Pönisch Wolfram, Niederwieser Dietger
East German Study Group for Hematology and Oncology (OSHO), University of Leipzig, Philipp Rosenthalstrasse 23-25, D-4103 Liepzig, Germany.
Semin Oncol. 2002 Aug;29(4 Suppl 13):23-6. doi: 10.1053/sonc.2002.34876.
Multiple myeloma (MM) is a malignancy of terminally differentiated plasma cells typically occurring in elderly patients. The clinical manifestations of this disease result primarily from the accumulation of monoclonal protein (paraprotein) in the serum and/or urine, anemia, lytic bone lesions, hypercalcemia, renal insufficiency, and immune deficiency. Multiple myeloma is incurable with standard chemotherapy. Melphalan and prednisone has been the mainstay of treatment for MM for about three decades. This regimen results in a clinical response in approximately 60% of patients and a median survival of approximately 36 months. A variety of combination therapies have also been used in MM, but have not been considered to offer a significant benefit compared with standard therapy. In early trials, bendamustine monotherapy was as effective as cyclophosphamide and various combination therapies in achieving remission in MM. This article describes a prospective, randomized, phase III study designed to compare the efficacy of bendamustine/prednisolone with a standard melphalan/prednisolone regimen.
多发性骨髓瘤(MM)是一种终末分化浆细胞的恶性肿瘤,通常发生于老年患者。该疾病的临床表现主要源于血清和/或尿液中单克隆蛋白(副蛋白)的蓄积、贫血、溶骨性骨病变、高钙血症、肾功能不全及免疫缺陷。标准化疗无法治愈多发性骨髓瘤。美法仑和泼尼松一直是治疗MM约三十年的主要方案。该方案使约60%的患者产生临床反应,中位生存期约为36个月。多种联合疗法也已用于MM,但与标准疗法相比,未被认为能带来显著益处。在早期试验中,苯达莫司汀单药治疗在使MM达到缓解方面与环磷酰胺及各种联合疗法效果相当。本文描述了一项前瞻性、随机、III期研究,旨在比较苯达莫司汀/泼尼松龙与标准美法仑/泼尼松龙方案的疗效。