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首页> 外文期刊>Bone marrow transplantation >Effect of immune modulation in relapsed peripheral T-cell lymphomas after post-allogeneic stem cell transplantation: a study by the Societe Francaise de Greffe de Moelle et de Therapie Cellulaire (SFGM-TC)
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Effect of immune modulation in relapsed peripheral T-cell lymphomas after post-allogeneic stem cell transplantation: a study by the Societe Francaise de Greffe de Moelle et de Therapie Cellulaire (SFGM-TC)

机译:异源性干细胞移植后免疫调节对复发性外周T细胞淋巴瘤的影响:法国社会科学基金会的一项研究(SFGM-TC)

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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.
机译:周围T细胞淋巴瘤预后较差。为了记录在这种情况下可能发生的移植物抗淋巴瘤的作用,我们评估了免疫调节对在27个SFGM-TC中心异基因移植后复发的63例外周T细胞淋巴瘤患者的影响。中位数为2.8个月后发生复发。然后用非免疫策略(化学疗法,放射疗法)和/或免疫调节(供体淋巴细胞输注(DLI)和/或停止免疫抑制疗法)治疗患者。复发后中位总生存期(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,有9例缓解,2例病情稳定。在剩下的49名患者中,在逐渐减少免疫抑制剂后,两名患者获得了完全缓解并伴有广泛的慢性GvHD。 30例患者接受了放化疗,总缓解率为50%。在多变量分析中,慢性GvHD(比值:11.25(2.68-48.21),P = 0.0009)和皮肤复发(比值: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,唯一可预测OS的因素是从移植到复发的时间(危险比:0.33(0.17-0.640),P = 0.0009)。这个大系列文章提供了令人鼓舞的证据,证明这种疾病具有真正的GvL效应。

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