Popova Tanya Naskova, Radinov Atanass, Stavrov Konstantin, Temelkova Ivanka, Terziev Ivan, Lozev Ilia, Lukanova Detelina, Mangarov Hristo, Wollina Uwe, Tchernev Georgi
Department of Clinical Hematology, University Multiprofile Hospital for Active Treatment "Sveti Ivan Rilski", Sofia 15, Acad. Ivan Geshov Blvd., Sofia 1431, Bulgaria.
Department of Dermatology, Venereology and Dermatologic Surgery, Medical Institute of Ministry of Interior (MVR-Sofia), General Skobelev 79, 1606 Sofia, Bulgaria.
Open Access Maced J Med Sci. 2018 Jul 12;6(7):1275-1277. doi: 10.3889/oamjms.2018.289. eCollection 2018 Jul 20.
Modern drugs could sometimes be a good solution even to problematic patients. The cutaneous and systemic forms of the CD30 positive anaplastic large T-cell lymphoma could often be described as a suitable target for therapy with Brentuximab vedotin.
We present the first case of a Bulgarian patient with a histologically confirmed primary cutaneous T-cell CD30+/ALK- large anaplastic cell lymphoma-cALCL (therapeutically resistant to therapy with Methotrexate, radiation therapy and systemic corticosteroid therapy) who was successfully treated with Brentuximab vedotin. In several years, the patient has developed a comparatively fast skin progression as well as an initial systemic one which impacts inguinal and mediastinal nodes. After the implementation of 4 therapy cycles with Brentuximab vedotin, complete regression of the described by previous hospitalisations lymph nodes as well as 80% reduction of the cutaneous and subcutaneous located tumour formations were observed.
The therapy of CD30+/ALK- anaplastic large T-cell lymphoma is a significant challenge for oncologists and dermatologists because it requires maximally efficient and minimally traumatic treatment in parallel. Therapy with Brentuximab is a new direction which shows extremely good clinical results and can be applied to the cutaneous as well as to the systemic form of anaplastic large-cell CD30 positive lymphoma. The key element by treatment with Brentuximab is suppression of the CD30- expression which, in turn, could be the cause of relapses. On that ground, patients with these lymphomas should be strictly monitored.
现代药物有时甚至对棘手的患者也是一个很好的解决方案。CD30阳性间变性大T细胞淋巴瘤的皮肤型和系统型通常可被描述为用维布妥昔单抗治疗的合适靶点。
我们报告了首例组织学确诊的原发性皮肤T细胞CD30+/ALK-大间变性细胞淋巴瘤(cALCL)(对甲氨蝶呤、放射治疗和全身糖皮质激素治疗耐药)的保加利亚患者,该患者用维布妥昔单抗成功治疗。几年后,患者出现了相对快速的皮肤进展以及最初的系统性进展,累及腹股沟和纵隔淋巴结。在用维布妥昔单抗进行4个治疗周期后,观察到之前住院记录中描述的淋巴结完全消退,以及皮肤和皮下肿瘤形成减少了80%。
CD30+/ALK-间变性大T细胞淋巴瘤的治疗对肿瘤学家和皮肤科医生来说是一项重大挑战,因为它需要同时采用高效且微创的治疗方法。维布妥昔单抗治疗是一个新的方向,显示出极佳的临床效果,可应用于间变性大细胞CD30阳性淋巴瘤的皮肤型和系统型。用维布妥昔单抗治疗的关键因素是抑制CD30表达,而这反过来可能是复发的原因。因此,对这些淋巴瘤患者应进行严格监测。