Waldenström的巨球蛋白血症-临床症状和治疗回顾昨天,今天和明天。

Q4 Medicine
Z Adam, L Pour, D Zeman, M Krejčí, I Boichuk, M Krejčí, M Štork, V Sandecká, Z Král
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引用次数: 0

摘要

背景:Waldenström巨球蛋白血症(WM)是一种伴免疫球蛋白M单克隆蛋白的淋巴浆细胞性淋巴瘤。本病发病率极低(0.4/10万),可视为孤儿病。这意味着新药通常会针对更常见的疾病进行测试和注册。目的:本文将重点介绍治疗WM的新药的疗效。结果:目前对症状性WM患者的治疗方案包括烷基化剂环磷酰胺和抗cd20单克隆抗体。与利妥昔单抗、环磷酰胺和地塞米松治疗相比,利妥昔单抗和苯达莫司汀治疗的疗效更长。许多用于多发性骨髓瘤(MM)的药物在多发性骨髓瘤患者身上取得了令人鼓舞的效果。硼替佐米对WM有效,但其神经毒性在WM患者中高于MM患者。因此,一些研究表明,新的蛋白酶体抑制剂卡非佐米和伊唑唑米耐受性更好。新型antid20抗体(obinutuzumab)可用于利妥昔单抗不耐受患者。在我们的5例WM患者中,obinutuzumab和苯达莫司汀比以前的治疗方法达到了更深的反应。口服布鲁顿酪氨酸激酶(BTK)抑制剂伊鲁替尼单独和联合利妥昔单抗扩大了WM患者的治疗选择。新的BTK抑制剂(如;阿卡拉布替尼、扎鲁替尼和维卡布替尼)进行了测试,并记录了它们较低的毒性(心房颤动)。此外,BCL2抑制剂venetoclax是最近测试的。结论:新型antid20抗体(obinutuzumab)对利妥昔单抗不耐受、苯达莫司汀和新型蛋白酶体抑制剂(ixazomib和carfilzomib)或具有较低心脏毒性的新型BTK抑制剂的WM患者具有优势。上述许多药物没有正式注册为WM,只有在卫生保健提供者同意的情况下才能使用。因此,这项工作为它们的功效提供了证据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Waldenström's macroglobulinemia - clinical symptoms and review of therapy yesterday, today and tomorrow.

Background: Waldenström macroglobulinemia (WM) is a lymphoplasmocytic lymphoma with immunoglobulin M monoclonal protein. The incidence of this disease is very low (0.4/100,000), so that this disease can be regarded as an orphan's disease. It means that new drugs are often tested and registered for more frequent diseases.

Purpose: In this review we will focus on the efficacy of the new drugs for WM.

Results: The current treatment options for symptomatic WM patients include alkylating agent cyclophosphamide and anti-CD20 monoclonal antibodies. Therapy with rituximab and bendamustin resulted in longer therapeutic response then therapy with rituximab, cyclophosphamide and dexamethasone. Many drugs, used in multiple myeloma (MM), shoved promising results in WM patients. Bortezomib is effective in WM, but its neurotoxicity is higher in WM than in MM patients. Therefore, new proteasome inhibitors, carfilzomib and ixazomib, are better tolerated as documented in several studies. New types of antiCD20 antibody (obinutuzumab) can be used in patients with rituximab intolerance. in five of our patients with WM, obinutuzumab and bendamustin reached deeper responses than therapies administered in previous lines of therapy. Oral Bruton tyrosine kinase (BTK) inhibitor ibrutinib alone and in combination with rituximab have extended the treatment options for WM patients. New BTK inhibitors (e. g. acalabrutinib, zanubrutinib, and vecabrutinib) were tested and their lower toxicity (atrial fibrillation) was documented. Moreover, the BCL2 inhibitor venetoclax is newly tested.

Conclusion: New antiCD20 antibody (obinutuzumab) is of advantage in patients with WM with rituximab intolerance as well as bendamustin and new proteasome inhibitors (ixazomib and carfilzomib) or new BTK inhibitors with lower cardiotoxicity. Many of the abovementioned drugs do not have official registration for WM and can be administrated with the consent of the health care provider only. Thus, this work brings evidence of their efficacy.

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来源期刊
Klinicka Onkologie
Klinicka Onkologie Medicine-Oncology
CiteScore
1.00
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