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原发性纵隔大 B 细胞淋巴瘤靶向治疗的当前问题与未来展望

英文原题:Current Issues and Future Perspectives of Targeted Therapies in Primary Mediastinal Large B-Cell Lymphoma.

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Current Issues and Future Perspectives of Targeted Therapies in Primary Mediastinal Large B-Cell Lymphoma.

PubMed 2025/02/11(内容时间) J Clin Med Q1 · IF 3.3(JCR 2025)

分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。

中文摘要

原发性纵隔大B细胞淋巴瘤(PMLBCL)是一种罕见的侵袭性B细胞淋巴瘤,与弥漫性大B细胞淋巴瘤(DLBCL)和霍奇金淋巴瘤(HL)具有共同特征。PMLBCL在一线治疗中通常可通过单打击免疫化疗治愈。复发往往具有侵袭性,且可能对常规化疗无反应。自体干细胞移植(ASCT)对于化疗敏感患者仍是可行选择;然而,靶向治疗似乎极具前景。检查点抑制剂(CPIs)已经改变了复发/难治性疾病的病程,而靶向CD-19的嵌合抗原受体(CAR)T细胞疗法可能产生显著良好的结局。CAR-T 细胞和CPIs在治疗算法中的确切位置,以及放疗和ASCT的作用,仍有待精确确定。在本综述中,我们旨在呈现PMLBCL中靶向药物的最新研究,并确定它们在治疗算法中的排序,主要在复发/难治性背景下。

展开英文摘要原文

Primary mediastinal large B-cell lymphoma (PMLBCL) is a rare, aggressive B-cell lymphoma, sharing common features with diffuse large B-cell lymphoma (DLBCL) and Hodgkin lymphoma (HL). PMLBCL is usually cured with single-hit immunochemotherapy in the first-line setting. Relapses tend to be aggressive and may be unresponsive to conventional chemotherapy. Autologous stem cell transplant (ASCT) remains a viable option for chemosensitive patients; nevertheless, targeted therapies appear to be highly promising.

Checkpoint inhibitors (CPIs) have already transformed the course of relapse/refractory disease, while CD-19-directed Chimeric Antigen Receptor (CAR) T-cell therapy may produce remarkably favorable outcomes. The exact position of CAR T-cells and CPIs in the treatment algorithm, along with the role of radiotherapy and ASCT, remains to be precisely determined. In the current review, we aim to present the recent research on targeted agents in PMLBCL and define their sequencing within the treatment algorithm, mainly in the relapse/refractory setting.

论文信息

作者
Liaskas A、Dimopoulou MN、Piperidou A、Angelopoulou MK、Vassilakopoulos TP
单位
Department of Hematology and Bone Marrow Transplantation, Medical School, National and Kapodistrian University of Athens, General Hospital of Athens "Laikon", 11527 Athens, Greece.Greece
文献类型
综述
期刊
Journal of clinical medicine2025 Feb 11
原文标识
PubMed 40004722 · DOI 10.3390/jcm14041191