Neparidze Natalia, Dhodapkar Madhav V
Yale University, New Haven, CT 06510, USA.
Clin Adv Hematol Oncol. 2009 Oct;7(10):677-81, 687-90.
Waldenstrom's macroglobulinemia (WM) is a B-cell disorder characterized by bone marrow infiltration with clonal lymphoplasmacytic cells (LPCs), along with an immunoglobulin M monoclonal gammopathy. Recent studies have led to several insights into disease biology as well as the development of an international staging system. Patients with asymptomatic macroglobulinemia should be observed without therapy. Options for frontline therapy include alkylating agents, nucleoside analogs, and rituximab, either as monotherapy or in combination. Although objective responses are common, complete remissions are infrequent. Several novel agents including proteasome inhibitors and thalidomide, as well as high-dose chemotherapy and stem cell transplantation are being incorporated into the therapeutic armamentarium in WM and show promising activity. This report provides an update on recent advances in biology and treatment of this disease.
华氏巨球蛋白血症(WM)是一种B细胞疾病,其特征为骨髓被克隆性淋巴浆细胞(LPC)浸润,并伴有免疫球蛋白M单克隆丙种球蛋白病。最近的研究对疾病生物学有了一些深入了解,并促成了国际分期系统的发展。无症状巨球蛋白血症患者应进行观察而不给予治疗。一线治疗方案包括烷化剂、核苷类似物和利妥昔单抗,可单独使用或联合使用。虽然客观缓解很常见,但完全缓解并不常见。包括蛋白酶体抑制剂和沙利度胺在内的几种新型药物,以及大剂量化疗和干细胞移植正被纳入WM的治疗手段中,并显示出有前景的活性。本报告提供了关于该疾病生物学和治疗方面最新进展的最新情况。