Harousseau J L, Attal M, Divine M, Marit G, Leblond V, Stoppa A M, Bourhis J H, Caillot D, Boasson M, Abgrall J F
Department of Hematology, Hôtel-Dieu, Nantes, France.
Stem Cells. 1995 Aug;13 Suppl 2:132-9. doi: 10.1002/stem.5530130721.
Eighteen French centers reported 133 autologous stem cell transplantations performed after first remission induction in multiple myeloma. The source of stem cell was marrow (81 cases), blood (51 cases) or marrow plus blood (1 case). The immediate outcome after transplantation was 49 (37%) complete remissions (CR; 13 maintained, 36 achieved), 61 (46%) partial remissions, 17 failures and 5 toxic deaths. With a median follow up of 35 months, the median remission duration was 33 months, the median time to treatment failure was 22 months. The median overall survival was 46 months, 54 months for the 103 patients responding to primary treatment and 30 months for the 30 nonresponders. In univariate analysis, the outcome was influenced by age, Ig isotype, initial beta 2-Microglobulin level, response to initial chemotherapy, plasma cell marrow involvement at the time of harvest, albumin and beta 2-Microglobulin level at the time of transplantation and CR achievement after transplantation. In multivariate analysis, the most important prognostic factor was the quality of response after transplantation. The conditioning regimen and the source of stem cell had no significant impact on immediate and long-term results. Maintenance therapy with alpha interferon did not appear to prolong remission duration or survival. Autologous stem cell transplantation is an effective consolidation for patients responding to primary treatment and a salvage therapy for some nonresponding patients. This approach has to be compared to conventional chemotherapy in prospective randomized studies. The critical impact of CR achievement on survival implies new strategies in order to increase the CR rate.
18个法国中心报告了133例多发性骨髓瘤首次缓解诱导后进行的自体干细胞移植。干细胞来源为骨髓(81例)、血液(51例)或骨髓加血液(1例)。移植后的近期结果为49例(37%)完全缓解(CR;13例维持,36例达到),61例(46%)部分缓解,17例失败,5例因毒性死亡。中位随访35个月,中位缓解持续时间为33个月,中位治疗失败时间为22个月。中位总生存期为46个月,103例对初始治疗有反应的患者为54个月,30例无反应者为30个月。单因素分析中,结果受年龄、免疫球蛋白亚型、初始β2-微球蛋白水平、对初始化疗的反应、采集时浆细胞骨髓受累情况、移植时白蛋白和β2-微球蛋白水平以及移植后CR的实现情况影响。多因素分析中,最重要的预后因素是移植后反应的质量。预处理方案和干细胞来源对近期和长期结果无显著影响。α干扰素维持治疗似乎并未延长缓解持续时间或生存期。自体干细胞移植对初始治疗有反应的患者是一种有效的巩固治疗,对一些无反应患者是一种挽救治疗。这种方法必须在前瞻性随机研究中与传统化疗进行比较。CR的实现对生存的关键影响意味着需要新的策略来提高CR率。