Dana Farber Cancer Institute, Boston, Massachusetts 02115, USA.
Biol Blood Marrow Transplant. 2010 Aug;16(8):1037-69. doi: 10.1016/j.bbmt.2010.05.005. Epub 2010 May 24.
Prevention of relapse after allogeneic hematopoietic stem cell transplantation is the most likely approach to improve survival of patients treated for hematologic malignancies. Herein we review the limits of currently available transplant therapies and the innovative strategies being developed to overcome resistance to therapy or to fill therapeutic modalities not currently available. These novel strategies include nonimmunologic therapies, such as targeted preparative regimens and posttransplant drug therapy, as well as immunologic interventions, including graft engineering, donor lymphocyte infusions, T cell engineering, vaccination, and dendritic cell-based approaches. Several aspects of the biology of the malignant cells as well as the host have been identified that obviate success of even these newer strategies. To maximize the potential for success, we recommend pursuing research to develop additional targeted therapies to be used in the preparative regimen or as maintenance posttransplant, better characterize the T cell and dendritic cells subsets involved in graft-versus-host disease and the graft-versus-leukemia/tumor effect, identify strategies for timing immunologic or nonimmunologic therapies to eliminate the noncycling cancer stem cell, identify more targets for immunotherapies, develop new vaccines that will not be limited by HLA, and develop methods to identify populations at very high risk for relapse to accelerate clinical development and avoid toxicity in patients not at risk for relapse.
异基因造血干细胞移植后预防复发是改善血液系统恶性肿瘤患者生存的最有可能的方法。在此,我们回顾了目前可用的移植治疗方法的局限性,以及正在开发的克服治疗耐药性或填补目前尚无治疗方法的创新策略。这些新策略包括非免疫治疗,如靶向预处理方案和移植后药物治疗,以及免疫干预,包括移植物工程、供者淋巴细胞输注、T 细胞工程、疫苗接种和树突状细胞方法。已经确定了恶性细胞和宿主的几个生物学方面,这些方面排除了即使是这些更新策略的成功。为了最大限度地提高成功的可能性,我们建议进行研究,开发额外的靶向治疗方法,用于预处理方案或移植后维持治疗,更好地描述移植物抗宿主病和移植物抗白血病/肿瘤效应中涉及的 T 细胞和树突状细胞亚群,确定免疫或非免疫治疗的时机策略,以消除非周期性癌症干细胞,确定更多的免疫治疗靶点,开发不受 HLA 限制的新疫苗,并开发识别高复发风险人群的方法,以加速临床开发并避免无复发风险患者的毒性。