Kiss T L, Panzarella T, Messner H A, Meharchand J, Reddy V, Schimmer A D, Lipton J H
Department of Medical Oncology and Hematology, Princess Margaret Hospital, University of Toronto, Ontario, Canada.
Bone Marrow Transplant. 2003 Jan;31(2):73-8. doi: 10.1038/sj.bmt.1703790.
This study reports on overall and recurrence-free survival (OS and RFS) of 37 consecutive patients with low- and intermediate-grade NHL receiving a related donor allogeneic BMT using a nonradiation-containing preparative regimen. In addition, transplant-related toxicity and factors influencing outcome are discussed. The preparative regimen consisted of busulfan and cyclophosphamide. Median patient age was 44 years (range 20-55). In all, 18 were female. Median follow-up of surviving patients from BMT was 4.2 years. A total of 25 patients had low-grade, and 12 intermediate grade NHL. Most patients (89%) were treated with at least two different chemotherapy regimens prior to BMT. In all, 22 patients (59%) were transplanted in partial remission, 15 (41%) in complete remission. OS at 12 months was 89% (95% confidence interval (CI) of 79-99%) and 79% (64-93%) at 60 months. RFS at 12 months was 86% (75-97%) and at 5 years 70% (54-86%). Four patients (11%) relapsed. Seven patients (19%) died, six because of treatment-related toxicity and one with relapse. Univariate analysis showed improved OS for younger patients and patients of female gender, suggesting that allogeneic BMT using busulfan-cyclophosphamide as a preparative regimen can achieve disease control and possibly cure patients with NHL particularly younger ones.
本研究报告了37例接受相关供体异基因骨髓移植(BMT)的低级别和中级别非霍奇金淋巴瘤(NHL)患者的总生存期(OS)和无复发生存期(RFS),采用的预处理方案不含放疗。此外,还讨论了移植相关毒性和影响预后的因素。预处理方案包括白消安和环磷酰胺。患者中位年龄为44岁(范围20 - 55岁)。共有18例女性。BMT后存活患者的中位随访时间为4.2年。共有25例患者为低级别NHL,12例为中级别NHL。大多数患者(89%)在BMT前接受了至少两种不同的化疗方案。共有22例患者(59%)在部分缓解期接受移植,15例(41%)在完全缓解期接受移植。12个月时的OS为89%(95%置信区间(CI)为79 - 99%),60个月时为79%(64 - 93%)。12个月时的RFS为86%(75 - 97%),5年时为70%(54 - 86%)。4例患者(11%)复发。7例患者(19%)死亡,6例死于治疗相关毒性,1例死于复发。单因素分析显示年轻患者和女性患者的OS有所改善,这表明以白消安 - 环磷酰胺为预处理方案的异基因BMT可以实现疾病控制,并可能治愈NHL患者,尤其是年轻患者。