Muhsen Ibrahim N, Niederwieser Dietger, Garderet Laurent, Penack Olaf, Greinix Hildegard T, El Fakih Riad, Abdeljelil Nour Ben, Abosoudah Ibraheem, Alamoudi Sameer, Albeihany Amal, Al Daama Saad Ahmed, Alshahrani Mohammad Hamad, Alshemmari Salem, Al-Khabori Murtadha, Almasari Ahlam, Al Rawas Abdulhakim, Askar Medhat, Bazarbachi Ali, Bekadja Mohammed-Amine, Benakli Malek, Borhany Munira, Kababri Maria El, Halahleh Khalid, Hamidieh Amir Ali, Hammad Mahmoud, Ibrahim Ahmad, Kanfar Solaf, Khalaf Mohamed Hamed, Marei Mohammed, Mir Muhammad Ayaz, Monagel Dania, Quessar Asma, Rihani Rawad, Shabbir-Moosajee Munira, Shaheen Marwan, Sultan Almetwaly Mohamed, Vaezi Mohammad, Rondelli Damiano, Koh Mickey Boon Chai, Peric Zina, Atsuta Yoshiko, Chaudhri Naeem, Aljurf Mahmoud
Section of Hematology and Oncology, Department of Medicine, Baylor College of Medicine, Houston, TX, USA.
University Hospital Leipzig, Leipzig, Germany.
Hematol Oncol Stem Cell Ther. 2025;18(2):79-85. doi: 10.4103/hemoncstem.HEMONCSTEM-D-25-00005. Epub 2025 Jun 20.
The treatment of acute and chronic graft-versus-host disease (GvHD) remains a challenge, particularly in cases of steroid-refractory GvHD. The management of GvHD varies between institutions, and little is known regarding the practices in different regions of the world. Thus, the Worldwide Network for Blood and Marrow Transplantation has developed a questionnaire to understand the current practices of GvHD management in the Eastern Mediterranean (EM) region.
The questionnaire had 46 items and was distributed electronically to transplant centers in the EM region. Responses were received between December 2022 and June 2023. The questionnaire addressed the management of acute and chronic GvHD for both newly diagnosed and refractory cases.
The questionnaire was completed by 30 programs across 26 institutions located in 11 countries. For patients with newly diagnosed acute GvHD, most programs reported the use of systemic steroids for initial treatment, with doses selected based on the severity of the presentation: the equivalent of 1 mg/kg/day of prednisone for grade IIa and 2 mg/kg/day for grade IIb. In addition to steroids, most programs continued immunosuppressive therapy or reintroduced it if GvHD developed after its cessation. For patients who were refractory to steroids, ruxolitinib was the most frequently selected second-line treatment, chosen by 80% of the programs, followed by calcineurin inhibitors (47%), high-dose steroids (>2 mg/kg, 43%), mycophenolate mofetil (MMF, 40%), and extracorporeal photopheresis (ECP, 40%). On the other hand, for patients with newly diagnosed chronic GvHD, systemic steroids are used for the initial management of mild chronic GvHD not accessible by topical treatment and moderate to severe disease, with the most commonly used initial dose being the equivalent of 0.5 to 1 and >1 mg/kg/day of prednisone, respectively. More than two-thirds of the programs use another agent in addition to steroids in patients who develop moderate/severe chronic GvHD while off immunosuppressive therapy. For patients with steroid-refractory chronic GvHD, most programs selected multiple options in the second-line setting, with the most frequently selected options being ruxolitinib (77%), calcineurin inhibitors (68%), MMF (53%), imatinib (53%), ECP (50%), rituximab (47%), and ibrutinib (40%).
Our results demonstrated that GvHD management practices in the EM region generally align with current guidelines. However, the results highlight that access to clinical trials and multidisciplinary support teams remains limited.
急性和慢性移植物抗宿主病(GvHD)的治疗仍然是一项挑战,尤其是在类固醇难治性GvHD病例中。GvHD的管理在不同机构之间存在差异,对于世界不同地区的实践了解甚少。因此,全球血液和骨髓移植网络开发了一份问卷,以了解东地中海(EM)地区GvHD管理的当前实践。
该问卷有46个项目,通过电子方式分发给EM地区的移植中心。在2022年12月至2023年6月期间收到了回复。该问卷涉及新诊断和难治性病例的急性和慢性GvHD的管理。
来自11个国家26个机构的30个项目完成了问卷。对于新诊断的急性GvHD患者,大多数项目报告使用全身类固醇进行初始治疗,剂量根据临床表现的严重程度选择:IIa级相当于1mg/kg/天的泼尼松,IIb级相当于2mg/kg/天。除类固醇外,如果在停用免疫抑制治疗后发生GvHD,大多数项目会继续或重新引入免疫抑制治疗。对于对类固醇难治的患者,芦可替尼是最常选择的二线治疗药物,80%的项目选择了它,其次是钙调神经磷酸酶抑制剂(47%)、高剂量类固醇(>2mg/kg,43%)、霉酚酸酯(MMF,40%)和体外光化学疗法(ECP,40%)。另一方面,对于新诊断的慢性GvHD患者,全身类固醇用于局部治疗无法触及的轻度慢性GvHD以及中度至重度疾病的初始管理,最常用的初始剂量分别相当于0.5至1mg/kg/天和>1mg/kg/天的泼尼松。超过三分之二的项目在停用免疫抑制治疗后发生中度/重度慢性GvHD的患者中,除类固醇外还使用另一种药物。对于类固醇难治的慢性GvHD患者,大多数项目在二线治疗中选择多种方案,最常选择的方案是芦可替尼(77%)、钙调神经磷酸酶抑制剂(68%)、MMF(53%)、伊马替尼(53%)、ECP(50%)利妥昔单抗(47%)和伊布替尼(40%)。
我们的结果表明,EM地区的GvHD管理实践总体上与当前指南一致。然而,结果突出表明,获得临床试验和多学科支持团队的机会仍然有限。