Suppr超能文献

骨髓增殖性肿瘤治疗的新进展:当前和未来治疗选择的综述。

New Horizons in Myeloproliferative Neoplasms Treatment: A Review of Current and Future Therapeutic Options.

机构信息

Hematology Unit, Azienda Unità Sanitaria Locale-IRCCS, 42123 Reggio Emilia, Italy.

Ph.D. Program in Clinical and Experimental Medicine, University of Modena and Reggio Emilia, 42121 Modena, Italy.

出版信息

Medicina (Kaunas). 2021 Oct 31;57(11):1181. doi: 10.3390/medicina57111181.

Abstract

Philadelphia-negative myeloproliferative neoplasms (MPN) are aggressive diseases characterized by clonal proliferation of myeloid stem cells. The clonal process leads to excessive red cells production, platelets production, and bone marrow fibrosis. According to the phenotype, MPN can be classified as polycythemia vera (PV), essential thrombocythemia (ET), and primary myelofibrosis (PMF). MPN patients have shortened survival due to the increased risk of thrombosis, hemorrhages, and transformation to acute myeloid leukemia (AML). Prognosis is variable, with a shorter life expectancy in myelofibrosis. Currently, drug therapy can reduce symptoms, splenomegaly, and risk of thrombosis. Still, some patients can be resistant or intolerant to the treatment. At the same time, allogeneic stem cell transplant (ASCT) is the only treatment modality with the potential to cure the disease. Nevertheless, the ASCT is reserved for high-risk leukemic progression patients due to the risk of treatment-related death and comorbidity. Therefore, there is a need for new drugs that can eradicate clonal hematopoiesis and prevent progression to more aggressive myeloid neoplasms. Thanks to the better understanding of the disease's molecular pathogenesis, many new potentially disease-modifying drugs have been developed and are currently in clinical trials. This review explores the most promising new drugs currently in clinical trials.

摘要

费城阴性骨髓增殖性肿瘤(MPN)是一种侵袭性疾病,其特征为髓系干细胞的克隆性增殖。克隆过程导致过多的红细胞生成、血小板生成和骨髓纤维化。根据表型,MPN 可分为真性红细胞增多症(PV)、原发性血小板增多症(ET)和原发性骨髓纤维化(PMF)。由于血栓形成、出血和转化为急性髓系白血病(AML)的风险增加,MPN 患者的生存率缩短。预后各不相同,骨髓纤维化的预期寿命更短。目前,药物治疗可以减轻症状、脾肿大和血栓形成的风险。尽管如此,一些患者可能对治疗产生耐药性或不耐受。同时,异基因造血干细胞移植(ASCT)是唯一有治愈疾病潜力的治疗方法。然而,由于治疗相关死亡和合并症的风险,ASCT 仅保留给白血病进展风险高的患者。因此,需要新的药物来根除克隆性造血并预防向更具侵袭性的髓系肿瘤进展。由于对疾病分子发病机制的更好理解,许多新的潜在疾病修饰药物已经开发出来,并正在临床试验中。本综述探讨了目前临床试验中最有前途的新药。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6acd/8619471/dc97b95ab407/medicina-57-01181-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验