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Dose-intensified treatment of diffuse large B-cell lymphomas

机译:弥漫性大B细胞淋巴瘤的剂量加强治疗

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About 50% of all patients treated with CHOP (cyclophosphamide, doxorubicin, vincristine and prednisone) achieve complete remission, and about one third experience longterm disease-free survival and cure. Attempts to improve results by modifications of CHOP using escalated doses, additional drugs or the alternative use of putatively non-cross resistant chemotherapy regimens failed in randomised trials. With the availability of granulocyte colony stimulating factor (G-CSF) and the tool of autologous stem-cell support, dose escalation, dose densification (by interval reduction) or combinations thereofwere pursued to increase dose intensity. While dose escalation strategies including high-dose approaches necessitating stem cell support have not yet unequivocally been demonstrated to be superior to a baseline CHOP-21, dose dense (bi-weekly) modifications improved the outcome of young and elderly patients with aggressive lymphomas compared to baseline CHOP-21. Major goals in the rituximab era are the identification of the ideal chemotherapy partner for rituximab and the determination of the role of intensified rituximab within such approaches.
机译:接受CHOP治疗的所有患者(环磷酰胺,阿霉素,长春新碱和泼尼松)中约有50%完全缓解,约三分之一的患者长期无病生存和治愈。在随机试验中,尝试通过增加剂量,使用其他药物或替代使用非交叉耐药化疗方案来改变CHOP来改善结果。随着粒细胞集落刺激因子(G-CSF)的可用性和自体干细胞支持的工具,寻求剂量递增,剂量致密化(通过间隔减少)或其组合以增加剂量强度。虽然尚未明确证实包括高剂量方法在内需要干细胞支持的剂量递增策略优于基线CHOP-21,但与(相比)每两周一次的剂量密集修改改善了患有侵袭性淋巴瘤的年轻和老年患者的预后基线CHOP-21。利妥昔单抗时代的主要目标是确定利妥昔单抗的理想化学疗法伴侣,并确定这种方法中强化的利妥昔单抗的作用。

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