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首页> 外文期刊>Medical oncology >Long-term outcome of mesna, ifosfamide, mitoxantrone, etoposide (MINE) regimen as a consolidation in patients with aggressive non-Hodgkin lymphoma responding to CHOP.
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Long-term outcome of mesna, ifosfamide, mitoxantrone, etoposide (MINE) regimen as a consolidation in patients with aggressive non-Hodgkin lymphoma responding to CHOP.

机译:美沙酮,异环磷酰胺,米托蒽醌,依托泊苷(MINE)方案的长期结果可作为对CHOP有反应的侵袭性非霍奇金淋巴瘤患者的巩固治疗。

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摘要

In aggressive non-Hodgkin lymphoma (NHL), CHOP (cyclophosphamide, vincristine, doxorubicin, prednisolone) regimen has been standard for decades, and rituximab has increased response rates and survival in CD20 positive patients, recently. The aim of this prospective trial was to evaluate the long-term efficacy and toxicity of MINE as a consolidation treatment in aggressive NHL patients who had achieved CR or unproven CR after six cycles of CHOP in the first line setting. The primary end-point was disease-free-survival (DFS). Thirty-eight patients were enrolled between February 1992 and May 2000. All of the patients received two cycles of MINE (mesna 1.3 g/m(2), ifosfamide 1.3 g/m(2), etoposide 65 mg/m(2) on days 1-3, and mitoxantrone 12 mg/m(2) on day 1, every 3 weeks) following response to CHOP. Initial bulky disease sites were also applied radiotherapy. Male/female ratio was 1.53(23/15). Median age was 49(30-73). Most of the patients had advanced stage (84.2% for stage >3) and high IPI score (79% for IPI score >2). Sixty percent had diffuse large cell histology. Median follow-up time was 118 months (9-195). Actual mean dose intensity was 88%. There were seven febrile neutropenia episodes. Two patients had grade two neuropathy, one had grade three mucositis and another one had non-neutropenic pneumonia. There was no early toxic death. No serious late toxicity was observed during long-term follow-up. Five- and 10-year DFS rates were both 65.3%. DFS rate in the patients with more than two poor prognostic factors according to IPI score is remarkably high (88%). Five- and 10-year OS was 62.5 and 59%, respectively. MINE regimen seems to be effective as a consolidation regimen, especially, in intermediate/high risk patients and has low early and late toxicities, and it warrants to be evaluated in phase III randomised trials with rituximab in CD20 positive aggressive NHL patients.
机译:在侵袭性非霍奇金淋巴瘤(NHL)中,CHOP(环磷酰胺,长春新碱,阿霉素,泼尼松龙)方案已成为标准方案,数十年来,利妥昔单抗已提高了CD20阳性患者的缓解率和生存率。这项前瞻性试验的目的是评估在一线环境中经过六个周期的CHOP治疗后获得CR或未经证实的CR的积极性NHL患者,MINE作为巩固治疗的长期疗效和毒性。主要终点是无病生存期(DFS)。在1992年2月至2000年5月之间招募了38例患者。所有患者均接受了两个周期的MINE治疗(美沙酮1.3 g / m(2),异环磷酰胺1.3 g / m(2),依托泊苷65 mg / m(2))。第1-3天,并在对CHOP的响应后每3周第1天给予米托蒽醌12 mg / m(2)。最初的大块疾病部位也进行了放射治疗。男女比例为1.53(23/15)。中位数年龄为49(30-73)。大多数患者具有晚期(≥3期为84.2%)和较高的IPI评分(≥2为IPI评分为79%)。 60%的患者有弥漫性大细胞组织学检查。中位随访时间为118个月(9-195)。实际平均剂量强度为88%。有七个发热性中性粒细胞减少症发作。两名患者患有二级神经病变,一名患有三级粘膜炎,另一名患有非中性粒细胞性肺炎。没有早期中毒死亡。长期随访中未观察到严重的后期毒性。五年和十年期DFS率均为65.3%。根据IPI评分,具有两个以上不良预后因素的患者的DFS率极高(88%)。五年和十年OS分别为62.5和59%。 MINE方案似乎可以作为巩固方案,特别是在中/高风险患者中,并且早期和晚期毒性低,并且有必要在CD20阳性侵袭性NHL患者的利妥昔单抗III期随机试验中进行评估。

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