Myeloma and MGUS

Matthew J Streetly
{"title":"Myeloma and MGUS","authors":"Matthew J Streetly","doi":"10.1016/j.mpmed.2025.02.010","DOIUrl":null,"url":null,"abstract":"<div><div>Plasma cell disorders result from a clonal proliferation of bone marrow plasma cells and range from benign monoclonal gammopathy of undetermined significance (MGUS) to malignant myeloma. Serum or urine monoclonal protein is usually detectable. MGUS is asymptomatic but can progress to myeloma or lymphoma. Myeloma is generally a disease of elderly individuals and presents with variable problems including anaemia, bone pain, fractures, spinal cord compression, renal failure, hypercalcaemia, recurrent infections and hyperviscosity. Diagnosis is based on bone marrow examination, and prognosis is influenced by specific acquired genetic abnormalities. Treatment is required after the development of, or to reduce the risk of developing, myeloma-related organ or tissue impairment. Myeloma is incurable, and treatment combines anti-myeloma chemoimmunotherapy with supportive therapies. Younger, medically fit patients are treated with intensive regimens combining chemotherapy with an autologous stem cell transplant, whereas older patients with co-morbidities and poorer performance status are generally offered less intensive treatment. It has a responding–relapsing disease course with eventual development of drug resistance. However, newer therapy options alone or in combination have improved outcomes in myeloma.</div></div>","PeriodicalId":74157,"journal":{"name":"Medicine (Abingdon, England : UK ed.)","volume":"53 5","pages":"Pages 325-330"},"PeriodicalIF":0.0000,"publicationDate":"2025-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Medicine (Abingdon, England : UK ed.)","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1357303925000441","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Plasma cell disorders result from a clonal proliferation of bone marrow plasma cells and range from benign monoclonal gammopathy of undetermined significance (MGUS) to malignant myeloma. Serum or urine monoclonal protein is usually detectable. MGUS is asymptomatic but can progress to myeloma or lymphoma. Myeloma is generally a disease of elderly individuals and presents with variable problems including anaemia, bone pain, fractures, spinal cord compression, renal failure, hypercalcaemia, recurrent infections and hyperviscosity. Diagnosis is based on bone marrow examination, and prognosis is influenced by specific acquired genetic abnormalities. Treatment is required after the development of, or to reduce the risk of developing, myeloma-related organ or tissue impairment. Myeloma is incurable, and treatment combines anti-myeloma chemoimmunotherapy with supportive therapies. Younger, medically fit patients are treated with intensive regimens combining chemotherapy with an autologous stem cell transplant, whereas older patients with co-morbidities and poorer performance status are generally offered less intensive treatment. It has a responding–relapsing disease course with eventual development of drug resistance. However, newer therapy options alone or in combination have improved outcomes in myeloma.
骨髓瘤和MGUS
浆细胞疾病是由骨髓浆细胞的克隆性增殖引起的,范围从良性单克隆性γ病(MGUS)到恶性骨髓瘤。血清或尿液单克隆蛋白通常可检测到。MGUS无症状,但可发展为骨髓瘤或淋巴瘤。骨髓瘤通常是老年人的疾病,表现为各种问题,包括贫血、骨痛、骨折、脊髓压迫、肾功能衰竭、高钙血症、复发性感染和高粘稠度。诊断基于骨髓检查,预后受特定获得性遗传异常的影响。在发生骨髓瘤相关器官或组织损伤后,或为降低发生骨髓瘤相关器官或组织损伤的风险,需要进行治疗。骨髓瘤是无法治愈的,治疗结合抗骨髓瘤化学免疫疗法与支持疗法。年轻的、医学上适合的患者采用化疗联合自体干细胞移植的强化方案进行治疗,而有合并症和表现较差的老年患者通常给予较少的强化治疗。它有一个反应复发的疾病过程,最终发展为耐药性。然而,新的治疗方案单独或联合治疗可改善骨髓瘤的预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
1.10
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信