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供体淋巴细胞输注可使异基因造血干细胞移植后残留或复发的淋巴系统恶性肿瘤患者获得持续缓解。

Donor lymphocyte infusions can result in sustained remissions in patients with residual or relapsed lymphoid malignancy following allogeneic haemopoietic stem cell transplantation.

作者信息

Russell N H, Byrne J L, Faulkner R D, Gilyead M, Das-Gupta E P, Haynes A P

机构信息

Department of Haematology, Nottingham City Hospital, Nottingham, UK.

出版信息

Bone Marrow Transplant. 2005 Sep;36(5):437-41. doi: 10.1038/sj.bmt.1705074.

Abstract

We treated 17 patients with refractory (n = 7) or relapsed lymphoid malignancy (n = 10) following allogeneic HSCT with donor lymphocyte infusions (DLI). Patients with low-grade disease received DLI alone (n = 7) or following radiotherapy (n = 1). Patients with aggressive disease (n = 9) received prior chemotherapy. Nine out of 15 patients receiving DLI from sibling donors responded after one (n = 6), two (n = 2) and three (n = 1) infusions. Both MUD recipients achieved CR after two and three DLI. In all, 10/17 patients achieved CR including 3/4 patients with chronic lymphatic leukaemia (CLL), 4/4 with mantle cell lymphoma (MCL), 3/4 with follicular NHL but 0/5 with aggressive NHL/Richters. The median CD3 cell dose to achieve CR for siblings was 2 x 10(7)/kg. One patient with CLL had a second transplant following DLI-induced aplasia and is in CR at 14 months giving a final CR rate of 64%. Grade II-IV acute GVHD developed in 45% and chronic GVHD in 8/9 evaluable patients. Of the 11 patients finally achieving CR, one patient with MCL relapsed at 18 months post-DLI but all others remain in remission with a median follow-up of 40 months (range 12-64 months). Low-grade NHL and MCL have a high response rate and sustained remissions following DLI. Aggressive disease responds poorly however, despite pre-DLI chemotherapy.

摘要

我们对17例异基因造血干细胞移植(HSCT)后出现难治性(n = 7)或复发性淋巴系统恶性肿瘤(n = 10)的患者进行了供体淋巴细胞输注(DLI)治疗。低度疾病患者单独接受DLI(n = 7)或放疗后接受DLI(n = 1)。侵袭性疾病患者(n = 9)接受过前期化疗。15例接受同胞供体DLI的患者中,9例在1次(n = 6)、2次(n = 2)和3次(n = 1)输注后出现反应。2例无关供体受者在2次和3次DLI后均达到完全缓解(CR)。总计,17例患者中有10例达到CR,其中慢性淋巴细胞白血病(CLL)患者4例中有3例、套细胞淋巴瘤(MCL)患者4例中有4例、滤泡性非霍奇金淋巴瘤(NHL)患者4例中有3例达到CR,但侵袭性NHL/ Richter转化患者5例中无1例达到CR。同胞供体达到CR的CD3细胞中位剂量为2×10⁷/kg。1例CLL患者在DLI诱导的再生障碍性贫血后进行了第二次移植,14个月时处于CR状态,最终CR率为64%。45%的患者发生了II - IV级急性移植物抗宿主病(GVHD),9例可评估患者中有8例发生了慢性GVHD。在最终达到CR的11例患者中,1例MCL患者在DLI后18个月复发,但其他所有患者均保持缓解状态,中位随访时间为40个月(范围12 - 64个月)。低度NHL和MCL对DLI有较高的反应率和持续缓解率。然而,尽管在DLI前进行了化疗,侵袭性疾病的反应较差。

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