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[恶性血液病中骨髓和外周血干细胞移植的适应证]

[Indications for bone marrow and peripheral stem cell transplantation in malignant hematological diseases].

作者信息

Gratwohl A

机构信息

Abteilung für Hämatologie, Departement Innere Medizin, Kantonsspital Basel.

出版信息

Ther Umsch. 1996 Feb;53(2):152-7.

PMID:8629266
Abstract

Transplantation of hematopoietic precursor cells is an established therapy today in the treatment of hematological malignancies. Cells from different sources [bone marrow, peripheral blood, cord blood] and from different donor types [autologous, syngeneic or allogeneic] are used for transplantation. The aim of autologous transplantation is to apply intensive high-dose chemo-radiotherapy and to shorten the duration of aplasia. Allogeneic cells, in addition, are free of potentially contaminating precursor cells and provide a graft-versus-leukemia effect. For all patients, transplantation should be considered at diagnosis as an integral part of treatment strategy and, depending on risk factors, be performed early in the course of disease. Preferred time for patients with high-risk acute leukemias is first complete remission, second complete remission for standard or low-risk acute leukemias. For chronic myeloid leukemia, allogeneic transplantation should be performed within one year of diagnosis, preferably still in first chronic phase. Autologous transplantation can be considered in a protocol setting. For patients with myelodysplastic syndromes of the FAB subtype refractory anemia or refractory anemia with sideroblasts, allogeneic transplantation is the treatment of choice as initial therapy. For patients with refractory anemia and excess of blasts with or without transformation, remission induction should be attempted before transplantation. Autologous transplantation is the preferred treatment strategy for patients with Hodgkin's and non-Hodgkin's lymphoma, for high-risk patients in first complete remission, for other patients in chemotherapy-sensitive first relapse. For patients with myeloma, transplantation should be considered after first line therapy. Age is the main individual patient's risk factor, transplant-related mortality immediately increases in parallel to increasing age. Autologous transplants are limited to patients below 60 to 65 years, allogeneic HLA-identical sibling transplants to patients below 50 to 55 years, and unrelated transplants to patients below 40 to 45 years. Prerequisites for transplant are availability of a donor, access to a transplant bed, informed consent of patient and donor, as well as financial guarantee. Indications for the different hematological malignancies and the major risk factors are discussed.

摘要

造血前体细胞移植是目前治疗血液系统恶性肿瘤的一种成熟疗法。来自不同来源(骨髓、外周血、脐带血)和不同供体类型(自体、同基因或异基因)的细胞用于移植。自体移植的目的是进行强化大剂量放化疗,并缩短再生障碍期的持续时间。此外,异基因细胞不含潜在污染的前体细胞,并具有移植物抗白血病效应。对于所有患者,移植应在诊断时作为治疗策略的一个组成部分加以考虑,并根据危险因素,在病程早期进行。高危急性白血病患者的首选时机是首次完全缓解期,标准或低危急性白血病患者是第二次完全缓解期。对于慢性髓性白血病,异基因移植应在诊断后一年内进行,最好仍处于第一慢性期。自体移植可在方案设定中予以考虑。对于FAB亚型难治性贫血或伴有环形铁粒幼细胞的难治性贫血的骨髓增生异常综合征患者,异基因移植是作为初始治疗的首选。对于伴有或不伴有转化的难治性贫血伴原始细胞增多患者,在移植前应尝试诱导缓解。自体移植是霍奇金淋巴瘤和非霍奇金淋巴瘤患者、首次完全缓解期的高危患者、化疗敏感的首次复发的其他患者的首选治疗策略。对于骨髓瘤患者,应在一线治疗后考虑移植。年龄是主要的个体患者危险因素,移植相关死亡率随年龄增长而立即上升。自体移植限于60至65岁以下的患者,同基因HLA匹配的同胞移植限于50至55岁以下的患者,非血缘移植限于40至45岁以下的患者。移植的前提条件是有供体、有移植床位、患者和供体的知情同意以及资金保障。讨论了不同血液系统恶性肿瘤的适应证和主要危险因素。

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