Jo Tatsuro, Sakai Takahiro, Matsuzaka Kaori, Shioya Haruna, Tominaga Hiroo, Kaneko Yohei, Hayashi Shizuka, Matsuo Masatoshi, Taguchi Jun, Abe Kuniko, Shigematsu Kazuto
Department of Hematology, Japanese Red Cross Nagasaki Genbaku Hospital, Nagasaki, Japan.
Department of Laboratory, Japanese Red Cross Nagasaki Genbaku Hospital, Nagasaki, Japan.
Case Rep Oncol. 2020 Nov 30;13(3):1402-1409. doi: 10.1159/000511111. eCollection 2020 Sep-Dec.
We present the case of a 78-year-old male patient who was diagnosed with anaplastic lymphoma kinase (ALK)-negative, CC chemokine receptor 4 (CCR4)-negative, and CD30-positive anaplastic large cell lymphoma (ALCL). The patient had a past medical history of adult T-cell leukemia/lymphoma and colon cancers that had developed simultaneously approximately 2 years prior to the development of ALCL that were treated with immunochemotherapy and resection, respectively. Initial treatment for ALCL included brentuximab vedotin, an anti-CD30 monoclonal antibody-monomethyl auristatin E conjugate; however, we were unable to achieve a sufficient treatment effect. Romidepsin, an oral histone deacetylase inhibitor, was introduced as salvage chemotherapy; complete remission was attained. Interestingly, a reversal of the CD4/CD8 ratio and a reduction in human T-lymphotropic virus type 1 (HTLV-1) virus load was observed after 2 cycles of immunochemotherapy; the patient experienced upregulation of HTLV-1 Tax-specific cytotoxic T lymphocytes after a herpes zoster infection and the completion of immunotherapy. The immunologic status was maintained from the time of diagnosis through the completion of romidepsin therapy. Our findings indicate that romidepsin can be used safely and effectively to treat ALCL without impairing cellular immunity to HTLV-1.
我们报告了一例78岁男性患者,其被诊断为间变性淋巴瘤激酶(ALK)阴性、CC趋化因子受体4(CCR4)阴性且CD30阳性的间变性大细胞淋巴瘤(ALCL)。该患者既往有成人T细胞白血病/淋巴瘤病史,约在ALCL发病前2年同时发生结肠癌,分别接受了免疫化疗和手术切除治疗。ALCL的初始治疗包括使用抗CD30单克隆抗体-单甲基奥瑞他汀E偶联物brentuximab vedotin;然而,我们未能取得足够的治疗效果。口服组蛋白去乙酰化酶抑制剂罗米地辛作为挽救性化疗药物被引入;患者实现了完全缓解。有趣的是,在2个周期的免疫化疗后观察到CD4/CD8比值逆转以及人类T淋巴细胞病毒1型(HTLV-1)病毒载量降低;该患者在带状疱疹感染及免疫治疗完成后,HTLV-1 Tax特异性细胞毒性T淋巴细胞上调。从诊断时起直至罗米地辛治疗结束,免疫状态得以维持。我们的研究结果表明,罗米地辛可安全有效地用于治疗ALCL,而不会损害对HTLV-1的细胞免疫。