Mamez A C, Lévy V, Chevallier P, Blaise D, Vigouroux S, Xhaard A, Fegueux N, Contentin N, Beguin Y, Ifrah N, Bulabois C E, Suarez F, Yakoub-Agha I, Turlure P, Deconink E, Lamy T, Cahn J Y, Huynh A, Maury S, Fornecker L M, Ouzegdouh M, Bay J O, Guillerm G, Maillard N, Michallet M, Malfuson J V, Bourhis J H, Rialland F, Oumedaly R, Jubert C, Leblond V, Boubaya M, Mohty M, Nguyen S
Service d'hématologie, Hôpital Saint Antoine, 184 rue du faubourg Saint Antoine, Paris, France.
Unité de Recherche Clinique, Hôpital Avicenne, Bobigny, Cedex, France.
Bone Marrow Transplant. 2016 Mar;51(3):358-64. doi: 10.1038/bmt.2015.280. Epub 2015 Nov 23.
Peripheral T-cell lymphoma carries a poor prognosis. To document a possible graft-versus-lymphoma effect in this setting, we evaluated the impact of immunomodulation in 63 patients with peripheral T-cell lymphoma who relapsed after allogeneic transplant in 27 SFGM-TC centers. Relapse occurred after a median of 2.8 months. Patients were then treated with non-immunologic strategies (chemotherapy, radiotherapy) and/or immune modulation (donor lymphocyte infusions (DLI) and/or discontinuation of immunosuppressive therapy). Median overall survival (OS) after relapse was 6.1 months (DLI group: 23.6 months, non-DLI group: 3.6 months). Among the 14 patients who received DLI, 9 responded and 2 had stable disease. Among the remaining 49 patients, a complete response accompanied by extensive chronic GvHD was achieved in two patients after tapering of immunosuppressive drugs. Thirty patients received radio-chemotherapy, with an overall response rate of 50%. In multivariate analysis, chronic GvHD (odds ratio: 11.25 (2.68-48.21), P=0.0009) and skin relapse (odds ratio: 4.15 (1.04-16.50), P=0.043) were associated with a better response to treatment at relapse. In a time-dependent analysis, the only factor predictive of OS was the time from transplantation to relapse (hazards ratio: 0.33 (0.17-0.640), P=0.0009). This large series provides encouraging evidence of a true GvL effect in this disease.
外周T细胞淋巴瘤预后较差。为了证明在这种情况下可能存在的移植物抗淋巴瘤效应,我们评估了免疫调节对63例外周T细胞淋巴瘤患者的影响,这些患者在27个SFGM-TC中心接受异基因移植后复发。复发发生的中位时间为2.8个月。患者随后接受非免疫策略(化疗、放疗)和/或免疫调节(供体淋巴细胞输注(DLI)和/或停用免疫抑制治疗)。复发后的中位总生存期(OS)为6.1个月(DLI组:23.6个月,非DLI组:3.6个月)。在接受DLI的14例患者中,9例有反应,2例病情稳定。在其余49例患者中,2例在免疫抑制药物减量后出现完全缓解并伴有广泛的慢性移植物抗宿主病(GvHD)。30例患者接受了放化疗,总缓解率为50%。多变量分析显示,慢性GvHD(比值比:11.25(2.68 - 48.21),P = 0.0009)和皮肤复发(比值比:4.15(1.04 - 16.50),P = 0.043)与复发时对治疗的更好反应相关。在时间依赖性分析中,唯一预测OS的因素是从移植到复发的时间(风险比:0.33(0.17 - 0.640),P = 0.0009)。这个大型系列研究为这种疾病中真正的移植物抗淋巴瘤(GvL)效应提供了令人鼓舞的证据。