Yamamoto Hisashi, Uchida Naoyuki, Yuasa Mitsuhiro, Kageyama Kosei, Ota Hikari, Kaji Daisuke, Nishida Aya, Ishiwata Kazuya, Takagi Shinsuke, Tsuji Masanori, Asano-Mori Yuki, Yamamoto Go, Izutsu Koji, Masuoka Kazuhiro, Wake Atsushi, Yoneyama Akiko, Makino Shigeyoshi, Taniguchi Shuichi
Department of Hematology, Toranomon Hospital, Tokyo, Japan.
Department of Hematology, Toranomon Hospital, Tokyo, Japan; Okinaka Memorial Institute for Medical Research, Tokyo, Japan.
Biol Blood Marrow Transplant. 2016 Oct;22(10):1844-1850. doi: 10.1016/j.bbmt.2016.06.017. Epub 2016 Jun 21.
A pilot study of a novel, reduced-toxicity, myeloablative conditioning regimen using intravenous busulfan 12.8 mg/kg, fludarabine 180 mg/m(2), and melphalan 80 mg/m(2) for single cord blood transplantation (CBT) was conducted at our institution. Fifty-one patients with myeloid malignancies not in remission were included in this study. Their median age was 59 years (range, 19 to 70 years), with a median hematopoietic cell transplantation-specific comorbidity index score of 3. With a median observation period of 39.6 months (range, 24.3 to 90.8 months) among the survivors, overall survival and progression-free survival at 2 years were both 54.9%. Forty-six of 51 achieved neutrophil engraftment at a median of 19.5 days (range, 13 to 38 days) after transplantation, with a cumulative incidence of 90.2%. No patient developed graft rejection in this study. All patients who achieved engraftment showed hematological complete remission with complete donor chimerism. Eleven patients relapsed at a median of 4.9 months (range, .5 to 26.7 months). Cumulative incidences of nonrelapse mortality (NRM) at 100 days and 2 years were 11.8% and 25.5%, respectively. In conclusion, the present results show that the novel conditioning regimen for single CBT provided durable engraftment and remission with acceptable NRM leading to excellent survival, even for a relatively older population with myeloid malignancies not in remission.
我们机构开展了一项初步研究,采用静脉注射白消安12.8mg/kg、氟达拉滨180mg/m²和马法兰80mg/m²的新型低毒性清髓性预处理方案进行单份脐血移植(CBT)。本研究纳入了51例未缓解的髓系恶性肿瘤患者。他们的中位年龄为59岁(范围19至70岁),造血细胞移植特异性合并症指数评分中位数为3。幸存者的中位观察期为39.6个月(范围24.3至90.8个月),2年总生存率和无进展生存率均为54.9%。51例患者中有46例在移植后中位19.5天(范围13至38天)实现中性粒细胞植入,累积发生率为90.2%。本研究中无患者发生移植物排斥反应。所有实现植入的患者均表现出血液学完全缓解且供者完全嵌合。11例患者复发,中位复发时间为4.9个月(范围0.5至26.7个月)。100天和2年时非复发死亡率(NRM)的累积发生率分别为11.8%和25.5%。总之,目前的结果表明,单份CBT的新型预处理方案可实现持久植入和缓解,NRM可接受,从而带来优异的生存率,即使对于相对年长的未缓解髓系恶性肿瘤患者也是如此。