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骨髓瘤或淀粉样变性且严重肾功能损害患者接受大剂量化疗和自体干细胞移植的临床结局及毒性:一项英国血液与骨髓移植学会的研究

The clinical outcome and toxicity of high-dose chemotherapy and autologous stem cell transplantation in patients with myeloma or amyloid and severe renal impairment: a British Society of Blood and Marrow Transplantation study.

作者信息

Bird Jennifer M, Fuge Rhian, Sirohi Bhawna, Apperley Jane F, Hunter Ann, Snowden John, Mahendra Premini, Milligan Donald, Byrne Jenny, Littlewood Timothy, Fegan Christopher, McQuaker Grant, Pagliuca Antonio, Johnson Peter, Rahemtulla Amin, Morris Curly, Marks David I

机构信息

Bristol Haematology and Oncology Centre, Bristol, UK.

出版信息

Br J Haematol. 2006 Aug;134(4):385-90. doi: 10.1111/j.1365-2141.2006.06191.x. Epub 2006 Jul 5.

Abstract

The outcome of high-dose chemotherapy (HDT) was evaluated retrospectively in 27 patients with myeloma and four patients with AL amyloidosis with severe renal impairment. Twenty-three patients were receiving dialysis and the rest had a creatinine clearance of <20 ml/min. The median melphalan dose was 140 mg/m2 (range: 60-200 mg/m2), but 10 patients (37%) received 200 mg/m2. Myeloid and platelet engraftment were similar to that seen in patients without renal failure. Five of 27 patients died of transplant-related toxicity before the day 100. Twenty of 27 patients had a response (70%). The median time to disease progression was 32 months (range: 6-54 months) and the median time to best response was 6.5 months. Four of 17 evaluable patients (24%) became dialysis-independent at a median of 5 months post-HDT/stem cell transplantation. At a median follow-up of 70 months, 7/23 patients with myeloma were alive but three of these seven patients had progressive disease. Two of the four patients with amyloidosis have survived. HDT is feasible in these patients and results in 5-year survival in about one-third of patients.

摘要

对27例骨髓瘤患者和4例伴有严重肾功能损害的AL淀粉样变性患者进行了大剂量化疗(HDT)疗效的回顾性评估。23例患者正在接受透析,其余患者的肌酐清除率<20 ml/min。美法仑的中位剂量为140 mg/m²(范围:60 - 200 mg/m²),但10例患者(37%)接受了200 mg/m²的剂量。髓系和血小板植入情况与无肾衰竭患者相似。27例患者中有5例在第100天前死于移植相关毒性。27例患者中有20例有反应(70%)。疾病进展的中位时间为32个月(范围:6 - 54个月),最佳反应的中位时间为6.5个月。17例可评估患者中有4例(24%)在HDT/干细胞移植后中位5个月时不再依赖透析。中位随访70个月时,23例骨髓瘤患者中有7例存活,但这7例患者中有3例疾病进展。4例淀粉样变性患者中有2例存活。HDT在这些患者中是可行的,约三分之一的患者可实现5年生存。

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