具有心血管危险因素的经典霍奇金淋巴瘤患者的PBVD治疗方案(聚乙二醇化脂质体阿霉素、博来霉素、长春新碱、达卡巴嗪):一项回顾性研究

IF 2.2 4区 医学 Q3 HEMATOLOGY
Jia Jin, Dan-Dan Meng, Yu Wen, Qun-Ling Zhang, Fang-Fang Lv, Guang-Liang Chen, Xue-Jun Ma, Bao-Hua Yu, Sheng-Jian Zhang, Chang Liu, Zu-Guang Xia
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引用次数: 0

摘要

本回顾性研究旨在评价PBVD(聚乙二醇化脂质体多柔比星[PLD]、博来霉素、长春碱和达卡巴嗪)一线治疗伴有心血管危险因素的经典霍奇金淋巴瘤(cHL)患者的疗效和安全性。总体而言,84例患者(53例为I-II期,31例为III-IV期)接受了PBVD。I-II期PLD治疗的中位持续时间为16周(四分位数间距[IQR]: 8-24), III-IV期为24周(IQR: 12-24)。其中56例(66.7%)接受放疗,其中I-II期45例,III-IV期11例。74例(88.1%)患者获得完全缓解。在49.7个月的中位随访中,2年和5年无进展生存率均为83.2%,总生存率为98.7%和94.9%。不良事件发生率为73.8%,其中心脏事件发生率为7.1%。未观察到与治疗相关的死亡。该方法在该人群中显示出良好的收益-风险比。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
PBVD regimen (pegylated liposomal doxorubicin, bleomycin, vincristine, dacarbazine) in classical Hodgkin lymphoma patients with cardiovascular risk factors: a retrospective study.

This retrospective study aimed to evaluate the efficacy and safety of PBVD (pegylated liposomal doxorubicin [PLD], bleomycin, vinblastine, and dacarbazine) in the first-line treatment of classical Hodgkin lymphoma (cHL) patients with cardiovascular risk factors. Overall, 84 patients (53 had stage I-II and 31 had stage III-IV disease) received PBVD. The median PLD treatment duration was 16 weeks (interquartile range [IQR]: 8-24) for stage I-II and 24 weeks (IQR: 12-24) for stage III-IV. Among them, 56 (66.7%) received radiotherapy (45 with stage I-II and 11 with stage III-IV disease). Seventy-four (88.1%) patients achieved complete response. At a median follow-up of 49.7 months, 2- and 5-year progression-free survival were both 83.2%, and overall survival was 98.7% and 94.9%. Adverse events occurred in 73.8% of patients, including 7.1% cardiac events. No treatment-related deaths were observed. This approach showed a favorable benefit-to-risk profile in this population.

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来源期刊
Leukemia & Lymphoma
Leukemia & Lymphoma 医学-血液学
CiteScore
4.10
自引率
3.80%
发文量
384
审稿时长
1.8 months
期刊介绍: Leukemia & Lymphoma in its fourth decade continues to provide an international forum for publication of high quality clinical, translational, and basic science research, and original observations relating to all aspects of hematological malignancies. The scope ranges from clinical and clinico-pathological investigations to fundamental research in disease biology, mechanisms of action of novel agents, development of combination chemotherapy, pharmacology and pharmacogenomics as well as ethics and epidemiology. Submissions of unique clinical observations or confirmatory studies are considered and published as Letters to the Editor
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