来那度胺
多发性骨髓瘤
不确定意义的单克隆抗体病
医学
内科学
恶性肿瘤
地塞米松
无症状的
肿瘤科
胃肠病学
单克隆
免疫学
抗体
单克隆抗体
作者
S. Vincent Rajkumar,Shaji Kumar,Sagar Lonial,María‐Victoria Mateos
标识
DOI:10.1038/s41408-022-00719-0
摘要
Smoldering multiple myeloma (SMM) is an asymptomatic condition that occupies a space between monoclonal gammopathy of undetermined significance (MGUS) and multiple myeloma (MM) along the spectrum of clonal plasma cell proliferative disorders. It is not a biologic intermediate stage between MGUS and MM, but rather represents a heterogeneous clinically defined condition in which some patients (approximately two-thirds) have MGUS (pre-malignancy), and some (approximately one-third) have MM (biologic malignancy). Unfortunately, no single pathologic or molecular feature can reliably distinguish these two groups of patients. For purposes of practice and clinical trials, specific risk factors are used to identify patients with SMM in whom malignant transformation has already likely occurred (high risk SMM). Patients with newly diagnosed high risk SMM should be offered therapy with lenalidomide or lenalidomide plus dexamethasone (Rd) for 2 years, or enrollment in clinical trials. Patients with low risk SMM should be observed without therapy every 3-4 months.
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