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首页> 外文期刊>European Journal of Haematology >Combination therapy incorporating Bcl‐2 inhibition with Venetoclax for the treatment of refractory primary plasma cell leukemia with t (11;14)
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Combination therapy incorporating Bcl‐2 inhibition with Venetoclax for the treatment of refractory primary plasma cell leukemia with t (11;14)

机译:将Bcl-2抑制的组合疗法用嘌呤醛糖抑制用于治疗难治性原发性浆细胞白血病(11; 14)

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摘要

Abstract Primary plasma cell leukemia ( pPCL ) is the most aggressive form of the plasma cell ( PC ) malignancy, multiple myeloma ( MM ). It has been commonly associated with the presence of a chromosome translocation involving the immunoglobulin heavy chain (IgH) locus on 14q32, that is t (11;14). Results from early phase clinical trials utilizing the selective Bcl‐2 inhibitor, venetoclax, as a single agent in patients with relapsed MM have had remarkable efficacy among patients with t (11;14) abnormality. The present case demonstrates the ability of a combination regimen incorporating Bcl‐2 inhibition with daratumumab, bortezomib, venetoclax, and dexamethasone to induce a rapid and very deep hematologic response in a pPCL patient with t (11;14), even in a setting of very refractory disease. This case highlights the need to further study Bcl‐2 inhibition‐based therapy as an option for therapy in patients with pPCL with t (11;14).
机译:摘要初级血浆细胞白血病(PPCL)是血浆细胞(PC)恶性肿瘤,多发性骨髓瘤(MM)的最具侵略性形式。 它通常与涉及14Q32上的免疫球蛋白重链(IGH)基因座的染色体易位存在,即T(11; 14)。 利用选择性Bcl-2抑制剂,veretoclax的早期临床试验结果,作为复发mm的患者的单一剂,T(11; 14)异常的患者具有显着的疗效。 本病例证明了将Bcl-2抑制的组合方案与达拉穆曼,硼卓·米布,嘌呤菌和地塞米松和地塞米松的能力表明,即使在型号中 非常难治性疾病。 这种情况突出了进一步研究基于BCL-2抑制的疗法作为PPC1患者的选择,具有T(11; 14)的选择。

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