Valente Maria, Roy Vivek, Lacy Martha Q, Dispenzieri Angela, Gertz Morie A
Mayo Clinic, Jacksonville, Florida, USA.
Leuk Lymphoma. 2006 Jun;47(6):1006-12. doi: 10.1080/10428190600572624.
High dose chemotherapy (HDC) followed by autologous stem cell transplant (ASCT) is an accepted form of treatment for patients with AL amyloidosis. The purpose of the current study is to review the outcomes of IgM AL amyloidosis patients treated with high dose chemotherapy and autologous stem cell transplant and compare them to the outcomes of all AL amyloidosis subtypes treated similarly. We retrospectively reviewed the pretransplant characteristics, conditioning regimens and response to transplant of all twelve IgM AL amyloidosis patients who were transplanted at the Mayo Clinic between May 1999 and August 2005. Transplant related mortality was low at 8%. The overall hematologic response rate was 89%. The organ response rate was 67%. Overall median survival has not been reached as eleven patients are still alive. IgM AL amyloidosis patients appear to have similar outcomes after HDC and ASCT as other subtypes of AL amyloidosis suggesting that this therapy is an acceptable form of treatment for patients with IgM amyloidosis, and should be considered as a first line treatment option.
大剂量化疗(HDC)后进行自体干细胞移植(ASCT)是治疗 AL 淀粉样变性患者的一种公认治疗方式。本研究的目的是回顾接受大剂量化疗和自体干细胞移植治疗的 IgM 型 AL 淀粉样变性患者的治疗结果,并将其与接受类似治疗的所有 AL 淀粉样变性亚型的结果进行比较。我们回顾性分析了 1999 年 5 月至 2005 年 8 月间在梅奥诊所接受移植的 12 例 IgM 型 AL 淀粉样变性患者的移植前特征、预处理方案及移植反应。移植相关死亡率较低,为 8%。总体血液学缓解率为 89%。器官缓解率为 67%。由于 11 名患者仍存活,总体中位生存期尚未达到。IgM 型 AL 淀粉样变性患者在接受大剂量化疗和自体干细胞移植后的结果似乎与其他 AL 淀粉样变性亚型相似,这表明该疗法是 IgM 淀粉样变性患者可接受的治疗方式,应被视为一线治疗选择。