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依鲁替尼治疗套细胞淋巴瘤并发进行性多灶性白质脑病

Ibrutinib treatment of mantle cell lymphoma complicated by progressive multifocal leukoencephalopathy
.

作者信息

Mosna Kristina, Ladicka Miriam, Drgona Lubos, Vranovska Martina, Hojsikova Ivana, Tomasova Radka, Danihel Ludovit, Kyselovic Jan, Babal Pavel

出版信息

Int J Clin Pharmacol Ther. 2020 Jun;58(6):343-350. doi: 10.5414/CP203663.

Abstract

OBJECTIVE

Progressive multifocal leukoencephalopathy (PML) is a fatal demyelinating disease of the central nervous system, caused by reactivation of John Cunningham polyomavirus, affecting mainly patients in an immunocompromised state. Recently, drug-associated PML is gaining attention as more cases of PML in connection with the use of various immunomodulatory drugs emerge. Over the last couple of years, sporadic reports have occurred about a possible association between PML and the use of a new immunomodulatory drug, ibrutinib (Imbruvica), primarily indicated for the treatment of various B-cell malignancies.

CASE REPORT

Herein, we report a case of a 62-year-old female patient with bilateral mantle cell lymphoma of conjunctiva diagnosed at IVA clinical stage (according to the Ann Arbor staging of lymphomas) of the disease. As a first line of treatment, the patient was given 6 cycles of rituximab-based chemotherapy followed by a complete remission. Seven years later, the patient relapsed, at which point the treatment with ibrutinib was initiated. Three weeks after the initial dosage, the patient started to show signs of progressive neurological symptomatology and died 4 months thereafter due to bilateral bronchopneumonia. Due to unspecific MRI signs and negative PCR results, the diagnosis of PML was confirmed only postmortem.

CONCLUSION

This case report demonstrates a possible severe adverse effect of the immunomodulatory drug ibrutinib and the importance of a multidisciplinary approach in its diagnosis. Since PML is a rare but highly fatal disease, it is of utmost importance to be aware of the possible connection with the use of this drug to prevent missed or delayed diagnosis, considering that timely therapeutic intervention is crucial for improved prognosis.

摘要

目的

进行性多灶性白质脑病(PML)是一种致命的中枢神经系统脱髓鞘疾病,由约翰·坎宁安多瘤病毒重新激活引起,主要影响免疫功能低下的患者。近年来,随着与各种免疫调节药物使用相关的PML病例增多,药物相关性PML受到了更多关注。在过去几年中,陆续有关于PML与一种新型免疫调节药物伊布替尼(Imbruvica)使用之间可能存在关联的零星报道,伊布替尼主要用于治疗各种B细胞恶性肿瘤。

病例报告

在此,我们报告一例62岁女性患者,诊断为IVA期(根据淋巴瘤的Ann Arbor分期)双侧结膜套细胞淋巴瘤。作为一线治疗,患者接受了6个周期的利妥昔单抗化疗,随后完全缓解。7年后,患者复发,此时开始使用伊布替尼治疗。初始剂量给药三周后,患者开始出现进行性神经症状,4个月后因双侧支气管肺炎死亡。由于MRI表现不特异且PCR结果为阴性,PML诊断仅在尸检后得以证实。

结论

本病例报告证明了免疫调节药物伊布替尼可能存在严重不良反应,以及多学科方法在其诊断中的重要性。由于PML是一种罕见但高度致命的疾病,考虑到及时的治疗干预对改善预后至关重要,认识到与该药物使用的可能关联以防止漏诊或延误诊断极为重要。

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