Peking University People's Hospital, Peking University Institute of Hematology, Beijing Key Laboratory of Hematopoietic Stem Cell Transplantation, Beijing, China.
Eur J Haematol. 2013 Oct;91(4):304-14. doi: 10.1111/ejh.12168. Epub 2013 Aug 17.
We retrospectively compared the antileukemic effects of chemotherapy alone and chemotherapy followed by modified donor lymphocyte infusion (DLI) in 82 patients with relapsed acute leukemia after haploidentical hematopoietic stem cell transplantation (HSCT) without in vitro T-cell depletion. We also investigated prognostic factors in patients receiving chemotherapy followed by modified DLI. Thirty-two patients received chemotherapy alone, and the remaining 50 patients received chemotherapy followed by modified DLI. In patients receiving chemotherapy followed by modified DLI, complete remission rate was significantly higher (64.0% vs. 12.5%, P = 0.000), the incidence of relapse was significantly lower (50.0% vs. 100.0%, P = 0.000), and disease-free survival was significantly improved (36.0% vs. 0.0%, P = 0.000) compared with patients receiving chemotherapy alone. Multivariate analysis demonstrated that patients with chronic graft-versus-host disease (GVHD) after intervention (P = 0.000) and patients receiving chemotherapy followed by modified DLI (P = 0.037) were associated with a lower relapse rate. Furthermore, in patients receiving chemotherapy followed by modified DLI, multivariate analysis demonstrated that chronic GVHD after modified DLI (P = 0.039) and duration of minimal residual disease (MRD) (-) ≥4 months after modified DLI (P = 0.001) were associated with a lower relapse rate. Our study is the first to suggest that chemotherapy followed by modified DLI is associated with stronger antileukemic effects and better survival in relapsed acute leukemia after haploidentical HSCT without in vitro T-cell depletion. Furthermore, our study suggests that lack of chronic GVHD and duration of MRD (-) <4 months after modified DLI are associated with higher relapse rates in patients receiving chemotherapy followed by modified DLI.
我们回顾性比较了 82 例亲缘半相合造血干细胞移植(HSCT)后未进行体外 T 细胞清除的复发性急性白血病患者接受单纯化疗与化疗后改良供者淋巴细胞输注(DLI)的抗白血病效果,并探讨了接受改良 DLI 化疗患者的预后因素。32 例患者接受单纯化疗,其余 50 例患者接受化疗后改良 DLI。接受改良 DLI 化疗的患者完全缓解率显著较高(64.0%比 12.5%,P=0.000),复发率显著较低(50.0%比 100.0%,P=0.000),无病生存率显著提高(36.0%比 0.0%,P=0.000)。多因素分析显示,干预后慢性移植物抗宿主病(GVHD)患者(P=0.000)和接受改良 DLI 化疗患者(P=0.037)复发率较低。此外,在接受改良 DLI 化疗的患者中,多因素分析显示,改良 DLI 后慢性 GVHD(P=0.039)和改良 DLI 后微小残留病(MRD)(-)≥4 个月(P=0.001)与较低的复发率相关。本研究首次表明,在亲缘半相合 HSCT 后未进行体外 T 细胞清除的复发性急性白血病患者中,化疗后改良 DLI 具有更强的抗白血病作用和更好的生存效果。此外,本研究表明,缺乏慢性 GVHD 和改良 DLI 后 MRD(-)<4 个月与接受改良 DLI 化疗患者的复发率较高相关。