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Should eligible patients with T-cell lymphoma receive high-dose therapy and autologous stem cell transplant in the upfront setting?

机译:合格的T细胞淋巴瘤患者是否应在大环境中接受大剂量治疗和自体干细胞移植?

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摘要

Peripheral T-cell lymphomas (PTCL) are rare and aggressive subtypes of non-Hodgkin's lymphoma. Compared to B cell lymphomas, the immunologic phenotype of PTCL portends a poorer prognosis, with the exception of anaplastic large cell lymphoma bearing the anaplastic lymphoma kinase protein. Patients with PTCL tend to present clinically in advanced disease states, show lower response rates to chemotherapy, and suffer from more frequent relapses and shorter remissions. The rarity of these lymphomas has made it difficult to carry out prospective, randomized trials delineating optimal treatments. Conventional and intensified chemotherapy have led to reasonable responses, but in many studies, frequent relapses. Consequently, high-dose chemotherapy and autologous stem cell transplantation (ASCT) have been actively studied in both the relapsed and upfront setting. In addition, the impact of disease status at transplantation is being investigated, though the optimal disease state at transplant is still a matter of debate, as is the timing of transplant. This article seeks to review the literature on the role of ASCT in PTCL, as well as to clarify what may be the optimal disease state in which to offer patients with PTCL autologous transplantation, if at all.
机译:外周T细胞淋巴瘤(PTCL)是非霍奇金淋巴瘤的罕见和侵袭性亚型。与B细胞淋巴瘤相比,PTCL的免疫表型预后较差,除了带有间变性淋巴瘤激酶蛋白的间变性大细胞淋巴瘤外。 PTCL患者往往在临床上处于晚期疾病状态,对化疗的反应率较低,并且复发频率更高且缓解时间更短。这些淋巴瘤的罕见性使得难以开展描述最佳治疗方法的前瞻性随机试验。常规和强化化疗已导致合理的反应,但在许多研究中,复发频繁。因此,已经在复发和前期环境中积极研究了大剂量化学疗法和自体干细胞移植(ASCT)。另外,尽管移植时的最佳疾病状态以及移植时机仍在争论中,但仍在研究移植时疾病状态的影响。本文旨在回顾有关ASCT在PTCL中的作用的文献,并弄清为PTCL自体移植患者提供的最佳疾病状态(如果有的话)。

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