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首页> 外文期刊>Journal of Cancer Research and Clinical Oncology >Allogeneic hematopoietic cell transplantation: from experimental biology to clinical care.
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Allogeneic hematopoietic cell transplantation: from experimental biology to clinical care.

机译:异基因造血细胞移植:从实验生物学到临床护理。

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摘要

PURPOSE: For more than half a century, researchers have explored myeloablative, high-dose chemo/radiotherapy followed by allogeneic hematopoietic stem cell transplantation (HCT) for therapy of malignant and nonmalignant hematological diseases. Continuous advances in the field have changed this approach from one that was initially thought to be fraught by insurmountable complications to one that is now considered standard therapy for many diseases. METHODS: In order to extend allogeneic HCT to include elderly patients, who represent the main population affected by hematological malignancies, and to those who are medically unfit to undergo conventional HCT, novel non-myeloablative approaches have been developed. These approaches rely on graft-vs-tumor effects for tumor eradication rather than high-dose chemoradiotherapy, and, accordingly, have lower toxicities than conventional regimens. RESULTS: Results with non-myeloablative regimens have been gratifying, and this may change the future of allogeneic HCT. Advances could not have been possible without basic research and studies in pre-clinical animal models. CONCLUSION: Further work is focused on improving graft-vs-tumor effects while achieving better control of graft-vs-host disease.
机译:目的:半个多世纪以来,研究人员探索了清髓性,大剂量化学/放射疗法,然后进行异基因造血干细胞移植(HCT),用于治疗恶性和非恶性血液病。该领域的不断进步已将这种方法从最初被认为难以克服的并发症所困扰的方法转变为如今被认为是许多疾病的标准疗法的方法。方法:为了将同种异体HCT扩大到包括受血液系统恶性肿瘤影响的主要人群的老年患者,以及在医学上不适合常规HCT的患者,已开发出新颖的非清髓性方法。这些方法依靠移植物抗肿瘤效应来根除肿瘤,而不是大剂量放化疗,因此毒性比常规方案低。结果:非清髓疗法的结果令人欣喜,这可能改变同种异体HCT的未来。没有基础临床研究和临床前动物模型的研究就不可能取得进展。结论:进一步的工作侧重于改善移植物抗肿瘤的效果,同时更好地控制移植物抗宿主病。

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