血管紧张素转换酶抑制剂对肌浸润性膀胱癌新辅助化疗病理完全反应的影响

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
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引用次数: 0

摘要

肾素-血管紧张素系统(RAS)已被证实可调节细胞增殖、脱屑、血管生成和免疫抑制。我们研究了RAS抑制剂(RASi)--即血管紧张素转换酶抑制剂(ACEi)和血管紧张素受体阻滞剂(ARB)--与根治性膀胱切除术(RC)前肌浸润性膀胱癌(MIBC)新辅助化疗(NAC)的关系。我们对来自 3 家学术机构的 302 名肌浸润性膀胱癌患者在根治性膀胱切除术前同时使用 RASi 和 NAC 的情况进行了回顾性调查。研究结果包括病理完全反应(pCR)和总生存率(OS)。研究人员收集了病理特征、表现状态(PS)、临床分期、NAC的类型/周期数以及毒性反应。总pCR率为26.2%,5年OS率为62%。同时服用 ACEi 和 NAC 与 pCR 的关系接近显著性(几率比 [OR] = 1.71; 95% CI, 0.94-3.11; = .077)。接受 ACEi 治疗的 cT3/4N0-N1 患者的 pCR 率(30.8% vs. 17.7%,= .056)高于未接受 ACEi 治疗的患者。女性性别与摄入 ACEi 的 pCR 交互作用具有统计学意义(= .044)。ACEi的摄入量与OS无关,而pCR、PS和较低的临床分期与OS的改善显著相关。摄入 ACEi 可能与在 RC 前接受 NAC 治疗的 MIBC 患者的 pCR 增加有关,这种关联在开始治疗时疾病临床分期较高且性别为女性的患者中更为明显。我们的数据表明,RAS 作为侵袭性 MIBC 的治疗靶点具有潜在的相关性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Impact of Angiotensin Converting Enzyme Inhibitors on Pathologic Complete Response With Neoadjuvant Chemotherapy for Muscle Invasive Bladder Cancer

Introduction

The renin-angiotensin system (RAS) has been demonstrated to modulate cell proliferation, desmoplasia, angiogenesis and immunosuppression. We examined the association of RAS inhibitors (RASi)—namely angiotensin converting enzyme inhibitors (ACEi) and angiotensin receptor blockers (ARB)—with neoadjuvant chemotherapy (NAC) for muscle-invasive bladder cancer (MIBC) preceding radical cystectomy (RC).

Patients and Methods

We retrospectively investigated concurrent RASi use with NAC prior to RC in 302 patients with MIBC from 3 academic institutions. Outcomes included pathologic complete response (pCR) and overall survival (OS). Pathologic features, performance status (PS), clinical stage, type/number of cycles of NAC, and toxicities were collected.

Results

Overall pCR rate was 26.2% and 5-year OS was 62%. Concurrent ACEi intake with NAC approached significance for association with pCR (odds ratio [OR] = 1.71; 95% CI, 0.94-3.11; P = .077). Patients with cT3/4N0-N1 disease receiving ACEi had higher pCR rates (30.8% vs. 17.7%, P = .056) than those not on ACEi. Female sex had a statistically significant favorable interaction for pCR with ACEi intake (P = .044). ACEi intake was not associated with OS, while pCR, PS and lower clinical stage were significantly associated with improved OS.

Conclusion

ACEi intake is potentially associated with increased pCR in patients with MIBC receiving NAC prior to RC, and this association is more pronounced in patients with higher clinical stage of disease at the initiation of therapy and female sex. Our data suggest the potential relevance of the RAS as a therapeutic target in aggressive MIBC.

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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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