Department of Gastrointestinal Oncology, H. Lee Moffitt Cancer Center, Tampa, Florida.
Department of Biostatistics and Bioinformatics, H. Lee Moffitt Cancer Center, Tampa, Florida.
Cancer. 2021 Apr 15;127(8):1293-1300. doi: 10.1002/cncr.33364. Epub 2020 Dec 8.
Biliary tract cancer (BTC) has a poor prognosis despite treatment with first-line gemcitabine and cisplatin. In BTC, PI3K/AKT pathway activation has been shown to increase resistance to chemotherapy, which may be overcome with PI3K inhibition. This phase 2 study evaluated the safety and efficacy of copanlisib, a PI3K inhibitor, with gemcitabine and cisplatin in advanced BTCs. The role of PTEN expression in outcomes was also explored.
Patients with advanced/unresectable BTC received gemcitabine, cisplatin, and copanlisib as their first-line treatment. The primary endpoint was progression-free survival (PFS) at 6 months. Secondary endpoints were the response rate (RR), median overall survival (OS)/PFS, and safety profile. An assessment of PTEN expression by immunohistochemistry was also performed along with molecular profiling.
Twenty-four patients received at least 1 dose of the study drug. The PFS rate at 6 months was 51%; the median OS was 13.7 months (95% CI, 6.8-18.0 months), and the median PFS was 6.2 months (95% CI, 2.9-10.1 months). Nineteen patients were evaluable for RR: 6 patients achieved a partial response (31.6%), and 11 (57.9%) had stable disease. The most common grade 3/4 adverse events were a decreased neutrophil count (45.83%), anemia (25%), increased lipase (25%), and hypertension (20.8%). Twenty patients had tissue evaluable for the PTEN status. The PFS for low (n = 9) and high PTEN expression (n = 11) was 8.5 and 4.6 months, respectively (P = .19). The median OS for low and high PTEN expression groups was 17.9 and 7.0 months, respectively (P = .19).
The addition of copanlisib to gemcitabine and cisplatin does not improve PFS at 6 months. However, future studies using PTEN as a potential biomarker should be considered.
The addition of copanlisib, a PI3K inhibitor, to standard chemotherapy for advanced biliary tract cancers was assessed for efficacy and safety. Twenty-four patients with advanced biliary tract cancer received treatment in this study. There was no difference in survival with the addition of copanlisib in comparison with standard chemotherapy. Copanlisib may be more effective and increase survival in patients with low PTEN expression levels. Further studies are needed to confirm this. No unexpected adverse events occurred.
尽管采用吉西他滨和顺铂进行一线治疗,胆道癌(BTC)的预后仍较差。在 BTC 中,已证实 PI3K/AKT 通路的激活会增加对化疗的耐药性,这可能可以通过抑制 PI3K 来克服。这项 2 期研究评估了在晚期 BTC 中,PI3K 抑制剂 copanlisib 与吉西他滨和顺铂联合应用的安全性和疗效。还探讨了 PTEN 表达在结果中的作用。
接受吉西他滨、顺铂和 copanlisib 作为一线治疗的晚期/不可切除 BTC 患者入组本研究。主要终点为 6 个月时的无进展生存期(PFS)。次要终点包括缓解率(RR)、中位总生存期(OS)/PFS 和安全性。还通过免疫组化评估了 PTEN 表达情况,并进行了分子谱分析。
24 例患者至少接受了 1 剂研究药物。6 个月时的 PFS 率为 51%;中位 OS 为 13.7 个月(95%CI,6.8-18.0 个月),中位 PFS 为 6.2 个月(95%CI,2.9-10.1 个月)。19 例患者可评估 RR:6 例患者获得部分缓解(31.6%),11 例(57.9%)为疾病稳定。最常见的 3/4 级不良事件为中性粒细胞计数降低(45.83%)、贫血(25%)、脂肪酶升高(25%)和高血压(20.8%)。20 例患者有组织可评估 PTEN 状态。低(n=9)和高(n=11)PTEN 表达患者的 PFS 分别为 8.5 和 4.6 个月(P=0.19)。低和高 PTEN 表达组的中位 OS 分别为 17.9 和 7.0 个月(P=0.19)。
与吉西他滨和顺铂相比,添加 copanlisib 并不能改善 6 个月时的 PFS。然而,应该考虑使用 PTEN 作为潜在的生物标志物进行进一步的研究。
评估了 PI3K 抑制剂 copanlisib 联合标准化疗治疗晚期胆道癌的疗效和安全性。24 例晚期胆道癌患者接受了这项研究的治疗。与标准化疗相比,添加 copanlisib 并未改善患者的生存。copanlisib 可能对低 PTEN 表达水平的患者更有效,并能提高其生存率。需要进一步的研究来证实这一点。未发生意外的不良事件。