Division of Surgical Oncology, University of Louisville School of Medicine, Louisville, KY, USA.
James Graham Brown Cancer Center Louisville, Louisville, KY, USA.
Ann Surg Oncol. 2022 Sep;29(9):5462-5473. doi: 10.1245/s10434-022-11932-3. Epub 2022 Jun 3.
Unresectable intrahepatic cholangiocarcinoma (ICC) carries a poor prognosis, and currently there are moderately established chemotherapeutic [gemcitabine/cisplatin (Gem/Cis)] treatments to prolong survival. The purpose of this study was to assess the efficacy of irinotecan drug-eluting beads (DEBIRI) therapy by transarterial infusion in combination with systemic therapy in unresectable ICC.
This is a prospective, multicenter, open-label, randomized phase II study (Clin Trials: NCT01648023-DELTIC trial) of patients with ICC randomly assigned to Gem/Cis with DEBIRI or Gem/Cis alone. The primary endpoint was response rate.
The intention-to-treat population comprised 48 patients: 24 treated with Gem/Cis and DEBIRI and 22 with Gem/Cis alone (2 screen failures). The two groups were similar with respect to the extent of liver involvement (35% versus 38%) and presence of extrahepatic disease (29% versus 14%, p = 0.12). Median numbers of chemotherapy cycles were similar (6 versus 6), as were rates of grade 3/4 adverse events (34% for the Gem/Cis-DEBIRI group versus 36% for the Gem/Cis group). The overall response rate was significantly greater in the Gem/Cis-DEBIRI arm versus the Gem/Cis arm at 2 (p < 0.04), 4 (p < 0.03), and 6 months (p < 0.05). There was significantly more downsizing to resection/ablation in the Gem/Cis-DEBIRI arm versus the Gem/Cis arm (25% versus 8%, p < 005), and there was improved median progression-free survival [31.9 (95% CI 8.5-75.3) months versus 10.1 (95% CI 5.3-13.5) months, p = 0.028] and improved overall survival [33.7 (95% CI 13.5-54.5) months versus 12.6 (95% CI 8.7-33.4) months, p = 0.048].
Combination Gem/Cis with DEBIRI is safe, and leads to significant improvement in downsizing to resection, improved progression-free survival, and overall survival.
不可切除的肝内胆管细胞癌(ICC)预后较差,目前有中度确立的化疗[吉西他滨/顺铂(Gem/Cis)]治疗方法来延长生存期。本研究的目的是评估经动脉输注伊立替康载药微球(DEBIRI)联合全身治疗不可切除 ICC 的疗效。
这是一项前瞻性、多中心、开放标签、随机 II 期研究(临床试验:NCT01648023-DELTIC 试验),纳入的 ICC 患者随机分配接受 Gem/Cis 联合 DEBIRI 或 Gem/Cis 单独治疗。主要终点是缓解率。
意向治疗人群包括 48 例患者:24 例接受 Gem/Cis 和 DEBIRI 治疗,22 例接受 Gem/Cis 单独治疗(2 例筛选失败)。两组在肝受累程度(35%比 38%)和存在肝外疾病(29%比 14%,p=0.12)方面相似。化疗周期中位数相似(6 个周期比 6 个周期),3/4 级不良事件发生率相似(Gem/Cis-DEBIRI 组为 34%,Gem/Cis 组为 36%)。Gem/Cis-DEBIRI 组的总体缓解率在 2、4 和 6 个月时显著高于 Gem/Cis 组(p<0.04、p<0.03 和 p<0.05)。在 Gem/Cis-DEBIRI 组,与 Gem/Cis 组相比,有更多的肿瘤缩小到可切除/消融的程度(25%比 8%,p<0.05),无进展生存期也得到改善[31.9(95%CI 8.5-75.3)个月比 10.1(95%CI 5.3-13.5)个月,p=0.028],总生存期也得到改善[33.7(95%CI 13.5-54.5)个月比 12.6(95%CI 8.7-33.4)个月,p=0.048]。
Gem/Cis 联合 DEBIRI 是安全的,并导致肿瘤缩小到可切除程度的显著改善,无进展生存期和总生存期的改善。