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使用阿仑单抗进行缓解诱导可使化疗难治性慢性淋巴细胞白血病(CLL)患者接受异基因干细胞移植。

Remission induction using alemtuzumab can permit chemotherapy-refractory chronic lymphocytic leukemia (CLL) patients to undergo allogeneic stem cell transplantation.

作者信息

Knauf Wolfgang, Rieger Kathrin, Blau Wolfgang, Hegenbart Ute, Von Gruenhagen Ulrich, Niederwieser Dietger, Thiel Eckhard

机构信息

Medical Clinic III - Hematology Oncology and Transfusion Medicine University Clinic Benjamin Franklin of Freie Universitaet Berlin Germany.

出版信息

Leuk Lymphoma. 2004 Dec;45(12):2455-8. doi: 10.1080/10428190400005346.

Abstract

The outcome of allogeneic stem cell transplantation depends upon the disease status before transplantation. Patients with refractory disease are at high risk for relapse. To improve the curative potential of the transplant procedure, we treated 3 chemotherapy-refractory CLL patients with alemtuzumab before allogeneic stem cell transplantation. Prior to therapy, all patients suffered from B-symptoms, and had massive adenopathy, splenomegaly, thrombocytopenia, and anemia; two patients had hepatomegaly. Alemtuzumab greatly reduced tumor mass in blood and bone marrow, B-symptoms resolved, and organomegaly improved. Two patients became blood product independent. All patients proceeded to transplantation after conditioning with TBI 2 Gy (n=1) or Treosulfan (n=2) in combination with Fludarabine either from an HLA-matched sibling (n=2) or from an HLA-matched unrelated donor (n=1). All patients engrafted, and are alive and well. Two patients reached complete remission (CR); one patient attained stable partial remission (PR). These heavily pre-treated refractory patients gained substantial clinical benefit from alemtuzumab, and received successful allografts.

摘要

异基因干细胞移植的结果取决于移植前的疾病状态。难治性疾病患者复发风险很高。为了提高移植手术的治愈潜力,我们在异基因干细胞移植前用阿仑单抗治疗了3例化疗难治性慢性淋巴细胞白血病(CLL)患者。治疗前,所有患者均有B症状,并有大量淋巴结肿大、脾肿大、血小板减少和贫血;2例患者有肝肿大。阿仑单抗大大减少了血液和骨髓中的肿瘤肿块,B症状消失,器官肿大得到改善。2例患者不再依赖血液制品。所有患者在接受2 Gy全身照射(TBI)(n = 1)或曲奥舒凡(n = 2)联合氟达拉滨预处理后进行移植,供体为HLA匹配的同胞(n = 2)或HLA匹配的无关供体(n = 1)。所有患者均成功植入,目前存活且状况良好。2例患者达到完全缓解(CR);1例患者达到稳定部分缓解(PR)。这些经过大量预处理的难治性患者从阿仑单抗中获得了显著的临床益处,并成功接受了同种异体移植。

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