Vela-Ojeda Jorge, Ruiz-Esparza Miriam A García
Hospital de Especialidades Centro Médico La Raza, IMSS.
Rev Invest Clin. 2005 Mar-Apr;57(2):305-13.
Multiple myeloma (MM) is the second most common hematologic malignancy, affecting approximately 14,000 new patients per year in the United States. For over four decades, the standard treatment for MM has been a regimen of melphalan combined with prednisone. Using this treatment modality, complete responses are rare, and 50% of patients have had disease that was resistant to chemotherapy. Attempts have been made to improve the outcome of MM by administering combinations of i.v. poli-chemotherapy, but these treatments are equivalent in terms of overall survival. High-dose therapy with peripheral blood stem cell support can be applied safely in these patients and achieves significantly higher complete remission rates as well as better event-free survival and overall survival. However, neither tumor-cell purging, positive selection, intensification of conditioning with additional chemotherapeutic agents, nor total body irradiation have been shown to improve outcome. The role of tandem transplantation with high-dose melphalan seems to be a good selection of treatment in hospitals having all resources. Future research will include the combination of the best remission-induction regimen with tandem transplants and maintenance treatments (thalidomide, idiotype or dendritic cell vaccination) that will sustain complete remission. Development of non-myeloablative allogeneic transplantation in order to exploit the graft-versus myeloma effect provides an alternative for patients who have a compatible donor. Combining all of these modalities with the new drugs developed few years ago (thalidomide, bortezomib, revlimid), we hope that MM will become a manageable chronic disease and perhaps a curable disease at least for 30% to 40% of the patients.
多发性骨髓瘤(MM)是第二常见的血液系统恶性肿瘤,在美国每年约有14000名新发病例。四十多年来,MM的标准治疗方案一直是美法仑联合泼尼松。采用这种治疗方式,完全缓解很少见,50%的患者对化疗耐药。人们尝试通过静脉联合化疗来改善MM的治疗效果,但这些治疗在总生存期方面并无差异。外周血干细胞支持下的大剂量治疗可安全应用于这些患者,并能显著提高完全缓解率,以及改善无事件生存期和总生存期。然而,肿瘤细胞清除、阳性选择、增加化疗药物强化预处理以及全身照射均未显示能改善治疗效果。在具备所有资源的医院中,大剂量美法仑序贯移植似乎是一种不错的治疗选择。未来的研究将包括最佳缓解诱导方案与序贯移植及维持治疗(沙利度胺、独特型或树突状细胞疫苗接种)的联合,以维持完全缓解。开发非清髓性异基因移植以利用移植物抗骨髓瘤效应,为有合适供者的患者提供了一种选择。将所有这些治疗方式与几年前研发的新药(沙利度胺、硼替佐米、来那度胺)相结合,我们希望MM将成为一种可控制的慢性病,甚至可能至少使30%至40%的患者得以治愈。