首页> 美国卫生研究院文献>International Journal of Clinical and Experimental Pathology >A case of post-mogamulizumab relapse of acute-type adult T-cell leukemia/lymphoma successfully treated with mogamulizumab and etoposide
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A case of post-mogamulizumab relapse of acute-type adult T-cell leukemia/lymphoma successfully treated with mogamulizumab and etoposide

机译:莫加莫珠单抗和依托泊苷成功治疗急性型成人T细胞白血病/淋巴瘤的莫加莫珠单抗复发后的情况

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摘要

A 70-year-old man presented to us with the chief complaints of a generalized rash and a mass in the right clavicular region that he first noticed in the year 2012. Biopsy of the mass led to the diagnosis of cutaneous nodular mass-type adult T-cell leukemia/lymphoma (ATLL) in March 2013. Phototherapy was started, and the symptoms improved temporarily. However, in late June 2013, the serum lactate dehydrogenase (LDH) level increased to 358 IU/L, which was 1.6 times higher than the upper limit of the reference range; based on the findings, transformation of the disease to the acute type was diagnosed. The patient was treated with 6 courses of CHOP therapy (cyclophosphamide, doxorubicin, vincristine, and prednisolone), which resulted in complete remission (CR). However, the rash recurred in late October 2013, and treatment with mogamulizumab was initiated. A total of 8 courses of mogamulizumab were administered, which resulted in CR. The rash and cutaneous nodular masses recurred again in January 2014, and a total of 8 courses of mogamulizumab were administered again starting in February 2014. However, the patient’s symptoms began to worsen gradually. Phototherapy was also initiated, but had to be discontinued due to the development of photosensitivity. Treatment with the combination of mogamulizumab and etoposide (25 mg/day for 21 days) was started in May 2014. The nodular mass rapidly decreased in size. The rash or cutaneous nodular mass had not recurred as of August 2014. Thus, combined therapy with mogamulizumab plus etoposide is considered to be effective for resolution of the cutaneous nodular masses in patients with ATLL.
机译:一名70岁的男子向我们展示了他于2012年首次注意到的普遍性皮疹和右锁骨区域肿块的主要主诉。肿块的活检导致皮肤结节性肿块型成人的诊断2013年3月,T细胞白血病/淋巴瘤(ATLL)。开始光疗,症状暂时改善。但是,2013年6月下旬,血清乳酸脱氢酶(LDH)水平增至358 IU / L,是参考范围上限的1.6倍;根据这些发现,诊断出该疾病已转变为急性型。该患者接受了6个疗程的CHOP治疗(环磷酰胺,阿霉素,长春新碱和泼尼松龙),导致完全缓解(CR)。然而,皮疹在2013年10月下旬再次发生,并开始使用Mogamulizumab治疗。总共进行了8个疗程的莫加莫珠单抗治疗,导致CR。皮疹和皮肤结节性肿块在2014年1月再次复发,并且从2014年2月开始再次进行了8个疗程的莫加莫珠单抗治疗。但是,患者的症状开始逐渐恶化。还开始了光疗,但由于光敏性的发展而不得不中止。 2014年5月开始使用莫加莫珠单抗和依托泊苷联合治疗(25 mg /天,共21天)。结节性肿块的大小迅速减少。截至2014年8月,皮疹或皮肤结节性肿块尚未复发。因此,联合使用莫加莫珠单抗加依托泊苷治疗可有效缓解ATLL患者的皮肤结节性肿块。

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