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用于华氏巨球蛋白血症(WM)的干细胞移植(SCT)。

Stem cell transplantation (SCT) for Waldenstrom's macroglobulinemia (WM).

作者信息

Anagnostopoulos A, Giralt S

机构信息

Department of Blood and Marrow Transplantation at the University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.

出版信息

Bone Marrow Transplant. 2002 Jun;29(12):943-7. doi: 10.1038/sj.bmt.1703580.

Abstract

Waldenstrom's macroglobulinemia (WM) is a low-grade lymphoplasmacytoid malignancy of unknown etiology. It primarily affects elderly patients and is characterized by a monoclonal IgM component, varying degrees of cytopenias, lymphadenopathy and manifestations related to hyperviscosity syndromes. WM is usually treated with single agent nucleoside analogues or alkylating agents that often provide high response rates and durable remissions. Recurrence of the disease after primary therapy is not uncommon, and resistance to both alkylating agents and nucleoside analogs eventually emerges. Small numbers of patients have undergone high-dose chemotherapy (HDC) with either autologous (n = 24) or allogeneic (n = 6) stem cell transplantation (SCT) as treatment for this disease. Most patients in both groups achieved remission. Results are promising and a more in-depth analysis of possible applications of this treatment modality is attempted with this mini-review.

摘要

华氏巨球蛋白血症(WM)是一种病因不明的低度淋巴浆细胞恶性肿瘤。它主要影响老年患者,其特征为单克隆IgM成分、不同程度的血细胞减少、淋巴结病以及与高黏滞综合征相关的表现。WM通常采用单药核苷类似物或烷化剂治疗,这些药物常常能带来高缓解率和持久缓解。初次治疗后疾病复发并不罕见,并且最终会出现对烷化剂和核苷类似物的耐药。少数患者接受了大剂量化疗(HDC)联合自体(n = 24)或异基因(n = 6)干细胞移植(SCT)来治疗这种疾病。两组中的大多数患者都实现了缓解。结果很有前景,本综述试图对这种治疗方式的可能应用进行更深入的分析。

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