Therapeutic angiogenesis for patients with chronic limb-threatening ischemia: promising or hoax?

Vascular biology (Bristol, England) Pub Date : 2024-11-08 Print Date: 2024-01-01 DOI:10.1530/VB-24-0009
Judith A H M Peeters, Abbey Schepers, Jaap F Hamming, Paul H A Quax
{"title":"Therapeutic angiogenesis for patients with chronic limb-threatening ischemia: promising or hoax?","authors":"Judith A H M Peeters, Abbey Schepers, Jaap F Hamming, Paul H A Quax","doi":"10.1530/VB-24-0009","DOIUrl":null,"url":null,"abstract":"<p><p>Chronic limb-threatening ischemia (CLTI) is a critical end-stage disease that leads to high amputation rates. Over the past few decades, therapeutic angiogenesis has attracted a lot of attention as a means to reduce the necessity for amputations. Especially gene- and cell therapy are regarded to as possible treatment modalities to restore the hampered blood flow. So far, early-phase clinical trials often fail to prove a significant clinical improvement in mortality, amputation rate, and ulcer healing but still conclude that therapeutic angiogenesis might be promising as therapy. The subsequent phase III clinical trials based on these indecisive early trials fail consistently to demonstrate clinical benefits leaving the promising early results unvalidated. In this review we will illustrate that designing good trials for CLTI patients is challenging, not in the last place since patients are often not eligible due to strict inclusion criteria. Moreover, in this review, we advocate that clinical trials should be conducted with a low risk of bias and that it is of utmost importance to publish results, regardless of the outcome. It is definitely very concerning that many studies of a lower quality (due to small group size or high chance for bias) reporting positive outcomes are published while good quality trials (often with larger group sizes) are stopped prematurely due to lack of effects and remain unpublished. This keeps the 'promising but not yet proven' image of these therapeutic neovascularization studies alive, with still new groups starting similar trials.</p>","PeriodicalId":75294,"journal":{"name":"Vascular biology (Bristol, England)","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-11-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11623260/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Vascular biology (Bristol, England)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1530/VB-24-0009","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/1/1 0:00:00","PubModel":"Print","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Chronic limb-threatening ischemia (CLTI) is a critical end-stage disease that leads to high amputation rates. Over the past few decades, therapeutic angiogenesis has attracted a lot of attention as a means to reduce the necessity for amputations. Especially gene- and cell therapy are regarded to as possible treatment modalities to restore the hampered blood flow. So far, early-phase clinical trials often fail to prove a significant clinical improvement in mortality, amputation rate, and ulcer healing but still conclude that therapeutic angiogenesis might be promising as therapy. The subsequent phase III clinical trials based on these indecisive early trials fail consistently to demonstrate clinical benefits leaving the promising early results unvalidated. In this review we will illustrate that designing good trials for CLTI patients is challenging, not in the last place since patients are often not eligible due to strict inclusion criteria. Moreover, in this review, we advocate that clinical trials should be conducted with a low risk of bias and that it is of utmost importance to publish results, regardless of the outcome. It is definitely very concerning that many studies of a lower quality (due to small group size or high chance for bias) reporting positive outcomes are published while good quality trials (often with larger group sizes) are stopped prematurely due to lack of effects and remain unpublished. This keeps the 'promising but not yet proven' image of these therapeutic neovascularization studies alive, with still new groups starting similar trials.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
慢性肢体缺血患者的治疗性血管生成:有希望还是骗局?
慢性肢体缺血(CLTI)是一种严重的终末期疾病,导致截肢率居高不下。在过去几十年里,治疗性血管生成作为一种减少截肢必要性的手段引起了广泛关注。尤其是基因和细胞疗法被认为是恢复受阻血流的可能治疗方式。迄今为止,早期阶段的临床试验往往无法证明在死亡率、截肢率和溃疡愈合方面有明显的临床改善,但仍得出了治疗性血管生成可能是一种有前途的疗法的结论。在这些犹豫不决的早期试验基础上,随后进行的 III 期临床试验也始终无法证明临床疗效,使早期的乐观结果无法得到验证。在这篇综述中,我们将说明为CLTI患者设计良好的试验是一项挑战,而不是最后一项挑战,因为患者往往因严格的纳入标准而不符合条件。此外,在这篇综述中,我们主张临床试验应在低偏倚风险的情况下进行,而且无论结果如何,公布结果都是最重要的。令人十分担忧的是,许多质量较低的研究(由于群体规模较小或偏倚几率较高)报告了积极的结果,而质量较好的试验(通常群体规模较大)却因缺乏效果而过早停止,一直未被发表。这使得这些治疗性新生血管研究的 "前景光明但尚未得到证实 "的形象毫无必要地继续存在,而且仍有新的研究小组开始进行类似的试验。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
审稿时长
13 weeks
期刊最新文献
Lack of intracranial atherosclerosis in various atherosclerotic mouse models. Protection of liver sinusoidal endothelial cells using different preservation solutions. Therapeutic angiogenesis for patients with chronic limb-threatening ischemia: promising or hoax? Whole-body insulin resistance leads to accelerated atherosclerosis: role for Nox2 NADPH oxidase. Ang II-induced contraction is impaired in the aortas of renovascular hypertensive animal model.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1