Saad Ayman A, Sharma Manish, Higa Gerald M
Section of Neoplastic Diseases and Related Disorders, Department of Internal Medicine, Medical College of Wisconsin, Milwaukee, WI, USA.
Ann Pharmacother. 2009 Feb;43(2):329-38. doi: 10.1345/aph.1L428. Epub 2009 Feb 3.
To review the clinical trials that have impacted treatment standards of multiple myeloma (MM).
A PubMed search (1980-June 2008) restricted to English-language publications was conducted using the key words multiple myeloma, clinical trials, targeted therapy, thalidomide, lenalidomide, bortezomib, dexamethasone, melphalan, autologous stem-cell transplantation, and tumor biology. Abstracts emanating from the meetings of the American Society of Clinical Oncology and American Society of Hematology from June 2002 to June 2008 were also reviewed.
Although hematopoietic stem-cell transplantation has improved the response rate and duration of overall survival, MM remains an incurable disease. However, focused research aimed at the molecular basis of the disease has led to a number of new treatment strategies. Evidence from clinical trials indicates that each of the 3 novel agents, thalidomide, lenalidomide, and bortezomib, is remarkably effective as first-line therapy. The data also suggest that clinicians may need to reevaluate the role of stem-cell transplantation in the disease.
Thalidomide, lenalidomide, or bortezomib in combination with dexamethasone have replaced traditional chemotherapy such as melphalan, doxorubicin, and vincristine as initial therapy of patients with MM who are eligible for stem-cell transplantation. Furthermore, these novel drugs can be incorporated into regimens used to treat transplant-ineligible patients or those with relapsing disease.
回顾影响多发性骨髓瘤(MM)治疗标准的临床试验。
使用关键词“多发性骨髓瘤”“临床试验”“靶向治疗”“沙利度胺”“来那度胺”“硼替佐米”“地塞米松”“美法仑”“自体干细胞移植”和“肿瘤生物学”,对PubMed数据库(1980年 - 2008年6月)进行检索,检索范围限定为英文出版物。同时也回顾了2002年6月至2008年6月美国临床肿瘤学会和美国血液学会会议的摘要。
尽管造血干细胞移植提高了缓解率和总生存期,但MM仍然是一种无法治愈的疾病。然而,针对该疾病分子基础的重点研究已产生了一些新的治疗策略。临床试验证据表明,沙利度胺、来那度胺和硼替佐米这三种新型药物作为一线治疗均非常有效。数据还表明临床医生可能需要重新评估干细胞移植在该疾病中的作用。
沙利度胺、来那度胺或硼替佐米联合地塞米松已取代传统化疗药物(如美法仑、阿霉素和长春新碱),成为适合干细胞移植的MM患者的初始治疗方案。此外,这些新型药物可纳入用于治疗不适合移植患者或复发疾病患者的治疗方案中。