Christensen Rachel E, Stuver Robert, Dusza Stephen, Epstein-Peterson Zachary D, Ghione Paola, Horwitz Steven M, Johnson William, Moskowitz Alison J, Myskowski Patricia, Pulitzer Melissa, Geller Shamir
Dermatology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.
Lymphoma Service, Department of Medicine, Memorial Sloan Kettering Cancer Center New York, NY.
Clin Lymphoma Myeloma Leuk. 2025 Aug 18. doi: 10.1016/j.clml.2025.08.008.
Mogamulizumab is more effective in treating the blood component of mycosis fungoides (MF) and Sezary syndrome (SS), though some patients also experience significant skin improvement. The characteristics distinguishing those with a favorable skin response remain unclear.
This study aimed to characterize MF/SS patients achieving skin response on mogamulizumab.
A retrospective chart review at a single cancer center included adult MF/SS patients who received at least one mogamulizumab cycle with follow-up. Skin response (≥ 50% clearance) and blood response (≥ 50% decrease in neoplastic cells/µL) were assessed alongside demographics, disease staging, and prior therapies.
Among 56 patients (MF = 35; SS = 21), 43% achieved skin response, with a median time of 2.3 months (range 0.5-6.4). Blood response occurred in 90%, with a median time of 1.8 months (range 0.2-23). Skin-response was highest in patients with blood response (64%), blood disease (B2, 61%), and SS (57%) and was significantly associated with decreasing circulating Sezary cells (P < .001). Among patients without blood involvement (B0), 24% achieved skin response, primarily in erythrodermic cases (71% versus 11%, P = .01).
Mogamulizumab appears effective in inducing skin responses, particularly in advanced-stage and high blood-stage disease. Even in patients without blood compartment involvement, mogamulizumab therapy may still be beneficial, especially for patients with erythroderma. Skin responses are less common in early-stage MF. Patients with both advanced blood and skin disease may benefit from initiating mogamulizumab simultaneously with skin-directed therapy.
莫加莫拉单抗在治疗蕈样肉芽肿(MF)和塞扎里综合征(SS)的血液成分方面更有效,尽管一些患者的皮肤状况也有显著改善。区分那些有良好皮肤反应的患者的特征仍不清楚。
本研究旨在描述在莫加莫拉单抗治疗下实现皮肤反应的MF/SS患者的特征。
在一个单一癌症中心进行的回顾性病历审查纳入了接受至少一个莫加莫拉单抗周期治疗并进行随访的成年MF/SS患者。评估皮肤反应(清除率≥50%)和血液反应(肿瘤细胞/微升减少≥50%)以及人口统计学、疾病分期和既往治疗情况。
在56例患者中(MF = 35例;SS = 21例),43%的患者实现了皮肤反应,中位时间为2.3个月(范围0.5 - 6.4个月)。90%的患者出现血液反应,中位时间为1.8个月(范围0.2 - 23个月)。血液反应患者的皮肤反应率最高(64%),血液疾病患者(B2期,61%)和SS患者(57%)的皮肤反应率也较高,且与循环塞扎里细胞减少显著相关(P < 0.001)。在无血液受累(B0期)的患者中,24%的患者实现了皮肤反应,主要见于红皮病病例(71%对11%,P = 0.01)。
莫加莫拉单抗似乎在诱导皮肤反应方面有效,特别是在晚期和高血液分期疾病中。即使在无血液成分受累的患者中,莫加莫拉单抗治疗可能仍然有益,特别是对于红皮病患者。早期MF患者的皮肤反应较少见。同时患有晚期血液和皮肤疾病的患者可能受益于与皮肤定向治疗同时启动莫加莫拉单抗治疗。