18例非霍奇金淋巴瘤患者首次自体移植失败后的第二次自体移植。

Christelle Lenain, Charles Dumontet, Therese Gargi, Catherine Chassagne, Francoise Berger, David Perol, Maud Garnier, Bertrand Coiffier, Jean Yves Blay
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引用次数: 11

摘要

高剂量化疗和自体骨髓或外周干细胞支持为非霍奇金淋巴瘤(NHL)患者的某些亚组提供了最佳的治愈机会。对于第一次自体移植后复发的患者,第二疗程清髓化疗的作用尚不清楚。本回顾性研究的目的是评估NHL患者第二次自体移植的疾病结局、发病率和死亡率。1985年至2001年间,里昂两家医院接受自体移植治疗的NHL患者中有225人复发。在这225例患者中,18例接受了第二次自体移植。第二次移植的中位年龄为41岁。惰性淋巴瘤6例,侵袭性淋巴瘤12例。第二次移植后的中位随访时间为42个月。2年和5年的总生存率分别为58%和27%。2年和5年的PFS率为36%。5名患者在第二次移植后存活了20到100个月。7例患者死于疾病复发。发生了4例(22%)中毒性死亡:1例肺纤维化,1例真菌感染和心力衰竭,2例急性白血病。少数第一次移植后复发的NHL患者可以通过第二次清髓化疗治愈,但代价是高风险的毒性死亡。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Second autologous transplantation after failure of a first autologous transplant in 18 patients with non-Hodgkin's lymphoma.

High-dose chemotherapy and autologous marrow or peripheral stem cell support offers the best chance of cure in some subgroups of patients with non-Hodgkin's lymphoma (NHL). Less is known about the role of a second course of myeloablative chemotherapy in patients who relapse after a first autologous transplant. The aim of this retrospective study was to evaluate the disease outcome, morbidity and mortality associated with second autologous transplantation in patients with NHL. Between 1985 and 2001, 225 patients who had received autologous transplantation for NHL in two institutions in Lyon relapsed. Of these 225 patients 18 underwent a second autologous transplantation. The median age at second transplant was 41 years. There were six indolent lymphomas and 12 aggressive lymphomas. The median follow-up from the second transplant was 42 months. The OS rate at 2 and 5 years were 58 and 27%, respectively. The PFS rate at 2 and 5 years was 36%. Five patients are alive without disease 20 to 100 months after the second transplant. Seven patients died of disease recurrence. Four (22%) toxic deaths occurred: one of pulmonary fibrosis, one of fungal infection and cardiac failure and two of acute leukaemia. A minority of patients with NHL recurrence after a first transplant can be cured by a second course of myeloablative chemotherapy at the cost however of high-risk toxic death.

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