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while good quality trials (often with larger group sizes) are stopped prematurely due to lack of effects and remain unpublished.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.
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。