Bernardelli Andrea, Visco Carlo
Hematology Unit, Department of Medicine, Azienda Ospedaliera Universitaria Integrata di Verona, Verona, Italy.
Section of Hematology, Department of Medicine, University of Verona, Piazzale L Scuro, 10, Verona 37134, Italy.
Ther Adv Hematol. 2025 Feb 4;16:20406207251317165. doi: 10.1177/20406207251317165. eCollection 2025.
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.
本报告描述了两例蕈样肉芽肿和塞扎里综合征(MF/SS)患者,他们接受莫加莫单抗联合治疗后获得了临床益处。病例1是一名56岁男性,患有IIIB期(T4NxM0B1)MF,后来进展为SS,伴有持续的皮肤症状(红斑、苔藓化皮肤和瘙痒)以及腋窝和腹股沟淋巴结肿大。针对皮肤和全身的治疗未能使该患者获得持久缓解。莫加莫单抗(1 mg/kg,每周一次,共4周;此后每2周一次)使皮肤症状暂时改善,但约2个月后皮肤病情进展得到确认。随后,莫加莫单抗与补骨脂素加紫外线A(PUVA)联合治疗产生了部分缓解;然而,由于光毒性,PUVA停用,莫加莫单抗继续作为单一疗法使用。在最近一次评估时,持续使用莫加莫单抗单一疗法使皮肤临床症状改善,淋巴结肿大减轻;该患者正在等待异基因造血干细胞移植。病例2是一名80岁男性,患有IIIB期(T4NxM0B1)肉芽肿性变异型MF,表现为弥漫性红斑伴脱屑、睑外翻和腹股沟淋巴结病。口服泼尼松和贝沙罗汀治疗未能获得充分、持久的缓解。莫加莫单抗(1 mg/kg,每周一次,共4周;此后每2周一次)单一疗法最初产生了改善,表现为红斑减轻,但改善未持续。莫加莫单抗加用口服泼尼松,然后加用PUVA;这种联合治疗使皮肤病情得到改善。由于无法获得PUVA,停用了PUVA,并在继续使用莫加莫单抗的同时开始使用甲氨蝶呤(每周10 mg);这使红斑得到改善。在患者死亡前,其临床状况持续改善,继续使用莫加莫单抗加甲氨蝶呤,死亡原因被认为不太可能与治疗有关。我们的经验表明,原则上莫加莫单抗可与其他疗法联合使用;然而,还需要进一步研究。