布伦妥昔单抗韦多汀在特定患者群体中联合或不联合异体干细胞移植的应用

Q4 Medicine
U. Jäger, F. Keil, M. Hutchings
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引用次数: 0

摘要

虽然联合化疗方案对经典霍奇金淋巴瘤(cHL)和全身性间变性大细胞淋巴瘤(sALCL)有效,但约三分之一的患者在治疗几年内无反应或复发。同种异体干细胞移植(Allogeneic stem cell transplantation, alloSCT)可能在化疗耐药患者中实现长期的疾病控制,但许多患者无法接受同种异体干细胞移植。Brentuximab vedotin (BV)是一种靶向CD30的新型抗体-药物偶联物。最近的数据表明,这种治疗可能对那些对至少两种先前治疗反应不满意且不适合进行同种异体细胞移植的患者有益。此外,BV可用于减轻肿瘤负担,使患者随后进展到允许- sct。本文讨论了难治性cHL和sALCL患者的病例研究,BV为他们提供了持久的完全缓解(cr)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Use of Brentuximab Vedotin with or without Subsequent Allogeneic Stem Cell Transplantation in Selected Patient Groups
Touch MEdical MEdia Abstract While combined chemotherapy regimens can be effective in classical Hodgkin’s lymphoma (cHL) and systemic anaplastic large cell lymphoma (sALCL), around a third of patients are unresponsive or relapse within a few years of treatment. Allogeneic stem cell transplantation (alloSCT) may achieve long-term disease control in patients with chemoresistant disease, but many patients are unable to undergo allo-SCT. Brentuximab vedotin (BV) is a novel antibody-drug conjugate targeting CD30. Recent data have suggested that this treatment may be beneficial in patients who have had an unsatisfactory response to at least two prior treatments and are not eligible for allo-SCT. In addition, BV may be used to reduce tumour burden, allowing patients to subsequently progress to allo-SCT. This article discusses case studies of treatment-refractory patients with cHL and sALCL, for whom BV has provided durable complete responses (CRs).
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来源期刊
European Oncology and Haematology
European Oncology and Haematology Medicine-Hematology
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