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异环磷酰胺与米托蒽醌(I-M)治疗复发性高级别非霍奇金淋巴瘤和霍奇金病的双轨研究。约克郡地区淋巴瘤组和中央淋巴瘤组。

Twin-track studies of ifosfamide and mitoxantrone (I-M) in recurrent high grade non-Hodgkin's lymphoma and Hodgkin's disease. Yorkshire Regional Lymphoma and Central Lymphoma Groups.

作者信息

Child J A, Simmons A V, Barnard D L, Parapia L, Morgan M, Grace R J, Fletcher J, Parker D, Norfolk D R, Stone J

机构信息

General Infirmary, Leeds, U.K.

出版信息

Hematol Oncol. 1991 Jul-Oct;9(4-5):235-44. doi: 10.1002/hon.2900090409.

Abstract

Fifty-seven patients, initially diagnosed as having advanced high grade non-Hodgkin's lymphoma (NHL) or Hodgkin's disease (HD) refractory to first-line treatment or in relapse, were treated with ifosfamide 6 g/m2, infused over 48 h, followed by mitoxantrone 12 mg/m2. The regimen repeated at three-weekly intervals. Of 33 patients with NHL evaluable for response, 10 (30 per cent) achieved complete remission and six partial remission, giving an overall response rate of 48 per cent. Two patients subsequently went on to bone marrow transplant (BMT)--one allogeneic and the other autologous. Of 18 patients with HD evaluable for response, seven (39 per cent) achieved complete remission and six partial remission, giving an overall response rate of 72 per cent. Two of this group also went on to BMT (both autografts). The principal toxicity was neutropenia, though central nervous system changes were observed in 10 patients. The possibility of increasing the safety of the regimen by increasing the time of infusion to 72 h is discussed. Given the need to offer alternative treatment to patients in these categories, this combination (I-M) is of value in relapsed patients, especially where options are limited because of previous multi-drug treatment. Remissions may not be prolonged but allow the effective application of additional intensive treatment including bone marrow transplantation.

摘要

57例最初被诊断为晚期高级别非霍奇金淋巴瘤(NHL)或霍奇金病(HD)且对一线治疗难治或复发的患者,接受了6 g/m²的异环磷酰胺治疗,在48小时内输注完毕,随后给予12 mg/m²的米托蒽醌。该方案每三周重复一次。在33例可评估疗效的NHL患者中,10例(30%)实现完全缓解,6例部分缓解,总缓解率为48%。2例患者随后接受了骨髓移植(BMT)——1例为异体移植,另1例为自体移植。在18例可评估疗效的HD患者中,7例(39%)实现完全缓解,6例部分缓解,总缓解率为72%。该组中有2例也接受了BMT(均为自体移植)。主要毒性为中性粒细胞减少,不过有10例患者出现了中枢神经系统改变。讨论了将输注时间延长至72小时以提高该方案安全性的可能性。鉴于需要为这类患者提供替代治疗,这种联合方案(I-M)对复发患者有价值,特别是在因先前多药治疗而选择有限的情况下。缓解期可能不会延长,但可有效应用包括骨髓移植在内的其他强化治疗。

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