Division of Stem Cell Transplantation and Immunotherapy, University of Kiel, Kiel, Germany.
Biol Blood Marrow Transplant. 2013 Nov;19(11):1632-7. doi: 10.1016/j.bbmt.2013.07.003. Epub 2013 Jul 11.
Patients with relapsed or refractory advanced T cell non-Hodgkin lymphoma have a dismal prognosis and may not even reach allogeneic hematopoietic stem cell transplantation (HSCT) in adequate condition. We present the outcome of 24 consecutive patients (age range 11 to 65 years) treated at a single institution in Kiel within a recent 5.5-year time frame with allogeneic HSCT in a rather uniform approach. Relapsed and refractory T and natural killer cell lymphomas of various subtypes were included. All patients except 1 were in progression or relapse before start of pretransplantation salvage therapy. Five patients had relapsed after autologous HSCT. With intensive remission induction therapy, usually the CLAEG (cladribine, cytosine arabinoside, and etoposide with granulocyte colony-stimulating factor support) protocol, attempts were made to improve disease control and proceed immediately to conditioning with carmustine, etoposide, cytosine arabinoside, melphalan (BEAM), and medium-dose alemtuzumab. Twenty of 21 patients who received CLAEG induction therapy benefited from this protocol and 1 patient appeared to be therapy-resistant. At the time of allogeneic HSCT, 9 patients were in complete remission (CR) (2 in CR1, 5 in CR2, and 2 in CR >2), whereas 50% had never achieved CR. Nineteen transplants were obtained from matched or partially matched unrelated donors and only 5 from siblings. With a median follow-up of 321 days (1252 days for surviving patients), 20 of 22 assessable patients reached CR. Five of these patients had hematologic or molecular relapse. With donor lymphocyte infusions, 1 patient became minimal residual disease MRD negative again and has maintained CR for more than 4 years. The frequency of grades II to IV acute graft-versus-host disease was 25% and chronic graft-versus-host disease, 30%. Intense reinduction therapy followed by reduced-intensity BEAM-alemtuzumab conditioning and allogeneic HSCT is effective and offers curative potential for patients with advanced T cell lymphomas, even for those not in remission.
24 例复发或难治性晚期 T 细胞非霍奇金淋巴瘤患者在单一机构接受同种异体造血干细胞移植(HSCT)的结果。这些患者在最近 5.5 年的时间内接受了治疗,采用了相对统一的方法。包括各种亚型的复发和难治性 T 细胞和自然杀伤细胞淋巴瘤。除 1 例患者外,所有患者在开始移植前挽救性治疗前均处于进展或复发状态。5 例患者在自体 HSCT 后复发。通过强化缓解诱导治疗,通常采用 CLAEG(克拉屈滨、阿糖胞苷和依托泊苷联合粒细胞集落刺激因子支持)方案,试图改善疾病控制并立即进行卡莫司汀、依托泊苷、阿糖胞苷、马法兰(BEAM)和中剂量阿仑单抗预处理。21 例接受 CLAEG 诱导治疗的患者中有 20 例从中受益,1 例患者似乎对治疗有抵抗。在接受同种异体 HSCT 时,9 例患者处于完全缓解(CR)状态(2 例 CR1,5 例 CR2,2 例 CR>2),而 50%的患者从未达到 CR。19 例移植来自匹配或部分匹配的无关供体,只有 5 例来自兄弟姐妹。中位随访 321 天(存活患者随访 1252 天),22 例可评估患者中有 20 例达到 CR。其中 5 例患者出现血液学或分子复发。通过供者淋巴细胞输注,1 例患者再次达到微小残留病(MRD)阴性并维持 CR 超过 4 年。II 级至 IV 级急性移植物抗宿主病的发生率为 25%,慢性移植物抗宿主病的发生率为 30%。强化再诱导治疗后采用减低强度 BEAM-阿仑单抗预处理和同种异体 HSCT 对晚期 T 细胞淋巴瘤患者有效,具有治愈潜力,即使对于未缓解的患者也是如此。