;P=0.046[分层对数秩检验])。GCS 组中位 PFS 为 7.4 个月,GC 组为 5.5 个月(HR0.75,95%CI:0.577-0.970;P=0.015)。GCS 组 RR 为 41.5%,GC 组为 15.0%。两组 3 级或更高级别的 AE 无显著差异。
GCS 是第一项在随机 III 期试验中显示出生存获益和更高 RR 的方案,可能成为晚期 BTC 的新一线标准化疗。为了发挥其高 RR 的优势,GCS 现在正在一项潜在可切除 BTC 的随机 III 期试验中进行新辅助治疗。