Department of Oncology, Medical University of Warsaw, 02-091, Warsaw, Poland.
Department of Molecular Biology, Institute of Genetics and Animal Biotechnology, Polish Academy of Sciences, 05-552, Garbatka, Poland.
J Cancer Res Clin Oncol. 2024 Sep 28;150(9):434. doi: 10.1007/s00432-024-05962-5.
Pancreatic cancer remains a significant public health challenge, with poor long-term outcomes due to the lack of effective treatment options. Repurposing commonly used clinical drugs, such as ACE inhibitors, ARBs, CCBs, and metformin, may enhance the efficacy of chemotherapy and offer a promising therapeutic strategy for improving patient outcomes.
A retrospective analysis of concomitant treatment with ACE-Is, ARBs, CCBs, and metformin alongside gemcitabine chemotherapy in patients with pancreatic cancer was conducted. Treatment responses were evaluated, with overall survival (OS) estimated using the Kaplan-Meier method. Additionally, the Cox proportional hazards model was employed to assess the impact of these specific agents on patient survival.
4628 patients with various stages of pancreatic cancer were identified in the database between 2007 and 2016. The estimated overall survival (OS) in the analyzed group was 6.9 months (95% CI 6.4-7). The use of any of the analyzed drugs was associated with a significant improvement in mOS of 7.5 months (95% CI 6.8-7.8) vs. 6.7 months (95% CI 6.4-7.0) for patients who did not have additional treatment (p < 0.0001). ARBs, ACE-Is, CCBs, and metformin varied in their effectiveness in prolonging mOS among patients. The longest mOS of 8.9 months (95% CI 7.7-11.6) was observed in patients receiving additional therapy with ARBs, while the shortest mOS of 7.7 months (95% CI 6.5-8.9) was achieved by patients receiving metformin. In the adjusted Cox analysis, metformin was associated with a significantly weaker effect on mOS (p = 0.029). A particularly interesting trend in prolonging 5-year survival was demonstrated by ARBs and CCBs with 14.1% (95% CI 9-22%) and 14.8% (95% CI 11.1-19.6%), respectively, compared to patients not taking these drugs, who achieved a 5-year OS of 3.8% (95% CI 3.2-4.4%).
Our results demonstrate a significant positive impact of ARBs, ACE inhibitors, and CCBs on survival in patients with pancreatic cancer treated with gemcitabine. The addition of these inexpensive and relatively safe drugs in patients with additional comorbidities may represent a potential therapeutic option in this indication. However, prospective clinical trials to evaluate the optimal patient population and further studies to determine the potential impact of these agents on chemotherapy are necessary.
由于缺乏有效的治疗选择,胰腺癌仍然是一个重大的公共健康挑战,导致长期预后不佳。重新利用常用的临床药物,如 ACE 抑制剂、ARB、CCB 和二甲双胍,可能会增强化疗的疗效,并为改善患者预后提供有前途的治疗策略。
对 2007 年至 2016 年间数据库中接受吉西他滨化疗的同时接受 ACE-Is、ARB、CCB 和二甲双胍联合治疗的胰腺癌患者进行回顾性分析。评估治疗反应,使用 Kaplan-Meier 方法估计总生存期(OS)。此外,还采用 Cox 比例风险模型评估这些特定药物对患者生存的影响。
在数据库中确定了 4628 名患有各种阶段胰腺癌的患者。在分析组中,估计的总生存期(OS)为 6.9 个月(95%CI 6.4-7)。与未接受额外治疗的患者(95%CI 6.4-7.0)相比,使用任何一种分析药物均可显著改善 mOS,达到 7.5 个月(95%CI 6.8-7.8)(p<0.0001)。ARB、ACE-Is、CCB 和二甲双胍在延长 mOS 方面的有效性在患者中有所不同。在接受 ARB 额外治疗的患者中,mOS 最长为 8.9 个月(95%CI 7.7-11.6),而接受二甲双胍治疗的患者 mOS 最短为 7.7 个月(95%CI 6.5-8.9)。在调整后的 Cox 分析中,二甲双胍对 mOS 的影响明显较弱(p=0.029)。ARB 和 CCB 在延长 5 年生存率方面表现出特别有趣的趋势,与未服用这些药物的患者相比,5 年 OS 分别为 14.1%(95%CI 9-22%)和 14.8%(95%CI 11.1-19.6%),后者的 5 年 OS 为 3.8%(95%CI 3.2-4.4%)。
我们的结果表明,ARB、ACE 抑制剂和 CCB 对接受吉西他滨治疗的胰腺癌患者的生存有显著的积极影响。在有额外合并症的患者中添加这些廉价且相对安全的药物可能是该适应症的一种潜在治疗选择。然而,需要进行前瞻性临床试验来评估最佳患者人群,并进一步研究这些药物对化疗的潜在影响。