Sweetenham J W, Taghipour G, Milligan D, Blystad A K, Caballero D, Fassas A, Goldstone A H
CRC Wessex Medical Oncology Unit, University of Southampton, UK.
Bone Marrow Transplant. 1997 Nov;20(9):745-52. doi: 10.1038/sj.bmt.1700963.
The purpose of this study was to investigate the results of high-dose therapy and autologous stem cell transplantation in adult patients with Hodgkin's disease in first relapse after chemotherapy, to determine the overall and progression-free survival, identify prognostic factors for outcome, and to define the role of conventional dose salvage therapy given prior to the high dose regimen. A retrospective analysis of 139 adult patients reported to the lymphoma registry of the European Group for Blood and Marrow Transplantation (EBMT) between February 1984 and July 1995 is considered. Data on all patients were reviewed and prognostic factors determined in univariate analysis. The actuarial 5-year overall survival (OS) and progression-free survival (PFS) for the entire group of 139 patients were 49.4 and 44.7%, respectively. In univariate analysis for OS, disease bulk at the time of high-dose therapy, second-line regimen, initial remission duration and status at transplant had no predictive value. Status at transplant was predictive for OS when patients in second complete remission (CR) were analysed separately from those in chemosensitive relapse. Similar trends were observed for PFS. We concluded that high-dose therapy and autologous stem cell transplantation is an effective strategy for patients with Hodgkin's disease in first relapse after chemotherapy. These results suggest that it should be used regardless of initial remission duration. The role of conventional-dose salvage given prior to high-dose therapy is unclear, since disease status, disease bulk at the time of transplantation, and the second-line regimen had no significant effect on outcome. However, in view of the low patient numbers, no firm conclusion is possible, and this issue requires prospective assessment.
本研究的目的是调查高剂量治疗及自体干细胞移植用于化疗后首次复发的成年霍奇金病患者的效果,确定总生存率和无进展生存率,识别预后因素,并明确在高剂量方案之前给予传统剂量挽救治疗的作用。本研究对1984年2月至1995年7月间向欧洲血液与骨髓移植组(EBMT)淋巴瘤登记处报告的139例成年患者进行了回顾性分析。回顾了所有患者的数据,并在单因素分析中确定了预后因素。139例患者的精算5年总生存率(OS)和无进展生存率(PFS)分别为49.4%和44.7%。在OS的单因素分析中,高剂量治疗时的疾病负荷、二线方案、初始缓解持续时间和移植时的状态无预测价值。当将第二次完全缓解(CR)的患者与化疗敏感复发的患者分开分析时,移植时的状态对OS有预测价值。PFS也观察到类似趋势。我们得出结论,高剂量治疗及自体干细胞移植是化疗后首次复发的霍奇金病患者的有效策略。这些结果表明,无论初始缓解持续时间如何均应采用该治疗方法。高剂量治疗之前给予传统剂量挽救治疗的作用尚不清楚,因为疾病状态、移植时的疾病负荷和二线方案对结局无显著影响。然而,鉴于患者数量较少,无法得出确凿结论,这个问题需要前瞻性评估。