Podar Klaus, Tai Yu-Tzu, Hideshima Teru, Vallet Sonia, Richardson Paul G, Anderson Kenneth C
Dana-Farber Cancer Institute, Jerome Lipper Multiple Myeloma Center, Department of Medical Oncology, Boston, MA 02115, USA.
Expert Opin Emerg Drugs. 2009 Mar;14(1):99-127. doi: 10.1517/14728210802676278.
Multiple myeloma (MM) is a clonal plasma cell malignancy clinically characterized by osteolytic lesions, immunodeficiency, and renal disease. There are an estimated 750,000 people diagnosed with MM worldwide, with a median overall survival of 3 - 5 years. Besides chromosomal aberrations, translocations, and mutations in essential growth and tumor-suppressor genes, accumulating data strongly highlight the pathophysiologic role of the bone marrow (BM) microenvironment in MM pathogenesis. Based on this knowledge, several novel agents have been identified, and treatment options in MM have fundamentally changed during the last decade. Thalidomide, bortezomib, and lenalidomide have been incorporated into conventional cytotoxic and transplantation regimens, first in relapsed and refractory and now also in newly diagnosed MM. Despite these significant advances, there remains an urgent need for more efficacious and tolerable drugs. Indeed, a plethora of preclinical agents awaits translation from the bench to the bedside. This article reviews the scientific rationale of new therapy regimens and newly identified therapeutic agents - small molecules as well as therapeutic antibodies - that hold promise to further improve outcome in MM.
多发性骨髓瘤(MM)是一种克隆性浆细胞恶性肿瘤,临床特征为溶骨性病变、免疫缺陷和肾脏疾病。据估计,全球有75万人被诊断为MM,总体中位生存期为3至5年。除了染色体畸变、易位以及关键生长和肿瘤抑制基因的突变外,越来越多的数据强烈凸显了骨髓(BM)微环境在MM发病机制中的病理生理作用。基于这一认识,已经确定了几种新型药物,并且在过去十年中MM的治疗选择发生了根本性变化。沙利度胺、硼替佐米和来那度胺已被纳入传统的细胞毒性和移植方案中,最初用于复发和难治性MM,现在也用于新诊断的MM。尽管取得了这些重大进展,但仍迫切需要更有效且耐受性更好的药物。确实,大量临床前药物正等待从实验室转化到临床应用。本文综述了有望进一步改善MM治疗效果的新治疗方案以及新确定的治疗药物——小分子药物和治疗性抗体——的科学依据。