Safety and Effectiveness of Dupilumab in Atopic Dermatitis Patients with Hematologic Comorbidities: A Multicenter, Retrospective Study.

IF 2.7 Q3 IMMUNOLOGY
Antibodies Pub Date : 2025-09-03 DOI:10.3390/antib14030075
Luca Bettolini, Stefano Bighetti, Silvia Mariel Ferrucci, Angelo Valerio Marzano, Francesca Barei, Alessandra Narcisi, Matteo Bianco, Andrea Carugno, Nicola Zerbinati, Simone Ribero, Michela Ortoncelli, Elena Pezzolo, Maddalena Napolitano, Martina Maurelli, Giampiero Girolomoni, Zeno Fratton, Enzo Errichetti, Caterina Foti, Giacomo Dal Bello, Ilaria Trave, Anna Balato, Dario Didona, Niccolò Gori, Federica Veronese, Giovanni Paolino, Franco Rongioletti, Mario Bruno Guanti, Laura Calabrese, Riccardo Balestri, Manfredo Bruni, Mariateresa Rossi
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引用次数: 0

Abstract

Background: Dupilumab, a monoclonal antibody targeting the interleukin-4 receptor α, is approved for moderate-to-severe atopic dermatitis (AD). However, its safety profile in patients with concomitant hematologic disorders remains unclear, as such populations were excluded from pivotal trials.

Objective: To evaluate the safety and effectiveness of dupilumab in adolescents and adults with AD and underlying hematologic comorbidities.

Methods: This retrospective, multicenter study included 139 patients aged ≥15 years with moderate-to-severe AD and at least one hematologic disorder, treated with dupilumab across 21 dermatology centers. Data on disease severity, laboratory markers, and hematologic outcomes were collected over a median follow-up of 52 weeks (range 4-156).

Results: The most common hematologic conditions included monoclonal gammopathies, leukemias, lymphomas, myeloproliferative neoplasms, and immune cytopenias. Clinical response to dupilumab was sustained across all endpoints, with median EASI scores decreasing from 26.0 at the baseline to 1.0 at week 52. NRS pruritus and sleep scores similarly declined to 0.0 by week 52. Serum IgE levels and eosinophil counts progressively decreased. The clinical response to dupilumab was sustained across all endpoints, with significant and progressive improvements in EASI, pruritus NRS, and sleep NRS observed up to week 52, followed by long-term stability through week 156. Serum IgE levels decreased steadily at all timepoints, while eosinophil counts declined after week 4 and stabilized beyond week 52. Hematologic conditions remained stable in 82.7% of patients, resolved in 16.5%, and progressed in only one case. Twelve patients (8.6%) received a new hematologic diagnosis during follow-up; no causal relationship could be established due to the retrospective design and absence of systematic screening, and these findings should be interpreted as descriptive associations only.

Conclusions: Dupilumab appears to be safe and effective in AD patients with a broad range of hematologic comorbidities, including malignancies. These findings support its use in real-world settings, though prospective studies are warranted to further assess long-term safety in this population.

Abstract Image

Dupilumab治疗特应性皮炎伴血液学合并症患者的安全性和有效性:一项多中心回顾性研究
背景:Dupilumab是一种靶向白介素-4受体α的单克隆抗体,已被批准用于治疗中重度特应性皮炎(AD)。然而,其在合并血液病患者中的安全性尚不清楚,因为这类人群被排除在关键试验之外。目的:评价dupilumab治疗阿尔茨海默病和潜在血液学合并症的青少年和成人患者的安全性和有效性。方法:这项回顾性的多中心研究纳入了139例年龄≥15岁的中重度AD患者和至少一种血液系统疾病患者,这些患者接受了21个皮肤科中心的dupilumab治疗。疾病严重程度、实验室标志物和血液学结果的数据在中位随访52周(范围4-156周)期间收集。结果:最常见的血液病包括单克隆伽玛病、白血病、淋巴瘤、骨髓增生性肿瘤和免疫细胞减少症。dupilumab的临床反应在所有终点均持续,EASI评分中位数从基线时的26.0降至第52周时的1.0。到第52周,NRS瘙痒和睡眠评分同样下降到0.0。血清IgE水平和嗜酸性粒细胞计数逐渐下降。dupilumab的临床反应在所有终点均持续,EASI、瘙痒NRS和睡眠NRS的显著进行性改善持续到第52周,随后持续到第156周的长期稳定。血清IgE水平在所有时间点稳定下降,而嗜酸性粒细胞计数在第4周后下降,并在第52周后稳定。82.7%的患者血液学状况保持稳定,16.5%的患者病情缓解,只有1例患者病情进展。12例(8.6%)患者在随访期间出现新的血液学诊断;由于回顾性设计和缺乏系统筛选,无法建立因果关系,这些发现应仅被解释为描述性关联。结论:对于包括恶性肿瘤在内的多种血液合并症的AD患者,Dupilumab似乎是安全有效的。这些发现支持其在现实环境中的使用,尽管需要进一步评估该人群的长期安全性的前瞻性研究。
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来源期刊
Antibodies
Antibodies IMMUNOLOGY-
CiteScore
7.10
自引率
6.40%
发文量
68
审稿时长
11 weeks
期刊介绍: Antibodies (ISSN 2073-4468), an international, peer-reviewed open access journal which provides an advanced forum for studies related to antibodies and antigens. It publishes reviews, research articles, communications and short notes. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. There is no restriction on the length of the papers. Full experimental and/or methodical details must be provided. Electronic files or software regarding the full details of the calculation and experimental procedure - if unable to be published in a normal way - can be deposited as supplementary material. This journal covers all topics related to antibodies and antigens, topics of interest include (but are not limited to): antibody-producing cells (including B cells), antibody structure and function, antibody-antigen interactions, Fc receptors, antibody manufacturing antibody engineering, antibody therapy, immunoassays, antibody diagnosis, tissue antigens, exogenous antigens, endogenous antigens, autoantigens, monoclonal antibodies, natural antibodies, humoral immune responses, immunoregulatory molecules.
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