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PET-adapted treatment for newly diagnosed advanced Hodgkin lymphoma (AHL2011): a randomised, multicentre, non-inferiority, phase 3 study

机译:宠物适应治疗新诊断的晚期霍奇金淋巴瘤(AHL2011):随机,多期中心,非劣等,第3期研究

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Background Increased-dose bleomycin, etoposide, doxorubicin, cyclophosphamide, vincristine, procarbazine, and prednisone (BEACOPP(escalated)) improves progression-free survival in patients with advanced Hodgkin lymphoma compared with doxorubicin, bleomycin, vinblastine, and dacarbazine (ABVD), but is associated with increased risks of haematological toxicity, secondary myelodysplasia or leukaemia, and infertility. We investigated whether PET monitoring during treatment could allow dose de-escalation by switching regimen (BEACOPP(escalated) to ABVD) in early responders without loss of disease control compared with standard treatment without PET monitoring.
机译:背景技术与多柔枯蛋白,博莱霉素,长春毒素和达卡尿嘧啶(ABVD)相比,增加剂量博来霉素,依托磷脂,转基因磷,环磷酰胺,环磷酰胺(Beacopp(升级))改善了霍奇金淋巴瘤患者的无进展生存期,但是 与血液学毒性,继发性髓细胞普及或白血病的风险增加有关,以及不孕症。 我们调查了治疗期间的PET监测是否可以通过在早期响应者中切换方案(BEACPP(升级)到ABVD)在没有宠物监测的标准治疗的情况下在早期响应者中切换治疗方案(BEACPP(升级)到ABVD)。

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