使用 EZH2 抑制剂 tazemetostat 治疗处于白血病期的多发性复发滤泡淋巴瘤,获得完全缓解。

IF 0.5 Q4 ONCOLOGY International Cancer Conference Journal Pub Date : 2024-08-21 eCollection Date: 2024-10-01 DOI:10.1007/s13691-024-00716-z
Shohei Kikuchi, Yoshimi Nabe, Ryusuke Horaguchi, Tomoki Minemura, Jun Murakami, Akira Noguchi, Kohji Takagi, Yusuke Kamihara, Akinori Wada, Takuma Fujihira, Tsutomu Sato
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引用次数: 0

摘要

虽然多次复发和连续缩短缓解期是滤泡性淋巴瘤(FL)的特征之一,但目前尚未确立证据确凿的标准三线和四线治疗方法。Tazemetostat是首个口服酶同源物2(EZH2)增强剂抑制剂,在一项临床试验中,它对复发的突变型EZH2 FL显示出良好的临床疗效和安全性,并被应用于这一临床环境。约10%的FL患者会出现外周血受累,即所谓的白血病期,据报道这是一个不良预后因素。然而,由于EZH2-激活突变并不常见,目前还缺乏他赛莫司他治疗白血病期FL的临床数据。在此,我们报告了一例多次复发的白血病期FL患者,并将他唑司特作为六线治疗药物。塔齐美司他单药治疗在白血病期显示出缓慢而持续的临床疗效,表现为结节受累。治疗 4 个月后,循环淋巴瘤细胞数量逐渐减少并消失。但在治疗 6 个月后,仍能通过流式细胞术检测到循环淋巴瘤细胞,最终在治疗 9 个月后检测不到循环淋巴瘤细胞。他昔莫司他的延长间隔给药可将部分应答转变为完全应答。因此,他赛莫司他对治疗处于白血病期的多发性复发性前列腺癌有效。
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Complete response using the EZH2 inhibitor tazemetostat against multiple relapsed follicular lymphoma in the leukemic phase.

Though multiple relapses and serial shortening of remission is one of the characteristics of follicular lymphoma (FL), standard third- and later-line treatments with clear evidence have not yet been established. Tazemetostat, the first oral enhancer of zester homolog 2 (EZH2) inhibitor, showed a favorable clinical outcome and safety profile against relapsed mutant EZH2 FL in a clinical trial and was applied to this clinical setting. Peripheral blood involvement, known as the leukemic phase, was observed in approximately 10% of patients with FL and reported as a poor prognostic factor. However, because of the infrequency of EZH2-activating mutations, clinical data on tazemetostat against FL in the leukemic phase is lacking. Herein, we report a case of multiple relapsed FL in the leukemic phase for which tazemetostat was administered as a sixth-line treatment. Tazemetostat monotherapy showed a slow and sustained clinical efficacy in the leukemic phase as shown by nodal involvement. Circulating lymphoma cells gradually decreased and disappeared in counts after 4 months of treatment. However, circulating lymphoma cells were still detected by flow cytometry up to 6 months of treatment and finally undetected after 9 months. Extended-interval dosing of tazemetostat transformed a partial response into a complete response. Thus, tazemetostat is effective for the treatment of multiple relapsed FL in the leukemic phase.

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来源期刊
自引率
14.30%
发文量
57
期刊介绍: This online-only journal publishes original case reports on all types of cancer. In particular, we welcome not only case reports of educational value in the diagnosis and treatment of cancers, but also reports on molecularly analyzed cancer cases, including gene mutations, gene fusions, gene expression, and changes in copy number, regardless of their known clinical significance. Assessing the molecular analysis of a tumor usually requires a “cancer conference” in which experts from various fields discuss it. Even if the authors and their respective “cancer conference” were unable to determine the clinical significance of molecular changes at the time of submission and publication, their data may provide evidence that will help the scientific community develop precision medicine solutions in the future. We welcome case reports with reviews of the literature on similar cases, as they are more useful and valuable to readers than are reports of rare cases. International Cancer Conference Journal is the official publication of the Japan Society of Clinical Oncology (JSCO). - Presents an online-only collection of original case reports on all types of cancer - In particular, welcomes molecularly analyzed cancer cases - The Official Publication of the Japan Society of Clinical Oncology (JSCO)
期刊最新文献
HER2-targeted therapy is changing. A case of gastritis caused by immune checkpoint inhibitor treated with infliximab. A case of grade1 follicular lymphoma diagnosed by laparoscopic lymph node resection: differentiating from late lymph node recurrence of endometrial cancer. A case report of mucinous borderline ovarian tumor with recurrence as invasive carcinoma with high copy number alterations. SMARCA4-deficient uterine tumors in young women: response to immune checkpoint inhibitors.
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