Hematology Department, Hospital Universitario de Salamanca, IBSAL, CIBERONC, Centro de Investigación del Cáncer-IBMCC (USAL-CSIC), Salamanca, Spain.
Hematology Department, Hospital General Universitario Gregorio Marañón, Madrid, Spain.
Transplantation. 2024 Oct 1;108(10):2134-2143. doi: 10.1097/TP.0000000000005034. Epub 2024 Sep 24.
Chronic graft-versus-host disease (cGVHD) is a cause of late morbidity and nonrelapse mortality (NRM) after allogenic hematopoietic stem cell transplantation (allo-HSCT). Although studies evaluating haploidentical allo-HSCT (haplo-HSCT) using posttransplant cyclophosphamide (PTCy) demonstrate lower cGVHD rates, comprehensive data describing the clinical profile, risk factors, or outcomes of cGVHD within this platform are scarce.
We conducted a retrospective multicenter analysis of 389 consecutive patients who underwent haplo-HSCT PTCy in 7 transplant centers of the Spanish Group Grupo Español de Trasplante Hematopoyético y Terapia Celular (GETH-TC) between 2008 and 2020 describing incidence, clinical profile, risk factors, and cGVHD outcomes.
Ninety-five patients of 389 developed cGVHD. Our data revealed that the incidence and severity of cGVHD are lower than those reported for HLA-identical transplantation with conventional prophylaxis and that the strongest predictor for cGVHD was previous acute GVHD ( P = 0.031). Also, recipient age ≥60 y ( P = 0.044) was protective against cGVHD. Moreover, patients with moderate cGVHD had longer event-free survival at 3 y than other patients ( P = 0.016) and a lower relapse rate at 3 y ( P = 0.036).
Our results support the fact that the incidence and severity of cGVHD are lower than those reported for HLA-identical transplantation with conventional prophylaxis. In this series, patients who develop moderate cGVHD after haplo-HSCT PTCy had a higher overall survival and event-free survival, and lower relapse, suggesting higher graft-versus-leukemia effect. Although this is the largest series focused on characterizing cGVHD in haplo-HSCT PTCy, further prospective studies are needed to confirm the findings.
慢性移植物抗宿主病(cGVHD)是异基因造血干细胞移植(allo-HSCT)后迟发性发病和非复发死亡率(NRM)的原因。虽然评估使用移植后环磷酰胺(PTCy)的半相合 allo-HSCT(haplo-HSCT)的研究显示 cGVHD 发生率较低,但在该平台内描述 cGVHD 的临床特征、危险因素或结果的综合数据却很少。
我们对 2008 年至 2020 年期间在西班牙造血干细胞移植和细胞治疗团体(GETH-TC)的 7 个移植中心接受 haplo-HSCT PTCy 的 389 例连续患者进行了回顾性多中心分析,描述了发生率、临床特征、危险因素和 cGVHD 结果。
389 例中有 95 例患者发生 cGVHD。我们的数据显示,cGVHD 的发生率和严重程度低于传统预防方案下 HLA 匹配移植的报道,cGVHD 的最强预测因素是既往急性移植物抗宿主病(GVHD)(P=0.031)。此外,受体年龄≥60 岁(P=0.044)可预防 cGVHD。此外,在 3 年时,患有中度 cGVHD 的患者无事件生存率高于其他患者(P=0.016),3 年时的复发率较低(P=0.036)。
我们的结果支持这样一个事实,即 cGVHD 的发生率和严重程度低于传统预防方案下 HLA 匹配移植的报道。在本系列中,haplo-HSCT PTCy 后发生中度 cGVHD 的患者总体生存率和无事件生存率更高,复发率更低,提示移植物抗白血病效应更高。尽管这是最大的系列研究旨在描述 haplo-HSCT PTCy 中的 cGVHD,但仍需要进一步的前瞻性研究来证实这些发现。