Takai Mika, Shimada Kazuyuki, Furukawa Katsuya, Yamaga Yusuke, Yoshiyama Soichi, Kagaya Yusuke, Suzuki Takashi, Hayashi Kazuhiko, Shimada Satoko, Karube Kennosuke, Kiyoi Hitoshi
Department of Hematology and Oncology, Nagoya University Graduate School of Medicine, Nagoya, Aichi, Japan.
Department of Medical Innovations, Osaka Research Center for Drug Discovery, Otsuka Pharmaceutical Co., Ltd., Minoh, Osaka, Japan.
Cancer Sci. 2025 Jan;116(1):214-225. doi: 10.1111/cas.16310. Epub 2024 Oct 20.
Intravascular large B-cell lymphoma (IVLBCL) is a rare type of extranodal large B-cell lymphoma that is characterized by the proliferation of lymphoma cells in the lumina of small vessels. Recent progress uncovering the genetic characteristics associated with MYD88/CD79B mutations has stimulated interest in the use of drugs targeting B-cell receptor signaling, including Bruton's tyrosine kinase. However, difficulties in culturing ex vivo IVLBCL cells has hampered research on the development of novel therapies. In the present study, we demonstrated the establishment of an ex vivo culture system of IVLBCL cells obtained from patient-derived xenograft (PDX) models. The spheroid culture enabled us to culture IVLBCL PDX cells for more than 10 days and to explore the efficacy of drug treatments acting on these cells. We found that carfilzomib and ibrutinib were effective for treating IVLBCL in ex vivo experiments and conducted in vivo analyses to assess the efficacy of these drugs. Although the efficacy of carfilzomib was difficult to confirm due to its toxicity in our models, ibrutinib showed comparable efficacy to a standard combination of chemotherapy drugs. Together, our data provide a new culture method for IVLBCL PDX cells and a rationale for translating ibrutinib to clinical use in IVLBCL patients.
血管内大B细胞淋巴瘤(IVLBCL)是一种罕见的结外大B细胞淋巴瘤,其特征是淋巴瘤细胞在小血管腔内增殖。最近在揭示与MYD88/CD79B突变相关的遗传特征方面取得的进展激发了人们对使用靶向B细胞受体信号传导的药物(包括布鲁顿酪氨酸激酶)的兴趣。然而,体外培养IVLBCL细胞的困难阻碍了新型疗法开发的研究。在本研究中,我们展示了从患者来源的异种移植(PDX)模型中获得的IVLBCL细胞体外培养系统的建立。球体培养使我们能够培养IVLBCL PDX细胞超过10天,并探索作用于这些细胞的药物治疗效果。我们发现卡非佐米和伊布替尼在体外实验中对治疗IVLBCL有效,并进行了体内分析以评估这些药物的疗效。尽管由于卡非佐米在我们的模型中的毒性,其疗效难以确认,但伊布替尼显示出与标准化疗药物组合相当的疗效。总之,我们的数据为IVLBCL PDX细胞提供了一种新的培养方法,并为将伊布替尼转化为IVLBCL患者的临床应用提供了理论依据。