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转化型滤泡性淋巴瘤患者自体造血支持的大剂量治疗:来自单一中心的27例患者研究

High-dose therapy with autologous haematopoietic support in patients with transformed follicular lymphoma: a study of 27 patients from a single centre.

作者信息

Foran J M, Apostolidis J, Papamichael D, Norton A J, Matthews J, Amess J A, Lister T A, Rohatiner A Z

机构信息

ICRF Medical Oncology Unit, Department of Medical Oncology, St. Bartholomew's Hospital, London, UK.

出版信息

Ann Oncol. 1998 Aug;9(8):865-9. doi: 10.1023/a:1008349427337.

Abstract

BACKGROUND

The prognosis of patients with transformed follicular lymphoma (FL-t) is poor. The use of high-dose therapy (HDT) with autologous haematopoietic support was therefore evaluated as consolidation of remission.

PATIENTS AND METHODS

Twenty-seven patients received high-dose cyclophosphamide and total body irradiation (cyclo + TBI) with autologous bone marrow (BM; n = 24) or peripheral blood progenitor cell support (PBPC; n = 3). BM was treated in vitro with anti-B cell antibodies and complement. Nineteen of 27 patients were treated in first stable remission following transformation. Eight other patients with a history of transformation were treated following a subsequent recurrence of follicular lymphoma (FL).

RESULTS

With a median follow-up of 2.4 years, 14 of 27 patients remain alive and in remission; five are alive and free of disease at more than four years. The median survival is 8.5 years. There were two 'early' treatment-related deaths of respiratory failure, and two 'late' deaths of myelodysplastic syndrome (MDS) in remission of lymphoma at 2.8 and 8.5 years. Seven of nine patients having had a recurrence underwent re-biopsy. In two, histology revealed FL, in five, transformed follicular lymphoma. One of the patients with recurrent FL is alive without further therapy, and two of five patients with recurrent FL-t are alive and in remission after further chemotherapy.

CONCLUSIONS

It is appropriate to consider HDT for younger patients with FL-t in remission. Repeat biopsy should be considered for patients with recurrent disease. There is a risk of late MDS in patients undergoing this treatment.

摘要

背景

转化型滤泡性淋巴瘤(FL-t)患者的预后较差。因此,评估了采用高剂量疗法(HDT)并辅以自体造血支持作为缓解巩固治疗的效果。

患者与方法

27例患者接受了高剂量环磷酰胺和全身照射(环磷酰胺 + 全身照射),并接受了自体骨髓(BM;n = 24)或外周血祖细胞支持(PBPC;n = 3)。骨髓在体外经抗B细胞抗体和补体处理。27例患者中有19例在转化后首次稳定缓解期接受治疗。另外8例有转化病史的患者在滤泡性淋巴瘤(FL)随后复发后接受治疗。

结果

中位随访2.4年,27例患者中有14例仍存活且处于缓解状态;5例在4年多后存活且无疾病。中位生存期为8.5年。有2例因呼吸衰竭发生“早期”治疗相关死亡,2例在淋巴瘤缓解期2.8年和8.5年时因骨髓增生异常综合征(MDS)发生“晚期”死亡。9例复发患者中有7例接受了再次活检。其中2例组织学显示为FL,5例为转化型滤泡性淋巴瘤。1例复发FL患者未经进一步治疗存活,5例复发FL-t患者中有2例在进一步化疗后存活且处于缓解状态。

结论

对于缓解期的年轻FL-t患者,考虑采用HDT是合适的。复发患者应考虑再次活检。接受该治疗的患者有发生晚期MDS的风险。

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