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Rituximab: enhancing outcome of autologous stem cell transplantation in non-Hodgkin's lymphoma.

机译:利妥昔单抗:在非霍奇金淋巴瘤中增强自体干细胞移植的结果。

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摘要

High-dose chemotherapy and autologous stem cell transplantation (ASCT) is a potentially curative therapy for younger patients with relapsed aggressive non-Hodgkin's lymphoma, and is under investigation as first-line treatment and as therapy for indolent and mantle cell non-Hodgkin's lymphoma. However, between 40% and 70% of all patients relapse after ASCT because of contamination of the stem cell product or persistence of residual tumor cells. Evidence is emerging that the administration of rituximab as an in vivo purging agent before ASCT is effective in eliminating lymphoma cell contamination, as measured by clearance of bcl-2-positive cells from stem cell harvests. Furthermore, in vivo purging with rituximab does not adversely affect the stem cell yield or function. Maintenance therapy with rituximab post-transplantation has also been explored as a means of eliminating residual tumor cells. Results suggest that rituximab may eradicate minimal residual disease post-transplant and help prevent relapse. The efficacy of both in vivo purging and maintenance therapy with rituximab is currently being investigated in a large, multicenter, randomized trial by the European Group for Blood and Bone Marrow Transplantation in patients with follicular non-Hodgkin's lymphoma. Results from this and other ongoing trials will confirm the full potential of rituximab in ASCT.
机译:大剂量化疗和自体干细胞移植(ASCT)对于年轻的复发性侵袭性非霍奇金淋巴瘤患者是一种可能的治疗方法,目前正在作为一线治疗以及惰性和套细胞非霍奇金淋巴瘤的治疗方法进行研究。但是,由于干细胞产物的污染或残留肿瘤细胞的持续存在,所有患者中有40%至70%在ASCT后复发。越来越多的证据表明,如通过从干细胞收获物中清除bcl-2阳性细胞所测量的那样,在ASCT之前给予利妥昔单抗作为体内清除剂可有效消除淋巴瘤细胞污染。此外,用利妥昔单抗进行体内清除不会不利地影响干细胞的产量或功能。利妥昔单抗在移植后的维持治疗也已被研究作为消除残留肿瘤细胞的一种手段。结果表明,利妥昔单抗可以根除移植后的残留病,并有助于预防复发。欧洲血液和骨髓移植组织在滤泡性非霍奇金淋巴瘤患者中进行的一项大型,多中心,随机试验中,目前正在研究利妥昔单抗的体内清除和维持疗法的疗效。该试验和其他正在进行的试验的结果将证实利妥昔单抗在ASCT中的全部潜力。

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