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MINE方案作为复发难治性霍奇金淋巴瘤的强化挽救化疗方案。

The MINE regimen as intensive salvage chemotherapy for relapsed and refractory Hodgkin's disease.

作者信息

Fermé C, Bastion Y, Lepage E, Berger F, Brice P, Morel P, Gabarre J, Nédellec G, Reman O, Chéron N

机构信息

Groupe d'Etudes des Lymphomes de l'Adulte, Hôpital Saint-Louis, Paris, France.

出版信息

Ann Oncol. 1995 Jul;6(6):543-9. doi: 10.1093/oxfordjournals.annonc.a059242.

Abstract

BACKGROUND

Relapsed or refractory Hodgkin's disease (HD) patients were treated with an intensive salvage regimen (MINE) prior to high-dose therapy (HDT) with hematopoietic stem cell support.

PATIENTS AND METHODS

One hundred HD patients who either failed to respond to a front-line chemotherapy regimen (induction failure, n = 41) or relapsed (untreated relapse, n = 54; resistant relapse, n = 5) were treated with the MINE regimen. Each course of MINE comprised mitoguazone 500 mg/m2 on days 1 and 5, ifosfamide 1500 mg/m2/d from day 1 to day 5, vinorelbine (Navelbine) 15 mg/m2 on days 1 and 5, and etoposide 150 mg/m2/d from day 1 to day 3. At least two courses were given at 4-week intervals. Then, 72 patients received HDT followed by hematopoietic stem cell support.

RESULTS

After MINE salvage, 34 patients achieved a complete response (CR) and 39 a partial response, yielding an overall response rate of 75%. Patients with untreated relapse had a 92.5% response rate and those with resistant relapse or induction failure a 53% response rate. A total of 58 patients reached a CR at the end of all treatments; 12 of them relapsed. Sixty-six patients were alive with a median follow-up of 26 months, including 46 patients in CR. The 2-year survival rate for the entire group was 59%. By univariate analysis, patients with an interval between their last treatment and salvage longer than 12 months, untreated relapse, or good performance status at salvage are shown to have longer survivals. The main toxic effects were neutropenia, thrombocytopenia, and infectious episodes. Three patients died of MINE-related complications and three after HDT.

CONCLUSION

Given early in the course of progressive HD, the MINE regimen reduced tumor burden in a high proportion of patients with relapsed or refractory disease. Responding patients further intensified with HDT have a better outcome than those who have not responded to salvage treatment.

摘要

背景

复发或难治性霍奇金淋巴瘤(HD)患者在接受造血干细胞支持的大剂量治疗(HDT)之前,先接受了强化挽救方案(MINE)治疗。

患者与方法

100例HD患者,其中对一线化疗方案无反应者(诱导失败,n = 41)或复发者(未治疗的复发,n = 54;耐药复发,n = 5)接受了MINE方案治疗。MINE的每个疗程包括在第1天和第5天给予丙脒腙500mg/m²,从第1天至第5天给予异环磷酰胺1500mg/m²/天,在第1天和第5天给予长春瑞滨(诺维本)15mg/m²,从第1天至第3天给予依托泊苷150mg/m²/天。至少每4周给予两个疗程。然后,72例患者接受了HDT并随后接受造血干细胞支持。

结果

经过MINE挽救治疗后,34例患者达到完全缓解(CR),39例患者达到部分缓解,总缓解率为75%。未治疗的复发患者缓解率为92.5%,耐药复发或诱导失败患者缓解率为53%。在所有治疗结束时,共有58例患者达到CR;其中12例复发。66例患者存活,中位随访时间为26个月,包括46例处于CR的患者。整个组的2年生存率为59%。单因素分析显示,最后一次治疗与挽救治疗之间的间隔超过12个月、未治疗的复发或挽救治疗时体能状态良好的患者生存期较长。主要毒副作用为中性粒细胞减少、血小板减少和感染性发作。3例患者死于与MINE相关的并发症,3例患者在HDT后死亡。

结论

在进行性HD病程早期给予MINE方案,可使很大一部分复发或难治性疾病患者的肿瘤负荷降低。对挽救治疗有反应的患者进一步强化HDT后的结局优于对挽救治疗无反应的患者。

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