Department of Internal Medicine, Detroit Medical Center, Wayne State University, Detroit, MI, USA.
Cancer Chemother Pharmacol. 2010 Aug;66(3):413-23. doi: 10.1007/s00280-010-1317-x. Epub 2010 Apr 8.
Bendamustine (Treanda, Ribomustin) is a water-soluble, bifunctional chemotherapeutic agent that also has potential antimetabolite properties and only partial cross-resistance with other alkylators. Designed in 1963 and re-discovered in 1990s, this drug's unique mechanism of action and favorable side-effect profile promise a major role in the management of lymphoproliferative disorders. Bendamustine has been designated as an orphan drug in the United States, conferring prolonged market exclusivity.
This article provides a comprehensive review of the data on efficacy and toxicity from trials investigating the use of bendamustine for the treatment of lymphoproliferative neoplasms. The pharmacology, pharmacokinetics, and pre-clinical studies with bendamustine are also reviewed.
MEDLINE and Pubmed databases (1970-2010) were searched using the terms bendamustine, bendamustin, Treanda, Ribomustin, SDX-105, IMET-3393, and Cytostasan. All relevant articles were reviewed and references screened for additional articles. The databases of the American Society of Hematology (2004-2009) and the American Society of Clinical Oncology (1995-2009) were also searched for relevant abstracts.
Bendamustine induces a remission in more than three-fourths of patients with rituximab-refractory indolent B cell non-Hodgkin lymphoma (NHL). Combined with rituximab in vitro, bendamustine shows synergistic effects against various leukemia and lymphoma cell lines. Clinical trials supporting these results show that bendamustine plus rituximab is highly effective in patients with relapsed-refractory indolent lymphoma, inducing remissions in 90% or more and a median progression-free survival of 23-24 months. Bendamustine has been reasonably well tolerated in clinical trials with low propensity to induce alopecia.
Combination of bendamustine and rituximab has the potential to become a new standard first-line treatment option for patients with FL, MCL, and indolent lymphomas. Results of ongoing trials will help to further elucidate the optimal role of bendamustine in indolent NHL.
苯达莫司汀(Treanda,Ribomustin)是一种水溶性的双功能化疗药物,具有潜在的抗代谢物特性,与其他烷化剂仅有部分交叉耐药性。该药物于 1963 年设计,并于 20 世纪 90 年代重新发现,其独特的作用机制和良好的副作用特征有望在淋巴增生性疾病的治疗中发挥重要作用。苯达莫司汀已被美国指定为孤儿药,享有长期的市场独占权。
本文全面综述了临床试验中苯达莫司汀治疗淋巴增生性肿瘤的疗效和毒性数据。同时还综述了苯达莫司汀的药理学、药代动力学和临床前研究。
使用苯达莫司汀、苯达莫司汀、Treanda、Ribomustin、SDX-105、IMET-3393 和 Cytostasan 等术语,在 MEDLINE 和 Pubmed 数据库(1970-2010 年)中进行检索。对所有相关文章进行了综述,并对参考文献进行了筛选,以获取其他文章。还对美国血液学会数据库(2004-2009 年)和美国临床肿瘤学会数据库(1995-2009 年)进行了检索,以获取相关摘要。
苯达莫司汀可使超过四分之三的利妥昔单抗难治性惰性 B 细胞非霍奇金淋巴瘤(NHL)患者获得缓解。体外联合利妥昔单抗,苯达莫司汀对多种白血病和淋巴瘤细胞系显示协同作用。支持这些结果的临床试验表明,苯达莫司汀联合利妥昔单抗在复发性难治性惰性淋巴瘤患者中非常有效,可使 90%以上的患者获得缓解,中位无进展生存期为 23-24 个月。苯达莫司汀在临床试验中耐受性良好,不易引起脱发。
苯达莫司汀联合利妥昔单抗有可能成为 FL、MCL 和惰性淋巴瘤患者的新一线治疗选择。正在进行的试验结果将有助于进一步阐明苯达莫司汀在惰性 NHL 中的最佳作用。