Espigado I, Ríos E, Marín-Niebla A, Carmona M, Parody R, Pérez-Hurtado J M, Márquez F J, Urbano-Ispizua A
Servicio de Hematología y Hemoterapia, Hospitales Universitarios Virgen del Rocío, Seville, Spain.
Transplant Proc. 2008 Nov;40(9):3104-5. doi: 10.1016/j.transproceed.2008.08.092.
Patients with high-relapse-risk lymphomas or those relapsing after initial therapy have a limited probability of cure with conventional treatment. There is recent inconclusive evidence that, in such cases, intensification or salvage treatment with high-dose chemotherapy followed by hematopoietic stem cell transplantation (HSCT) increases the response rate and may improve survival. Nevertheless, published data on long-term follow-up of high-risk lymphoma patients treated with HSCT are scarce. We analyzed 101 consecutive patients receiving high-dose chemotherapy followed by HSCT after induction with standard chemotherapy. The median age was 38 years (range, 12-63 years). The diagnoses were Hodgkin's disease (n = 32), follicular lymphoma (n = 33), diffuse large B-cell lymphoma (n = 12), mantle cell lymphoma (n = 7), T-cell lymphoma (n = 14), and others (n = 3). Patients received either an autologous graft (n = 72) in first complete remission (1CR; n = 23) or in advanced stages (AS; n = 49), or an allogeneic graft (n = 29) in 1CR (n = 7) or in AS (n = 22). We concluded that transplant-related mortality was 2.7% for patients receiving an autologous HSCT and 27% for patients receiving an allogeneic HSCT. The main etiologies were graft-versus-host disease and infection in the allogeneic setting, and infection in the autologous setting. The probability of long-term (12-year) overall survival was 71%, higher than that described for high-relapse-risk lymphoma patients treated without HSCT and significantly better (P < .05) for patients who received the transplant in 1CR (89%) than in AS (65%). Finally, the probability of long-term survival was significantly better for patients treated with HSCT during the period from 2000-2007 (85%) compared with the period from 1989-1999 (72%).
高复发风险淋巴瘤患者或初始治疗后复发的患者,采用传统治疗治愈的可能性有限。最近有不确定的证据表明,在此类情况下,采用大剂量化疗继以造血干细胞移植(HSCT)进行强化治疗或挽救治疗可提高缓解率,并可能改善生存率。然而,关于接受HSCT治疗的高危淋巴瘤患者长期随访的已发表数据很少。我们分析了101例连续接受标准化疗诱导后进行大剂量化疗继以HSCT的患者。中位年龄为38岁(范围12 - 63岁)。诊断包括霍奇金病(n = 32)、滤泡性淋巴瘤(n = 33)、弥漫性大B细胞淋巴瘤(n = 12)、套细胞淋巴瘤(n = 7)、T细胞淋巴瘤(n = 14)以及其他(n = 3)。患者在首次完全缓解期(1CR;n = 23)或晚期(AS;n = 49)接受自体移植(n = 72),或在1CR(n = 7)或AS(n = 22)接受异基因移植(n = 29)。我们得出结论,接受自体HSCT的患者移植相关死亡率为2.7%,接受异基因HSCT的患者为27%。主要病因在异基因移植情况下为移植物抗宿主病和感染,在自体移植情况下为感染。长期(12年)总生存率为71%,高于未接受HSCT治疗的高复发风险淋巴瘤患者,并且接受移植时处于1CR的患者(89%)显著优于处于AS的患者(65%)(P < 0.05)。最后,与1989 - 1999年期间(72%)相比,2000 - 2007年期间接受HSCT治疗的患者长期生存率显著更好(85%)。