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首页> 外文期刊>Hematological oncology >A salvage chemotherapy of R-P-IMVP16/CBDCA consisting of rituximab, methylprednisolone, ifosfamide, methotrexate, etoposide, and carboplatin for patients with diffuse large B cell lymphoma who had previously received R-CHOP therapy as first-line chemotherapy
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A salvage chemotherapy of R-P-IMVP16/CBDCA consisting of rituximab, methylprednisolone, ifosfamide, methotrexate, etoposide, and carboplatin for patients with diffuse large B cell lymphoma who had previously received R-CHOP therapy as first-line chemotherapy

机译:R-P-IMVP16 / CBDCA的救生化疗由Rituximab,甲基己酮,Ifosfamide,甲氨蝶呤,依托泊苷和Carboplatin组成,用于弥漫性大B细胞淋巴瘤患者,患者作为一线化疗的R-Chec疗法

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We have reported the efficacy of the salvage chemotherapy P-IMVP16/CBDCA for patients with diffuse large B cell lymphoma (DLBCL) who had previously received CHOP before the availability of rituximab (R). Here, we confirmed the efficacy of R combined with P-IMVP16/CBDCA as a salvage chemotherapy for patients with DLBCL, who had previously received R-CHOP. We retrospectively analysed 59 patients with relapse or refractory DLBCL (38 male patients and 21 female patients) presenting between June 2004 and June 2013. The patients received R 375mg/m(2) on day 1, methylprednisolone 1000mg/body for 3days (from day 3 to day 5), ifosfamide 1000mg/m(2) for 5days (from day 3 to day 7), methotrexate 30mg/m(2) on day 5 and day 12, etoposide 80mg/m(2) for 3days (from day 3 to day 5), and carboplatin 300mg/m(2) on day 3 every 21days. Patients aged 70years or older were given 75% of the standard dose. The overall response rate (complete response+partial response) was 64.4%. The 2-year overall survival rate was 55.3%. The 2-year progression free survival rate was 34.7%. The 2-year overall survival rate was 61.5% for the relapse patients, and 15.6% for the refractory patients (p<0.0001). One patient died because of sepsis related to the treatment regimen. Non-hematological adverse effects were mild and tolerable. The R-P-IMVP-16/CBDCA regimen displayed a significant activity in relapsed DLBCL, with acceptable toxicity, and should be considered a candidate for salvage chemotherapy. Copyright (c) 2016 John Wiley & Sons, Ltd.
机译:我们已经报道了拯救化疗P-IMVP16 / CBDCA对弥漫性大B细胞淋巴瘤(DLBCL)的患者的疗效,该患者先前在RITUXIMAB(R)的可用性之前已经接受过切碎的。在这里,我们确认R合并P-IMVP16 / CBDCA作为患有先前接受R-Chec的患者的患者的救助化疗。我们回顾性分析了2004年6月至2013年6月在2004年6月至6月期间的59例复发或难治性DLBCL(38名男性患者和21例女性患者)。患者在第1天,甲基丙酮酮1000mg /体育患者进行3天(从一天开始) 3至第5天),IFOSFamide 1000mg / m(2)为50mg /第7天(从第3天),第5天和第12天的甲氨蝶呤30mg / m(2),依托泊苷80mg / m(2)为3天(从一天开始) 3至第5天),每21天每天300mg / m(2)卡铂300mg / m(2)。 70岁或以上的患者获得75%的标准剂量。整体响应率(完全响应+部分反应)为64.4%。 2年的总生存率为55.3%。 2年的进展免费生存率为34.7%。复发患者的2年整体存活率为61.5%,难治患者的15.6%(P <0.0001)。一名患者因与治疗方案有关的败血症而死亡。非血液不良反应温和可耐磨。 R-P-IMVP-16 / CBDCA方案在复发的DLBCL中显示出显着的活性,具有可接受的毒性,并且应该被认为是救助化疗的候选者。版权所有(c)2016 John Wiley&Sons,Ltd。

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