Tricot G, Jagannath S, Vesole D H, Bracy D, Desikan K R, Siegel D, Barlogie B
Division of Hematology/Oncology, University of Arkansas for Medical Sciences, Little Rock, USA.
Leuk Lymphoma. 1996 Jun;22(1-2):25-36. doi: 10.3109/10428199609051725.
Standard chemotherapy with melphalan-prednisone or a combination of alkylating agents has not extended the overall survival of patients with multiple myeloma during the last 30 years and strictly defined complete remissions (CR) are exceedingly rare. The early mortality with conventional therapy varies between 2 and 10 percent. A substantial increase in the dose of melphalan (100-140 mg/m2) has resulted in a 30-45% CR rate in newly diagnosed patients and an overall survival advantage of approximately 1 year. However, treatment related morbidity and mortality, due to prolonged cytopenia was unacceptably high. Based on these findings the dose intensity was further increased by either escalating melphalan to 200 mg/m2 or by adding total body irradiation, while at the same time providing stem cell support to shorten the duration of cytopenia. Autologous transplants, especially with peripheral blood stem cells and hematopoietic growth factors, can now be performed safely up to the age of 70 with a low transplant-related mortality (2-10%). A CR is attained in approximately 50% of previously untreated patients and 10-20% of refractory cases. Overall survival of newly diagnosed and refractory patients treated with autotransplants appears superior to that of patients receiving conventional chemotherapy. Therefore, autotransplantation should be considered as a treatment option in all patients with multiple myeloma at least up to the age of 65. Despite these encouraging findings, most myeloma patients ultimately relapse and the survival curves do not suggest that autotransplantation as currently performed is a curative approach in a substantial proportion of patients. Further improvement with autotransplants should be achieved by providing tumor-free grafts and by introducing post-transplantation manipulations, aimed at eradicating minimal residual disease.
在过去30年中,使用美法仑-泼尼松进行的标准化疗或烷化剂联合化疗并未延长多发性骨髓瘤患者的总生存期,严格定义的完全缓解(CR)极为罕见。传统疗法的早期死亡率在2%至10%之间。美法仑剂量大幅增加(100 - 140 mg/m²)使新诊断患者的CR率达到30% - 45%,总生存期优势约为1年。然而,由于长期血细胞减少导致的治疗相关发病率和死亡率高得令人难以接受。基于这些发现,通过将美法仑剂量增至200 mg/m²或添加全身照射进一步提高剂量强度,同时提供干细胞支持以缩短血细胞减少的持续时间。自体移植,尤其是外周血干细胞和造血生长因子的自体移植,现在在70岁以下患者中可以安全进行,移植相关死亡率较低(2% - 10%)。约50%的既往未治疗患者和10% - 20%的难治性病例可实现CR。接受自体移植治疗的新诊断和难治性患者的总生存期似乎优于接受传统化疗的患者。因此,对于所有多发性骨髓瘤患者,至少在65岁以下,应考虑将自体移植作为一种治疗选择。尽管有这些令人鼓舞的发现,但大多数骨髓瘤患者最终会复发,生存曲线并不表明目前进行的自体移植在很大比例的患者中是一种治愈方法。应通过提供无肿瘤移植物和引入旨在根除微小残留病的移植后操作来进一步改善自体移植效果。