Ghiso A, Raiola A M, Gualandi F, Dominietto A, Varaldo R, Van Lint M T, Bregante S, Di Grazia C, Lamparelli T, Galaverna F, Stasia A, Luchetti S, Geroldi S, Grasso R, Colombo N, Bacigalupo A
Divisione Ematologia e Trapianto di Midollo, IRCCS San Martino, Genova, Italy.
Clinica Ematologica, IRCSS San Martino, Genova, Italy.
Bone Marrow Transplant. 2015 Jan;50(1):56-61. doi: 10.1038/bmt.2014.217. Epub 2014 Oct 13.
Forty-two patients relapsing after an unmanipulated haploidentical BM transplant and post-transplant CY (PT-CY), were given 108 DLI, with median interval from transplant of 266 days (range, 67-1372). DLI were given at escalating doses, expressed as CD3+ cells/kg, without GVHD prophylaxis, and ranged from 1 × 10(3) to 1 × 10(7) cells/kg (median 5 × 10(5) cells/kg). The average number of DLI per patient was 2.6 (range, 1-6). The diagnosis was leukemias (n=32) grafted with a myeloablative regimen and Hodgkin's disease (n=10), grafted with a nonmyeloablative regimen. Leukemic patients with molecular relapse (n=20), received DLI alone (n=17) or in association with azacytidine (n=3); leukemic patients with hematologic relapse (n=12) received chemotherapy followed by DLI (n=11) or DLI alone (n=1); Hodgkin patients received DLI following 1-3 courses of chemotherapy. In these three groups the incidence of acute GVHD II-III was 15%, 17% and 10%; response rate was 45%, 33% and 70%; 2-year actuarial survival was 43%, 19% and 80% respectively. This study confirms that escalating doses of DLI can be given in the haploidentical setting with PT-CY, with a relatively low risk of acute GVHD. Response rates and survival are dependent on the underlying disease.
42例在未进行处理的单倍体相合骨髓移植及移植后环磷酰胺(PT-CY)治疗后复发的患者,接受了108次供者淋巴细胞输注(DLI),自移植后的中位间隔时间为266天(范围67 - 1372天)。DLI按递增剂量给予,以CD3⁺细胞/千克表示,未进行移植物抗宿主病(GVHD)预防,剂量范围为1×10³至1×10⁷细胞/千克(中位值为5×10⁵细胞/千克)。每位患者接受DLI的平均次数为2.6次(范围1 - 6次)。诊断为采用清髓性方案移植的白血病(n = 32)和采用非清髓性方案移植的霍奇金病(n = 10)。分子复发的白血病患者(n = 20),单独接受DLI(n = 17)或联合阿扎胞苷(n = 3);血液学复发的白血病患者(n = 12)接受化疗后再进行DLI(n = 11)或单独接受DLI(n = 1);霍奇金病患者在接受1 - 3个疗程化疗后接受DLI。在这三组中,急性GVHD II - III级的发生率分别为15%、17%和10%;缓解率分别为45%、33%和70%;2年精算生存率分别为43%、19%和80%。本研究证实,在单倍体相合及PT-CY的情况下,可以给予递增剂量的DLI,急性GVHD风险相对较低。缓解率和生存率取决于基础疾病。