Yasmin Farah, Moeed Abdul, Alam Muhammad Tanveer, Virwani Vikash, Khabir Yumna, Shaikh Asim, Vyas Apurva V, Alraies M Chadi
Yale University School of Medicine, New Haven, CT, 06511, USA.
Yale School of Medicine, New Haven, CT, 06511, USA.
Cardiooncology. 2024 Sep 12;10(1):61. doi: 10.1186/s40959-024-00265-7.
Clinical outcomes for TAVR in cancer survivors with prior chest radiation therapy (C-XRT) who develop symptomatic aortic-valve stenosis are not adequately assessed in major clinical trials leading to conflicting results. Hence, we conducted this meta-analysis to evaluate the, safety, efficacy, and mortality outcomes of cancer survivors with prior C-XRT undergoing TAVR. MEDLINE and Scopus were searched up to March 2024. Observational studies and randomized controlled trials comparing severe aortic stenosis patients with and without prior C-XRT undergoing TAVR with at least one outcome of interest were shortlisted. Data were analyzed using random-effects model to derive weighted mean differences, and risk ratios with 95% confidence intervals. Six studies with 6,191 patients (278 C-XRT and 5,913 no-C-XRT) were included. All-cause mortality at 30-day (RR 1.63, p = 0.12) and 1-year interval (RR 1.59, p = 0.08) showed no significant differences with prior C-XRT versus no-C-XRT. Worsening CHF was the only post-procedural safety outcome significantly higher in patients with prior C-XRT (RR 1.98, p = 0.0004) versus no- C-XRT. The efficacy end-points i.e., improvement in LVEF (MD 1.24; -0.50, 2.98), and aortic valve gradient (MD -0.63; -1.32, 0.05) were not significantly different. TAVR has similar all-cause mortality, efficacy and safety (except CHF worsening) among cancer survivors with and without a prior history of C-XRT.
在患有症状性主动脉瓣狭窄的曾接受胸部放疗(C-XRT)的癌症幸存者中,经导管主动脉瓣置换术(TAVR)的临床结局在主要临床试验中未得到充分评估,导致结果相互矛盾。因此,我们进行了这项荟萃分析,以评估曾接受C-XRT的癌症幸存者接受TAVR的安全性、有效性和死亡率结局。检索MEDLINE和Scopus截至2024年3月的数据。入选了比较曾接受和未接受C-XRT的重度主动脉瓣狭窄患者接受TAVR且至少有一项感兴趣结局的观察性研究和随机对照试验。使用随机效应模型分析数据,以得出加权平均差和95%置信区间的风险比。纳入了六项研究,共6191例患者(278例曾接受C-XRT,5913例未接受C-XRT)。有C-XRT与无C-XRT相比,30天(风险比1.63,p = 0.12)和1年时的全因死亡率无显著差异。心力衰竭恶化是曾接受C-XRT的患者术后唯一显著高于未接受C-XRT患者的安全性结局(风险比1.98,p = 0.0004)。有效性终点,即左心室射血分数改善(平均差1.24;-0.50,2.98)和主动脉瓣梯度(平均差-0.63;-1.32,0.05)无显著差异。在有和没有C-XRT病史的癌症幸存者中,TAVR的全因死亡率、有效性和安全性(心力衰竭恶化除外)相似。