Link H, Kolb H J, Ebell W, Hossfeld D K, Zander A, Niethammer D, Wandt H, Grosse-Wilde H, Schaefer U W
Abteilung Hämatologie und Onkologie, Zentrum Innere Medizin, Medizinische Hochschule Hannover.
Med Klin (Munich). 1997 Sep 15;92(9):534-45. doi: 10.1007/BF03044929.
The destruction of hematopoiesis and lymphopoiesis by total body irradiation or high dose chemotherapy for the treatment of malignancy can be reversed by the transplantation of allogeneic or autologous hematopoietic stem cells. In primary disorders of bone marrow or immune system, allogeneic stem cells replace deficient cells. Acute leukemias can be cured, with in 50 to 80% disease free survival after 5 to 8 years. The allogeneic graft versus leukemia effect by immunoreactive cells reduces the relapse rate in myeloid and lymphoid malignancies. 40 to 70% of patients with chronic myeloid leukemia remain disease free after more than 5 years. Patients with malignant lymphoma have a 40 to 70% chance of cure with autologous transplantation, which is not increased by allogeneic cells, because of a higher incidence of severe complications. An increasing number of patients without option for cure is treated with the aim of prolonging remission or retarding disease progression, such as in chronic myeloid leukemia, multiple myeloma and certain solid tumors. New studies suggest in breast cancer with axillary lymph node metastases, that adjuvant high dose chemotherapy with autologous stem cell support will significantly improve disease free survival from 30 to over 60% after 3 to 5 years. In congenital metabolic and storage diseases deficient enzymes are substituted by the allogeneic cells. Clinical trials explore the use of stem cell transplantation after myeloablative therapy in autoimmune disorders as well as in gene therapy with transfected hematopoietic stem cells.
通过全身照射或高剂量化疗治疗恶性肿瘤时,造血和淋巴细胞生成的破坏可通过同种异体或自体造血干细胞移植来逆转。在骨髓或免疫系统的原发性疾病中,同种异体干细胞可替代缺陷细胞。急性白血病可以治愈,5至8年后无病生存率可达50%至80%。免疫反应性细胞产生的同种异体移植物抗白血病效应可降低髓系和淋巴系恶性肿瘤的复发率。40%至70%的慢性髓性白血病患者5年以上无病生存。恶性淋巴瘤患者自体移植治愈的几率为40%至70%,由于严重并发症发生率较高,同种异体细胞移植并未提高治愈率。越来越多无法治愈的患者接受治疗,目的是延长缓解期或延缓疾病进展,如慢性髓性白血病、多发性骨髓瘤和某些实体瘤。新的研究表明,在有腋窝淋巴结转移的乳腺癌中,辅助性高剂量化疗加自体干细胞支持将使3至5年后的无病生存率从30%显著提高到60%以上。在先天性代谢和储存疾病中,缺陷酶由同种异体细胞替代。临床试验探索了在自身免疫性疾病中清髓性治疗后使用干细胞移植以及使用转染造血干细胞进行基因治疗的情况。