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Novel combination of epirubicin, bleomycin, vinblastine and prednisone (EBVP II) before radical radiotherapy in localized stages (I-IIIA) of Hodgkin's disease. Early results in 100 consecutive patients. Pierre-et-Marie-Curie Group.在局限性(I-IIIA期)霍奇金淋巴瘤患者根治性放疗前应用表柔比星、博来霉素、长春碱和泼尼松的新型联合方案(EBVP II)。100例连续患者的早期结果。皮埃尔和玛丽居里研究小组
J Cancer Res Clin Oncol. 1991;117(4):377-80. doi: 10.1007/BF01630723.
2
Comparison of first-line chemotherapy including escalated BEACOPP versus chemotherapy including ABVD for people with early unfavourable or advanced stage Hodgkin lymphoma.对早期预后不良或晚期霍奇金淋巴瘤患者,比较包括强化BEACOPP方案的一线化疗与包括ABVD方案的化疗。
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3
Optimisation of chemotherapy and radiotherapy for untreated Hodgkin lymphoma patients with respect to second malignant neoplasms, overall and progression-free survival: individual participant data analysis.未治疗的霍奇金淋巴瘤患者化疗和放疗在第二原发性恶性肿瘤、总生存期和无进展生存期方面的优化:个体参与者数据分析
Cochrane Database Syst Rev. 2017 Sep 13;9(9):CD008814. doi: 10.1002/14651858.CD008814.pub2.
4
[New combination of epirubicine, bleomycin, vinblastine and prednisone (EBVP II) before radiotherapy in localized stages of Hodgkin's disease. Phase II trial in 50 patients].
Bull Cancer. 1988;75(8):789-94.
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[The combination of epirubicin, bleomycin, vinblastine and prednisone (EBVP) before radiotherapy in localized stages of Hodgkin's disease. Phase II trials].
Bull Cancer. 1987;74(2):151-7.
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Preliminary results of the EORTC-GPMC controlled clinical trial H7 in early-stage Hodgkin's disease. EORTC Lymphoma Cooperative Group. Groupe Pierre-et-Marie-Curie.欧洲癌症研究与治疗组织-皮埃尔和玛丽·居里肿瘤中心关于早期霍奇金淋巴瘤的H7对照临床试验的初步结果。欧洲癌症研究与治疗组织淋巴瘤协作组。皮埃尔和玛丽·居里肿瘤中心。
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Positron emission tomography-adapted therapy for first-line treatment in individuals with Hodgkin lymphoma.正电子发射断层扫描适配疗法用于霍奇金淋巴瘤患者的一线治疗
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Comparison of chemotherapy including escalated BEACOPP versus chemotherapy including ABVD for patients with early unfavourable or advanced stage Hodgkin lymphoma.早期预后不良或晚期霍奇金淋巴瘤患者中,强化BEACOPP化疗方案与ABVD化疗方案的比较。
Cochrane Database Syst Rev. 2011 Aug 10(8):CD007941. doi: 10.1002/14651858.CD007941.pub2.

本文引用的文献

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Extended versus involved fields irradiation combined with MOPP chemotherapy in early clinical stages of Hodgkin's disease.霍奇金病早期临床阶段扩大野照射与受累野照射联合MOPP化疗的比较
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Predictive value of the early response to chemotherapy in high-risk stages II and III Hodgkin's disease.高危II期和III期霍奇金淋巴瘤化疗早期反应的预测价值
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Adriamycin versus epirubicin in advanced soft tissue sarcomas. A randomized phase II/phase III study of the EORTC Soft Tissue and Bone Sarcoma Group.
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The chemotherapy of lymphomas: looking back, moving forward--the Richard and Hinda Rosenthal Foundation award lecture.淋巴瘤的化疗:回顾与展望——理查德和欣达·罗森塔尔基金会奖讲座
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A prospective randomized phase III trial comparing combination chemotherapy with cyclophosphamide, fluorouracil, and either doxorubicin or epirubicin. French Epirubicin Study Group.一项前瞻性随机III期试验,比较环磷酰胺、氟尿嘧啶与多柔比星或表柔比星联合化疗。法国表柔比星研究组。
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6
Influence of dose intensity and density on therapeutic and toxic effects in Hodgkin's disease.剂量强度和密度对霍奇金淋巴瘤治疗效果及毒性反应的影响
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7
Quality of life during and after treatment of Hodgkin's disease.霍奇金淋巴瘤治疗期间及治疗后的生活质量。
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Hodgkin's disease: challenges for the future.霍奇金淋巴瘤:未来的挑战
Cancer Res. 1989 Feb 15;49(4):767-9.
9
[New combination of epirubicine, bleomycin, vinblastine and prednisone (EBVP II) before radiotherapy in localized stages of Hodgkin's disease. Phase II trial in 50 patients].
Bull Cancer. 1988;75(8):789-94.
10
[The combination of epirubicin, bleomycin, vinblastine and prednisone (EBVP) before radiotherapy in localized stages of Hodgkin's disease. Phase II trials].
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在局限性(I-IIIA期)霍奇金淋巴瘤患者根治性放疗前应用表柔比星、博来霉素、长春碱和泼尼松的新型联合方案(EBVP II)。100例连续患者的早期结果。皮埃尔和玛丽居里研究小组

Novel combination of epirubicin, bleomycin, vinblastine and prednisone (EBVP II) before radical radiotherapy in localized stages (I-IIIA) of Hodgkin's disease. Early results in 100 consecutive patients. Pierre-et-Marie-Curie Group.

作者信息

Hoerni B, Orgerie M B, Eghbali H, Blanc C M, David B, Rojouan J, Zittoun R

机构信息

Fondation Bergonié, Bordeaux, France.

出版信息

J Cancer Res Clin Oncol. 1991;117(4):377-80. doi: 10.1007/BF01630723.

DOI:10.1007/BF01630723
PMID:1712359
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12200917/
Abstract

A novel combination of epirubicin, bleomycin, vinblastine and prednisone (EBVP II) was scheduled to reduce the toxicity of chemotherapy and to improve its application in treatment of Hodgkin's disease. This combination followed a previous regimen given every 15 days (EBVP I) by the same cooperative group. EPVP II is given every 21 days with increased dosage and increased intensity of epirubicin. This regimen was given to 100 consecutive patients with favourable or unfavourable limited-stage disease (clinical stages I-IIIA) excluding very favourable stages I and II and stages IIIB and IV. Such patients first received three injections of EBVP II and were then radically irradiated; those with unfavourable prognosis factors received three subsequent injections of EBVP II. The present analysis reports the early results of such treatment and considers particularly toxicity and the obtention of complete remission, which is pre-eminent for a cure. EBVP II was given in full dosage in 99% of the primary set of three injections. The main toxicity was alopecia and to a lesser degree nausea and vomiting and veinitis. Complete remission was obtained in 76 patients before radiotherapy and in 20 others after radiotherapy. With a median follow-up of 30 months 1 patient died from Hodgkin's disease, 9 are alive after relapse and 90 with no evidence of disease. This treatment appears to be as efficient as previous chemotherapy, well tolerated and particularly easy to give. It deserves further comparison with other proved regimens taking into consideration the survival and quality of life of patients.

摘要

表柔比星、博来霉素、长春碱和泼尼松的新型联合方案(EBVP II)旨在降低化疗毒性,并改善其在霍奇金病治疗中的应用。该联合方案是同一协作组在之前每15天给药一次的方案(EBVP I)基础上制定的。EBVP II每21天给药一次,表柔比星剂量增加且强度加大。该方案用于连续100例具有有利或不利局限期疾病(临床I-IIIA期)的患者,不包括非常有利的I期和II期以及IIIB期和IV期。此类患者首先接受三次EBVP II注射,然后进行根治性放疗;预后不良因素的患者随后再接受三次EBVP II注射。本分析报告了这种治疗的早期结果,并特别考虑了毒性和完全缓解的情况,完全缓解对于治愈至关重要。在最初的三次注射中,99%的患者接受了全剂量的EBVP II。主要毒性为脱发,恶心、呕吐和静脉炎程度较轻。放疗前76例患者获得完全缓解,放疗后另外20例患者获得完全缓解。中位随访30个月,1例患者死于霍奇金病,9例复发后存活,90例无疾病证据。这种治疗似乎与之前的化疗同样有效,耐受性良好,且给药特别容易。考虑到患者的生存率和生活质量,它值得与其他已证实的方案进行进一步比较。