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通过长期骨髓培养评估自体骨髓移植患者的造血功能。

Haemopoiesis of transplanted patients with autologous marrows assessed by long-term marrow culture.

作者信息

Domenech J, Gihana E, Dayan A, Truglio D, Linassier C, Desbois I, Lamagnere J P, Colombat P, Binet C

机构信息

Department of Medical Oncology and Blood Diseases, University Hospital of Tours, France.

出版信息

Br J Haematol. 1994 Nov;88(3):488-96. doi: 10.1111/j.1365-2141.1994.tb05064.x.

Abstract

We assessed the effect of antitumoural therapy at intensive doses on the haemopoietic system using long-term marrow cultures (LTMC) established from 33 patients (25 with haematological diseases and eight with solid tumours) after autologous bone marrow transplantation (ABMT). When compared to 42 pre-graft patients, a decreased CFU-GM production and a defect in stromal layer (SL) confluence were found after ABMT on day 90 but also on day 365. However, these abnormalities were observed only in patients with haematological diseases and no differences between pre-graft and post-graft results were found in patients with solid tumours. Among the patients with haematological diseases, on day 90 those with acute lymphoid leukaemias showed lower CFU-GM production whereas patients with non-Hodgkin's lymphomas developed more frequently subconfluent or confluent SL. Other factors studied such as sex, patient age, disease status, marrow purging and post-graft administration of growth factors did not appear to influence post-graft LTMC results. Multivariate analysis including all the patients has shown (a) that solid tumours were associated with higher CFU-GM production, and (b) that conditioning regimens with total body irradiation (TBI) or busulfan led more frequently to non-confluent SL. In conclusion, high-dose therapy followed by ABMT can induce a persistent impairment of the stem cell and stromal cell compartments, particularly in patients with haematological diseases conditioned with TBI, despite the absence of any alloimmune reaction and post-graft immunosuppressive therapy.

摘要

我们采用从33例患者(25例血液系统疾病患者和8例实体瘤患者)自体骨髓移植(ABMT)后建立的长期骨髓培养(LTMC),评估了大剂量抗肿瘤治疗对造血系统的影响。与42例移植前患者相比,在ABMT后第90天以及第365天,发现CFU-GM生成减少且基质层(SL)汇合存在缺陷。然而,这些异常仅在血液系统疾病患者中观察到,实体瘤患者移植前和移植后的结果未发现差异。在血液系统疾病患者中,第90天时,急性淋巴细胞白血病患者的CFU-GM生成较低,而非霍奇金淋巴瘤患者的SL更常出现亚汇合或汇合状态。所研究的其他因素,如性别、患者年龄、疾病状态、骨髓净化以及移植后生长因子的使用,似乎并未影响移植后LTMC的结果。对所有患者进行的多因素分析显示:(a)实体瘤与较高的CFU-GM生成相关;(b)采用全身照射(TBI)或白消安的预处理方案更常导致SL不汇合。总之,尽管没有任何同种免疫反应和移植后免疫抑制治疗,但大剂量治疗后进行ABMT可导致干细胞和基质细胞区室持续受损,尤其是接受TBI预处理的血液系统疾病患者。

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