Suppr超能文献

60岁以上骨髓增生异常综合征患者的继发性急性髓系白血病

Secondary Acute Myeloid Leukemia in Myelodysplastic Syndrome Patients Aged Over 60 Years.

作者信息

Chaudhuri Dipabali, Khan Kokab Irfan, Al Shouli Roba, Allakky Akhil, Ferguson Asila A, Khan Aujala Irfan, Abuzainah Baraa, Gutlapalli Sai Dheeraj, Hamid Pousette

机构信息

Research, California Institute of Behavioral Neurosciences & Psychology, Fairfield, USA.

Pediatrics, California Institute of Behavioral Neurosciences & Psychology, Fairfield, USA.

出版信息

Cureus. 2023 Jun 8;15(6):e40124. doi: 10.7759/cureus.40124. eCollection 2023 Jun.

Abstract

In myelodysplastic syndrome (MDS), neoplastic cells originate in hematopoietic stem cells of the bone marrow, causing dysplasia in multiple cell lines. This may ultimately lead to cytopenia and anemia. MDS generally occurs in patients aged over 60 years, and if left unchecked, it can lead to secondary acute myeloid leukemia (AML), which has a worse prognosis than de novo AML. Hence, it is important to find methods to treat and manage MDS and prevent secondary AML. This review tries to point out the best methods to find out the best possible treatment for MDS, which can lead to its remission or possibly cure and prevent it from progressing into AML. In order to do this, the pathogenesis of MDS is taken into account, and it is clear that the various molecular mutations that lead to the hematologic neoplasms directly affect the different chemotherapy agents that can be used. The different common mutations leading to MDS and secondary AML have been reviewed along with the drugs best inclined to target them. Some mutations lead to a worse prognosis than others, and ongoing mutations can lead to drug-resistant neoplasms. Thus, drugs targeting the mutations need to be used. The feasibility of an allogeneic stem cell transplant is also taken into account, as this can lead to a total cure of MDS. Methods of decreasing post-transplant recovery time and complications have been looked into, and more studies need to be done on the matter. Currently, it is clear that a more personalized approach to each individual case with its own set of drug combinations is the best approach to treating MDS and secondary leukemia and increasing the overall survival (OS).

摘要

在骨髓增生异常综合征(MDS)中,肿瘤细胞起源于骨髓造血干细胞,导致多系细胞发育异常。这最终可能导致血细胞减少和贫血。MDS通常发生在60岁以上的患者中,如果不加以控制,可能会导致继发性急性髓系白血病(AML),其预后比原发性AML更差。因此,找到治疗和管理MDS以及预防继发性AML的方法很重要。本综述试图指出找出MDS最佳治疗方法的最佳途径,这种方法可以使其缓解或可能治愈,并防止其进展为AML。为了做到这一点,考虑了MDS的发病机制,很明显导致血液肿瘤的各种分子突变直接影响可使用的不同化疗药物。已对导致MDS和继发性AML的不同常见突变以及最倾向于靶向它们的药物进行了综述。一些突变导致的预后比其他突变更差,持续的突变可导致肿瘤耐药。因此,需要使用针对这些突变的药物。还考虑了异基因干细胞移植的可行性,因为这可以使MDS完全治愈。已经研究了缩短移植后恢复时间和减少并发症的方法,对此还需要进行更多研究。目前,很明显针对每个病例采用更个性化的方法,使用其自己的一组药物组合,是治疗MDS和继发性白血病以及提高总生存期(OS)的最佳方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5668/10329419/94a425b6d795/cureus-0015-00000040124-i01.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验