Zheng Lu, Tan Jun, Yan Yi, Wang Shang, Yuan Ping, Wu Cheng, Zhao Yin-Tao, Yang Hai-Bo, Nappi Francesco, Tonelli Adriano R, Wang Lan, Hu Qing-Hua, Jiang Rong
Department of Cardiology, the First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Department of Critical Care Medicine, Yeda Hospital of Yantai, Yantai, China.
J Thorac Dis. 2023 Jun 30;15(6):3372-3385. doi: 10.21037/jtd-23-701. Epub 2023 Jun 19.
Data are quite sparse on the comprehensive analyses of pulmonary hypertension (PH) clinical trials worldwide.
Information including participating countries (developed or developing), intervention type, trial size, PH categories, sponsorship, study phase, design strategies, and participants' demographic characteristics was extracted from PH trials registered on ClinicalTrials.gov from 1999 to 2021.
A total of 203 eligible clinical PH trials were screened, involving 23,402 participants, 67.8% of whom were females. Major clinical trials were designed to test drug interventions (95.6%), sponsored solely by industries in 59.5%, and targeting Group 1 PH patients in 76.3%. A large number of countries participated in PH clinical trials; however, most clinical trials were conducted in developed countries (84.2%). Developing countries were involved in clinical trials with larger sample sizes (P<0.01). Additionally, the differences between developed and developing countries centered on interventions, sponsors, PH groups, and design strategies. Furthermore, developing countries participated in multinational clinical trials with good quality, homogeneity, reliability, and data authenticity. All pediatric participants were diagnosed with Group 1 PH and were only involved in drug intervention trials. Children participated in far fewer clinical trials than adults (P<0.01), and most were enrolled in PH clinical trials in developed countries. Among the entire clinical trial population, younger patients with Group 1 PH had a much higher participation to prevalence ratio (PPR). There was no difference in women's PPRs between developed and developing countries. However, developing countries had higher PPRs for PH Groups I and IV (1.28 . 1.22, P<0.01), while developed countries had a lower PPR for Group III (P=0.02).
PH is attracting increasing global attention, which is not at the same level of progress in developed and developing countries. Women and children with this disease have unique characteristics and require more attention.
关于全球肺动脉高压(PH)临床试验的综合分析数据相当稀少。
从1999年至2021年在ClinicalTrials.gov上注册的PH试验中提取包括参与国家(发达国家或发展中国家)、干预类型、试验规模、PH类别、赞助情况、研究阶段、设计策略以及参与者人口统计学特征等信息。
共筛选出203项符合条件的临床PH试验,涉及23402名参与者,其中67.8%为女性。主要临床试验旨在测试药物干预(95.6%),59.5%仅由行业赞助,76.3%针对1组PH患者。大量国家参与了PH临床试验;然而,大多数临床试验在发达国家进行(84.2%)。发展中国家参与了样本量更大的临床试验(P<0.01)。此外,发达国家和发展中国家之间的差异集中在干预措施、赞助商、PH组和设计策略上。此外,发展中国家参与了质量良好、同质性高、可靠性强且数据真实性高的跨国临床试验。所有儿科参与者均被诊断为1组PH,且仅参与药物干预试验。儿童参与的临床试验比成人少得多(P<0.01),且大多数儿童在发达国家的PH临床试验中入组。在整个临床试验人群中,1组PH的年轻患者参与率与患病率之比(PPR)要高得多。发达国家和发展中国家女性的PPR没有差异。然而,发展中国家1组和4组PH的PPR较高(分别为1.28和1.22,P<0.01),而发达国家3组的PPR较低(P=0.02)。
PH正吸引着全球越来越多的关注,发达国家和发展中国家在这方面的进展水平不同。患有这种疾病的妇女和儿童具有独特特征,需要更多关注。