Denk Alexander, Fante Matthias Alexander, Heidenreich Silke, Greinix Hildegard T, Drouet Eva-Maria Wagner, Egger-Heidrich Katharina, Marx Julia, Kodzhabasheva Darina, Krüger William, Bug Gesine, Wehr Claudia, Halter Joerg, von Lüttichau Irene Teichert, Mueller Lutz Peter, Penack Olaf, Hilgendorf Inken, Kobbe Guido, Klein Stefan, Lawitschka Anita, Frietsch Jochen, Winkler Julia, Wolff Daniel
Internal Medicine III - Hematology and Oncology, University Hospital Regensburg, Regensburg, Germany.
Internal Medicine III - Hematology and Oncology, University Hospital Regensburg, Regensburg, Germany.
Transplant Cell Ther. 2025 Jul;31(7):450.e1-450.e10. doi: 10.1016/j.jtct.2025.04.017. Epub 2025 May 5.
Chronic graft-versus-host disease (cGVHD) represents a major complication after allogeneic stem cell transplantation (alloHSCT). In 2009 and 2018 a survey among German, Austrian, and Swiss transplant centers showed a homogeneous 1-line treatment practice, while 2nd-line treatment as well as management of progressive onset type and bronchiolitis obliterans syndrome (BOS) displayed significant heterogeneity. Since the last survey, ruxolitinib (rux) has been approved and other new agents are explored in treatment of cGVHD.
We conducted a follow-up survey in 2024 to document the impact of recent approvals and new agents on treatment pattern focusing on management of 2nd-line treatment, progressive onset type, BOS, and sclerotic manifestations.
A paper-and-pencil-based questionnaire was sent electronically to 60 German speaking centers performing alloHSCT. 20 centers responded, representing 45% of the patients receiving an alloHSCT in 2023 in Germany, Austria, and Switzerland.
In 1-line treatment of classic standard risk cGVHD, single agent prednisone represents standard of care (14/20 centers) which may be combined with calcineurin inhibitor (CNI) (4/20), while rux is used in selected cases only. In 2nd-line treatment rux is now used by the majority of centers (19/20). In the presence of cytopenia, rux remains the preferred agent (12/20) while use of extracorporeal photopheresis (ECP) is considered by 8 of 20 centers. In case of active infections, ECP is preferred by 15 of 20 centers and both agents are regarded as steroid-sparing agents in 2nd-line treatment of steroid-dependent cGVHD. Rux would be applied in the presence of active infections by 5/20 centers only. Moreover, rux (15/20) and ECP (6/20) are also preferred treatment modalities in treatment of progressive onset cGVHD. For BOS, systemic and inhalative corticosteroids, montelukast and azithromycin (FAM, 13/20), rux (15/20), ECP (17/20) and CNI (10/20) are frequently applied agents, while abatacept (8/20), belumosudil (7/20), imatinib (5/20), mycophenolate mofetil (MMF) (5/20), everolimus (4/20) and ibrutinib (3/20) are used as salvage options in selected patients only. In case of new sclerotic manifestations after failure of 2nd-line treatment including steroids, CNI and rux, most centers would use ECP (14/20), whereas subsequent or alternative salvage treatment of sclerotic manifestations remains heterogenous comprising belumosudil (13/20), ibrutinib (5/20), imatinib (5/20), rituximab (4/20), cyclosporine (3/20), tacrolimus (3/20), everolimus (3/20), sirolimus (3/20), methotrexate (3/20) and MMF (3/20). The preferred taper sequence of immunosuppressive agents in case of response applied in 12/20 centers is initial taper of steroids, followed by taper of CNI and final termination of rux.
The survey documents the effect of evidence and approval on clinical care with single agent prednisone representing the standard of care in 1-line treatment while rux combined with steroids defines the new standard for 2-line treatment of cGVHD. ECP is used in case of contraindication for rux and both agents are also used in progressive onset cGVHD. In contrast, treatment of BOS and sclerotic cGVHD beyond 2-line treatment remains heterogeneous with new agents being integrated in the treatment landscape.
慢性移植物抗宿主病(cGVHD)是异基因干细胞移植(alloHSCT)后的主要并发症。2009年和2018年在德国、奥地利和瑞士移植中心进行的一项调查显示,一线治疗方案较为统一,而二线治疗以及进行性发病型和闭塞性细支气管炎综合征(BOS)的管理则存在显著异质性。自上次调查以来,芦可替尼(rux)已获批准,并且正在探索其他新药物用于治疗cGVHD。
我们在2024年进行了一项随访调查,以记录近期获批药物和新药物对治疗模式的影响,重点关注二线治疗、进行性发病型、BOS和硬化表现的管理。
通过电子方式向60个德语区中心发送了纸质问卷。20个中心做出了回应,占2023年德国、奥地利和瑞士接受alloHSCT患者的45%。
在经典标准风险cGVHD的一线治疗中,单药泼尼松是标准治疗方案(14/20个中心),可与钙调神经磷酸酶抑制剂(CNI)联合使用(4/20),而芦可替尼仅在特定情况下使用。在二线治疗中,现在大多数中心使用芦可替尼(19/20)。在存在血细胞减少的情况下,芦可替尼仍然是首选药物(12/20),而20个中心中有8个考虑使用体外光化学疗法(ECP)。在有活动性感染的情况下,20个中心中有15个首选ECP,并且在依赖类固醇的cGVHD二线治疗中,这两种药物都被视为类固醇节省药物。只有5/20个中心会在有活动性感染时应用芦可替尼。此外,芦可替尼(15/20)和ECP(6/20)也是进行性发病型cGVHD的首选治疗方式。对于BOS,全身和吸入性皮质类固醇、孟鲁司特和阿奇霉素(FAM,13/20)、芦可替尼(15/20)、ECP(17/20)和CNI(10/20)是常用药物,而阿巴西普(8/20)、贝利司他(7/20)、伊马替尼(5/20)、霉酚酸酯(MMF)(5/20)、依维莫司(4/20)和伊布替尼(3/20)仅在特定患者中用作挽救治疗选择。在二线治疗(包括类固醇、CNI和芦可替尼)失败后出现新的硬化表现时,大多数中心会使用ECP(14/20),而硬化表现的后续或替代挽救治疗仍然存在异质性,包括贝利司他(13/20)、伊布替尼(5/20)、伊马替尼(5/20)、利妥昔单抗(4/20)、环孢素(3/20)、他克莫司(3/20)、依维莫司(3/20)、西罗莫司(3/20)、甲氨蝶呤(3/20)和MMF(3/20)。12/20个中心在免疫抑制剂出现反应时首选的减量顺序是先减类固醇,然后减CNI,最后停用芦可替尼。
该调查记录了证据和获批药物对临床治疗的影响,单药泼尼松是一线治疗的标准治疗方案,而芦可替尼联合类固醇定义了cGVHD二线治疗的新标准。在芦可替尼禁忌的情况下使用ECP,并且这两种药物也用于进行性发病型cGVHD。相比之下,二线治疗后的BOS和硬化性cGVHD的治疗仍然存在异质性,新药物正在融入治疗格局。