Management of mycosis fungoides and Sézary syndrome with mogamulizumab in combination with psoralen plus UVA: two case reports.

IF 3.4 3区 医学 Q2 HEMATOLOGY
Therapeutic Advances in Hematology Pub Date : 2025-02-04 eCollection Date: 2025-01-01 DOI:10.1177/20406207251317165
Andrea Bernardelli, Carlo Visco
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引用次数: 0

Abstract

This report describes the cases of two patients with mycosis fungoides and Sézary syndrome (MF/SS) who achieved clinical benefit with mogamulizumab combination therapies. Case 1 is a 56-year-old male with stage IIIB (T4NxM0B1) MF, which later progressed into SS, with ongoing skin symptoms (erythema, lichenified skin, and pruritis) and axillary and inguinal lymphadenomegaly. Skin-directed and systemic therapies failed to achieve a long-lasting response in this patient. Mogamulizumab (1 mg/kg once weekly for 4 weeks; once every 2 weeks thereafter) yielded temporary improvement in skin symptoms, but progression in the skin was confirmed after ~2 months. Subsequently, the combination of mogamulizumab with psoralen plus ultraviolet light A (PUVA) yielded a partial response; however, PUVA was discontinued due to phototoxicity and mogamulizumab was continued as monotherapy. At the latest evaluation, clinical improvement in the skin and reduced lymphadenomegaly were evident with ongoing mogamulizumab monotherapy; the patient is awaiting allogeneic hematopoietic stem cell transplantation. Case 2 is an 80-year-old male with stage IIIB (T4NxM0B1) granulomatous variant MF who presented with diffuse erythema with desquamation, ectropion, and inguinal lymphadenopathy. Treatment with oral prednisone and bexarotene failed to achieve adequate, long-lasting responses. Mogamulizumab (1 mg/kg once weekly for 4 weeks; once every 2 weeks thereafter) monotherapy yielded an initial improvement, characterized by less intense erythema, but the improvement was not sustained. Mogamulizumab was supplemented with oral prednisone and then PUVA; this combination resulted in improvement in the skin. PUVA was stopped due to unavailability, and methotrexate (10 mg once weekly) was initiated alongside continued mogamulizumab; this led to improvement in erythema. The patient continued mogamulizumab plus methotrexate with improving clinical status, prior to their death, which was deemed to be unlikely to be related to treatment. Our experience suggests that, in principle, mogamulizumab can be used in combination with other therapies; however, further research is needed.

mogamulizumab联合补骨脂素+ UVA治疗蕈样真菌病和ssamzary综合征:2例报告
本报告描述了两例真菌样霉菌病和ssamzary综合征(MF/SS)患者通过mogamulizumab联合治疗获得临床获益的病例。病例1为56岁男性,IIIB期(T4NxM0B1) MF,后来发展为SS,伴有持续的皮肤症状(红斑、皮肤苔藓化和瘙痒)以及腋窝和腹股沟淋巴结肿大。皮肤定向和全身治疗未能在该患者中取得持久的反应。莫gamulizumab (1mg /kg,每周1次,共4周;此后每2周1次)皮肤症状暂时改善,但2个月后确认皮肤进展。随后,mogamulizumab联合补骨脂素+紫外光A (PUVA)产生部分反应;然而,由于光毒性,PUVA被停药,mogamulizumab继续作为单药治疗。在最新的评估中,持续的mogamulizumab单药治疗明显改善了皮肤和减少了淋巴肿大;患者正在等待异体造血干细胞移植。病例2是一名80岁男性,患有IIIB期(T4NxM0B1)肉芽肿变异性MF,表现为弥漫性红斑伴脱屑、外翻和腹股沟淋巴结病。口服强的松和贝沙罗汀治疗未能达到充分、持久的疗效。莫gamulizumab (1mg /kg,每周1次,共4周;此后每2周一次)单药治疗取得了初步改善,其特点是红斑不那么强烈,但改善并没有持续下去。莫gamulizumab组先口服强的松,再口服PUVA;这种组合导致了皮肤的改善。由于无法获得PUVA,停用甲氨蝶呤(每周一次,10mg),同时继续使用莫加单抗;这导致了红斑的改善。患者在死亡前继续服用mogamulizumab加甲氨蝶呤,临床状况有所改善,被认为不太可能与治疗有关。我们的经验表明,原则上,mogamulizumab可以与其他疗法联合使用;然而,还需要进一步的研究。
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来源期刊
CiteScore
4.30
自引率
0.00%
发文量
54
审稿时长
7 weeks
期刊介绍: Therapeutic Advances in Hematology delivers the highest quality peer-reviewed articles, reviews, and scholarly comment on pioneering efforts and innovative studies across all areas of hematology. The journal has a strong clinical and pharmacological focus and is aimed at clinicians and researchers in hematology, providing a forum in print and online for publishing the highest quality articles in this area.
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