伊鲁替尼加R-ICE诱导伴有中枢神经系统复发的囊胚变异性套细胞淋巴瘤缓解。

IF 0.7 Q4 HEMATOLOGY
Timothy S Oh, Madelyn Burkart, Amir Behdad, Hatice Savas, Reem Karmali
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引用次数: 2

摘要

套细胞淋巴瘤(MCL)是一种侵袭性的,难以治疗的淋巴瘤亚型,导致复发和预后差。布鲁顿酪氨酸激酶(BTK)抑制剂等新型药物已被研究用于治疗复发/难治性(R/R) MCL。特别是BTK抑制剂ibrutinib,已被证明可以改善R/R MCL的生存结果。尽管取得了这些进展,但许多MCL病例,包括更具侵袭性的囊胚和多形性变异,将经历疾病进展,导致较差的生存结果。囊胚变异型MCL与中枢神经系统(CNS)受累风险增加相关,导致高死亡率。在这个病例报告中,我们讨论了一个被诊断为囊虫性MCL并伴有中枢神经系统复发的患者,在接受标准的利妥昔单抗加异环磷酰胺-卡铂-依托泊苷(R-ICE)补救性化疗加上伊鲁替尼后获得了完全缓解(CR)。患者随后接受了自体干细胞移植(autoSCT),并使用依鲁替尼维持CR。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Ibrutinib Plus R-ICE Induces Remission in Blastoid Variant Mantle Cell Lymphoma with CNS Relapse.

Ibrutinib Plus R-ICE Induces Remission in Blastoid Variant Mantle Cell Lymphoma with CNS Relapse.

Ibrutinib Plus R-ICE Induces Remission in Blastoid Variant Mantle Cell Lymphoma with CNS Relapse.

Mantle cell lymphoma (MCL) is an aggressive, difficult to treat subtype of lymphoma, resulting in relapses and poor outcomes. Novel agents such as Bruton tyrosine kinase (BTK) inhibitors have been studied in the treatment of relapsed/refractory (R/R) MCL. BTK inhibitor ibrutinib, in particular, has demonstrated improvement in survival outcomes of R/R MCL. Despite these advancements, many cases of MCL, including the more aggressive blastoid and pleomorphic variants, will undergo disease progression leading to poor survival outcomes. Blastoid variant MCL is associated with an increased risk of central nervous system (CNS) involvement, causing high mortality rates. In this case report, we discuss a patient with a diagnosis of blastoid MCL with CNS relapse who achieved a complete response (CR) after receiving standard rituximab plus ifosfamide-carboplatin-etoposide (R-ICE) salvage chemotherapy with the addition of ibrutinib. The patient subsequently underwent autologous stem cell transplantation (autoSCT) and maintained CR with ibrutinib maintenance.

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