Adis, a Wolters Kluwer Business, Auckland, New Zealand.
Drugs. 2010 Sep 10;70(13):1703-18. doi: 10.2165/11205860-000000000-00000.
Bendamustine (bendamustine hydrochloride) is an alkylating agent indicated in several countries for the treatment of indolent non-Hodgkin's lymphoma (NHL) and mantle cell lymphoma (MCL). While the precise mechanism of action of bendamustine is as yet unknown, it has limited cross resistance to other alkylating agents and appears to exert its antineoplastic effects via a different mechanism to that of other alkylating agents. Bendamustine monotherapy was effective in treatment-refractory (including rituximab-refractory) indolent NHL or MCL. Moreover, bendamustine-based combination treatment was at least as effective as cyclophosphamide-based treatment, and bendamustine plus rituximab was at least as effective as cyclophosphamide, doxorubicin, vincristine plus prednisone (CHOP) plus rituximab, as first-line therapy in patients with indolent NHL or MCL. Treatment-refractory disease also appeared to respond favourably to bendamustine-containing combination treatment. In general, bendamustine was associated with a high overall response rate and a durable response. The most common adverse events associated with bendamustine were haematological or gastrointestinal in nature, and most were of mild to moderate severity. Regimens that included bendamustine were also associated with a very low rate of alopecia compared with regimens that included other antineoplastic drugs. In conclusion, bendamustine is a unique alkylating agent, which in clinical trials has demonstrated consistent efficacy and acceptable tolerability in patients with indolent NHL or MCL. It may be a particularly useful treatment option in patients with rituximab-refractory disease, but has also demonstrated efficacy as part of a first-line combination treatment. While further research is necessary to firmly establish the best place for bendamustine in the management of indolent NHL and MCL, it is a valuable addition to the pool of available treatments for these diseases.
苯达莫司汀(盐酸苯达莫司汀)是一种烷化剂,在多个国家被批准用于治疗惰性非霍奇金淋巴瘤(NHL)和套细胞淋巴瘤(MCL)。尽管苯达莫司汀的确切作用机制尚不清楚,但它与其他烷化剂的交叉耐药性有限,并且似乎通过与其他烷化剂不同的机制发挥其抗肿瘤作用。苯达莫司汀单药治疗难治性(包括利妥昔单抗难治性)惰性 NHL 或 MCL 有效。此外,苯达莫司汀联合治疗至少与环磷酰胺治疗一样有效,苯达莫司汀联合利妥昔单抗至少与环磷酰胺、多柔比星、长春新碱加泼尼松(CHOP)联合利妥昔单抗一样有效,作为惰性 NHL 或 MCL 患者的一线治疗。难治性疾病似乎也对含苯达莫司汀的联合治疗有良好的反应。总的来说,苯达莫司汀与高总缓解率和持久缓解相关。与苯达莫司汀相关的最常见不良事件是血液学或胃肠道性质的,大多数为轻度至中度严重程度。与包括其他抗肿瘤药物的方案相比,包括苯达莫司汀的方案也与极低的脱发率相关。总之,苯达莫司汀是一种独特的烷化剂,在临床试验中已证明在惰性 NHL 或 MCL 患者中具有一致的疗效和可接受的耐受性。它可能是利妥昔单抗难治性疾病患者的特别有用的治疗选择,但作为一线联合治疗的一部分也显示出疗效。虽然需要进一步的研究来确定苯达莫司汀在惰性 NHL 和 MCL 治疗中的最佳位置,但它是这些疾病现有治疗方法的宝贵补充。