Tura S, Cavo M
University of Bologna, Italy.
Hematol Oncol Clin North Am. 1992 Apr;6(2):425-35.
The use of high-dose chemoradiotherapy with allogeneic hemopoietic stem cell support for the treatment of MM began about a decade ago. Because this procedure has been performed increasingly and because larger numbers of patients are being followed for longer periods of time, the proper role of allogeneic BMT in this setting is becoming clearer. Data available thus far indicate that such an approach results in a complete remission rate of at least 50% to 60%, and even higher if applied as consolidation treatment in the remission phase, a transplant-related mortality reported as 40% to 50% and a long-term survival plateau at around 40%. The 40% 5-year probability of relapse-free survival is considerably higher than that observed following autologous BMT and may result from an allogeneic graft-versus-tumor effect (graft versus myeloma) similar to the well-recognized graft-versus-leukemia effect. Although follow-up is still too short to clearly identify the likelihood of cure for MM allotransplant recipients, a certain number of them are currently long-term, disease-free survivors and--we hope--cured. These promising results and the incurability of MM with conventional chemotherapy should, therefore, encourage further application of allogeneic BMT to selected patients with unfavorable prognostic features. Continued efforts to reduce the morbidity and mortality related to the procedure, as well as to design effective pretransplant regimens with lower extramedullary toxicity and to identify those patients most likely to benefit from BMT, will improve the value of allogeneic BMT in MM.
大约十年前开始使用大剂量放化疗联合异基因造血干细胞支持来治疗多发性骨髓瘤(MM)。由于这种治疗方法的应用越来越多,并且有更多患者接受了更长时间的随访,异基因骨髓移植(BMT)在这种情况下的恰当作用正变得越来越清晰。目前可得的数据表明,这样一种治疗方法能使完全缓解率达到至少50%至60%,如果在缓解期作为巩固治疗应用,缓解率甚至更高,移植相关死亡率报告为40%至50%,长期生存率稳定在40%左右。40%的5年无复发生存概率显著高于自体BMT后的观察结果,这可能源于一种类似于广为人知的移植物抗白血病效应的异基因移植物抗肿瘤效应(移植物抗骨髓瘤)。尽管随访时间仍然太短,无法明确确定MM异基因移植受者的治愈可能性,但目前有一定数量的患者是长期无病生存者,而且我们希望他们已被治愈。因此,这些有前景的结果以及MM用传统化疗无法治愈的情况,应该会鼓励对有不良预后特征的特定患者进一步应用异基因BMT。持续努力降低与该治疗方法相关的发病率和死亡率,以及设计具有更低髓外毒性的有效移植前方案,并确定那些最有可能从BMT中获益的患者,将提高异基因BMT在MM治疗中的价值。