Gupta Shipra Vinod, Jose Nadina, Tafuto Barbara
Department of Health Informatics, School of Health Professions, Rutgers, The State University of New Jersey, 65 Bergen Street, NJ 07107, United States.
Princ Pract Clin Res. 2024 Aug 3;10(2):47-59. doi: 10.21801/ppcrj.2024.102.7. Epub 2024 Sep 22.
Gilteritinib, an effective and selective inhibitor of the FLT3 gene, was developed to address the challenges posed by relapsed or refractory acute myeloid leukemia (AML) patients who often encounter limited treatment options and poor prognoses with salvage chemotherapy.
This systematic review aims to explore the progression of interventional research and consolidate existing evidence on the clinical effectiveness of gilteritinib as a monotherapy or combination therapy in improving overall survival among adults experiencing a recurrence or resistance to treatment for FLT3-positive AML patients.
A comprehensive search strategy, utilizing Medical Subject Headings (MeSH) and non-MeSH terms was conducted across Pubmed, EMBASE, Cochrane, and Web of Science databases. We primarily focused on the clinical trial and retrospective studies on gilteritinib as an intervention for relapsed/refractory AML patients.
According to our predefined criteria for inclusion and exclusion, we identified 3 published clinical trials and 5 retrospective studies focused on the overall response of gilteritinib on refractory or relapsed AML adult patients published between January 1, 2018, and March 25, 2024. Clinical trial studies demonstrated superior survival outcomes than salvage chemotherapy in the FLT3-positive AML population particularly showing higher efficacy in combination therapy with Azacitidine. Retrospective studies from clinical trials revealed improved clinical outcomes in AML sub-populations.
Gilteritinib exhibited promising outcomes by targeting FLT3 receptors, offering a new treatment approach, and revealing improved overall survival compared to salvage chemotherapy in the difficult-to-treat patient population.
吉瑞替尼是一种有效且选择性的FLT3基因抑制剂,旨在应对复发或难治性急性髓系白血病(AML)患者所面临的挑战,这些患者在挽救性化疗中往往治疗选择有限且预后不佳。
本系统评价旨在探讨干预性研究的进展,并整合现有证据,以证明吉瑞替尼作为单药治疗或联合治疗在改善FLT3阳性AML复发或耐药成年患者总体生存率方面的临床有效性。
采用医学主题词(MeSH)和非MeSH词,在PubMed、EMBASE、Cochrane和Web of Science数据库中进行全面检索。我们主要关注以吉瑞替尼作为复发/难治性AML患者干预措施的临床试验和回顾性研究。
根据我们预先设定的纳入和排除标准,我们确定了3项已发表的临床试验和5项回顾性研究,这些研究聚焦于2018年1月1日至2024年3月25日期间发表的吉瑞替尼对难治性或复发性AML成年患者的总体反应。临床试验研究表明,在FLT3阳性AML人群中,吉瑞替尼的生存结果优于挽救性化疗,尤其是与阿扎胞苷联合治疗时疗效更高。临床试验的回顾性研究显示AML亚组的临床结果有所改善。
吉瑞替尼通过靶向FLT3受体展现出了有前景的结果,提供了一种新的治疗方法,并且在难治性患者群体中与挽救性化疗相比显示出总体生存率的提高。