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起源细胞未能预测接受自体造血干细胞移植治疗的弥漫性大 B 细胞淋巴瘤患者的生存情况。

Cell of origin fails to predict survival in patients with diffuse large B-cell lymphoma treated with autologous hematopoietic stem cell transplantation.

机构信息

Department of Pathology and Microbiology, University of Nebraska Medical Center, Omaha, NE 68198-3135, USA.

出版信息

Hematol Oncol. 2012 Sep;30(3):143-9. doi: 10.1002/hon.1017. Epub 2011 Oct 18.

Abstract

Diffuse large B-cell lymphoma (DLBCL) includes two prognostically important subtypes, the germinal center B-cell (GCB) and the non-GCB types. The aim of this study was to evaluate immunohistochemical approaches for predicting the survival of patients with DLBCL following autologous hematopoietic stem cell transplantation (AHSCT). We identified 62 patients with DLBCL who either had an initial complete remission (17 patients) or received salvage chemotherapy for relapsed or refractory disease (45 patients), followed by AHSCT. Tissue microarrays were immunostained with monoclonal antibodies against GCET1, CD10, BCL6, MUM1, FOXP1 and LMO2. Using the Hans algorithm, we classified 50% of the cases as GCB type, whereas the Choi algorithm classified 58% as GCB type and LMO2 was positive in 69%. However, no significant differences were found in the 5-year overall or event-free survivals using any of these approaches. In conclusion, cell of origin fails to predict survival of DLBCL patients treated with AHSCT.

摘要

弥漫性大 B 细胞淋巴瘤(DLBCL)包括两种具有重要预后意义的亚型,即生发中心 B 细胞(GCB)和非 GCB 型。本研究旨在评估免疫组织化学方法预测接受自体造血干细胞移植(AHSCT)后 DLBCL 患者的生存情况。我们确定了 62 例 DLBCL 患者,其中 17 例患者最初完全缓解,45 例患者因复发或难治性疾病接受挽救性化疗,随后接受 AHSCT。组织微阵列用针对 GCET1、CD10、BCL6、MUM1、FOXP1 和 LMO2 的单克隆抗体进行免疫染色。使用 Hans 算法,我们将 50%的病例分类为 GCB 型,而 Choi 算法将 58%的病例分类为 GCB 型,并且 LMO2 阳性率为 69%。然而,使用这些方法中的任何一种方法,都没有发现 5 年总生存率或无事件生存率有显著差异。总之,细胞起源不能预测接受 AHSCT 治疗的 DLBCL 患者的生存情况。

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