Sanchorawala Vaishali, Brauneis Dina, Shelton Anthony C, Lo Stephen, Sun Fangui, Sloan J Mark, Quillen Karen, Seldin David C
Amyloidosis Center, Boston University School of Medicine and Boston Medical Center, Boston, Massachusetts.
Amyloidosis Center, Boston University School of Medicine and Boston Medical Center, Boston, Massachusetts.
Biol Blood Marrow Transplant. 2015 Aug;21(8):1445-51. doi: 10.1016/j.bbmt.2015.04.001. Epub 2015 Apr 6.
The depth of hematologic response has been shown to correlate with survival and organ responses for patients with light chain (AL) amyloidosis. We conducted a prospective trial of 2 cycles of induction with bortezomib and dexamethasone on a twice a week schedule followed by conditioning with bortezomib and high-dose melphalan (HDM) and autologous stem cell transplantation (SCT). The objectives were hematologic responses, tolerability, and survival. Thirty-five patients were enrolled from 2010 to 2013. Of these, 30 proceeded with SCT, whereas 5 did not because of clinical deterioration during induction (n = 3) or complications after stem cell collection (n = 2). Two patients developed features of an autologous graft-versus-host disease-like syndrome post-SCT, which responded to steroids; no other unusual complications were seen. Treatment-related mortality occurred in 8.5% (3/35). Hematologic responses were achieved by 100% of the 27 assessable patients (63% complete response, 37% very good partial response [VGPR]) who completed the planned treatment. By intention-to-treat, hematologic responses occurred in 77% of patients (49% complete response, 29% VGPR). With a median follow-up of 36 months, the median overall survival and progression-free survival were not reached. In conclusion, incorporating bortezomib into induction and conditioning yielded a high rate of hematologic responses after HDM/SCT in patients with AL amyloidosis.
对于轻链(AL)淀粉样变性患者,血液学缓解深度已被证明与生存率和器官反应相关。我们进行了一项前瞻性试验,采用硼替佐米和地塞米松每周两次进行2个周期的诱导治疗,随后用硼替佐米和大剂量美法仑(HDM)进行预处理并进行自体干细胞移植(SCT)。目的是观察血液学反应、耐受性和生存率。2010年至2013年共纳入35例患者。其中,30例进行了SCT,5例未进行,原因是诱导治疗期间临床病情恶化(3例)或干细胞采集后出现并发症(2例)。2例患者在SCT后出现了自体移植物抗宿主病样综合征的特征,对类固醇治疗有反应;未观察到其他异常并发症。治疗相关死亡率为8.5%(3/35)。完成计划治疗的27例可评估患者中100%获得了血液学反应(63%完全缓解,37%非常好的部分缓解[VGPR])。按意向性治疗分析,77%的患者出现血液学反应(49%完全缓解,29% VGPR)。中位随访36个月,中位总生存期和无进展生存期均未达到。总之,在AL淀粉样变性患者中,将硼替佐米纳入诱导和预处理方案后,HDM/SCT后的血液学反应率很高。