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晚期霍奇金淋巴瘤患者接受四个周期的博来霉素、依托泊苷、多柔比星、环磷酰胺、长春新碱、泼尼松、丙卡巴肼(BEACOPP)强化方案,随后再接受四个周期的基线剂量BEACOPP方案的十年经验:一项单中心回顾性研究。

Ten years' experience with four cycles of bleomycin, etoposide, doxorubicin, cyclophosphamide, vincristine, prednisone, procarbazine (BEACOPP)-escalated followed by four cycles of baseline-dose BEACOPP in patients with advanced stage Hodgkin lymphoma: a single-center, retrospective study.

作者信息

Belada David, Štěpánková Pavla, Sýkorová Alice, Žák Pavel, Smolej Lukáš

机构信息

4th Department of Internal Medicine - Hematology, Charles University Hospital and Faculty of Medicine , Hradec Králové , Czech Republic.

出版信息

Leuk Lymphoma. 2015 Jul;56(7):2013-8. doi: 10.3109/10428194.2014.975804. Epub 2015 Feb 10.

DOI:10.3109/10428194.2014.975804
PMID:25330440
Abstract

The HD-9 trial showed that eight cycles of BEACOPP (bleomycin, etoposide, doxorubicin, cyclophosphamide, vincristine, prednisone, procarbazine)-escalated led to significant improvements in response rate, progression-free survival and overall survival over COPP/ABVD (cyclophosphamide, vincristine, prednisone, procarbazine/doxorubicin, bleomycin, vinblastine, dacarbazine) therapy. This monocentric retrospective study was performed to evaluate 10 years of experience with four cycles of BEACOPP-escalated and four cycles of BEACOPP-baseline outside of clinical trials. The outcomes were assessed in 78 patients with newly diagnosed advanced stage Hodgkin lymphoma. A complete response after chemotherapy ± radiotherapy was achieved in 75 patients (96%). At the median follow-up of 74 months, the actuarial 5- and 10-year freedom from treatment failure (FFTF) rates were 91% and 89%, and actuarial 5- and 10-year overall survival rates for the entire group were 93% and 90%, respectively. These results suggest that the combination of escalated and baseline BEACOPP chemotherapy is feasible in routine practice with good efficacy and acceptable toxicity.

摘要

HD - 9试验表明,与COPP/ABVD(环磷酰胺、长春新碱、泼尼松、丙卡巴肼/多柔比星、博来霉素、长春花碱、达卡巴嗪)疗法相比,8个周期的强化BEACOPP(博来霉素、依托泊苷、多柔比星、环磷酰胺、长春新碱、泼尼松、丙卡巴肼)方案可显著提高缓解率、无进展生存期和总生存期。本单中心回顾性研究旨在评估在临床试验之外应用4个周期强化BEACOPP方案和4个周期基础BEACOPP方案的10年经验。对78例新诊断的晚期霍奇金淋巴瘤患者的治疗结果进行了评估。75例患者(96%)在化疗±放疗后获得完全缓解。在中位随访74个月时,精算得出的5年和10年无治疗失败生存率分别为91%和89%,整个组的精算5年和10年总生存率分别为93%和90%。这些结果表明,强化和基础BEACOPP化疗联合方案在常规实践中是可行的,疗效良好且毒性可接受。

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