Leoni F, Ciolli S, Salti F, Teodori P, Ferrini P R
Department of Haematology, University of Florence, Firenze, Italy.
Br J Haematol. 1991 Feb;77(2):180-4. doi: 10.1111/j.1365-2141.1991.tb07974.x.
Twenty-one patients with advanced refractory myeloma (nine primary unresponsive to melphalan, 12 relapsed and resistant to first-line salvage therapy) received monthly 7 d courses of cyclophosphamide by continuous infusion, associated with teniposide and dexamethasone. Six patients died within 2 months from start of treatment, before receiving an adequate trial. Among the 15 evaluable patients, there were eight objective responses and three improvements (decrease of monoclonal protein greater than 50% or greater than 30%, respectively). After a median follow-up of 10 months, all responding patients are alive and none of them is still relapsed. In heavily pretreated patients, ineligible for more aggressive approaches, cyclophosphamide by continuous-infusion exerted a good antineoplastic activity without increasing toxicity.
21例晚期难治性骨髓瘤患者(9例对美法仑原发性无反应,12例复发且对一线挽救治疗耐药)接受每月7天的环磷酰胺持续静脉输注疗程,并联合替尼泊苷和地塞米松。6例患者在开始治疗后2个月内死亡,未接受充分的试验。在15例可评估患者中,有8例客观缓解,3例病情改善(单克隆蛋白分别降低大于50%或大于30%)。中位随访10个月后,所有缓解患者均存活,且无一例复发。在接受过大量预处理、不适合采用更积极治疗方法的患者中,持续静脉输注环磷酰胺显示出良好的抗肿瘤活性,且未增加毒性。