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ChlVPP方案治疗霍奇金淋巴瘤:960例患者的经验。国际ChlVPP治疗组

ChlVPP therapy for Hodgkin's disease: experience of 960 patients. The International ChlVPP Treatment Group.

出版信息

Ann Oncol. 1995 Feb;6(2):167-72.

PMID:7786824
Abstract

BACKGROUND

Combination chemotherapy or combined chemo-radiotherapy is the treatment of choice for patients with advanced stage Hodgkin's disease and for patients failing curative radiotherapy. Increasingly, particularly in Europe, patients with early stage disease with poor prognostic features are also primarily treated with chemotherapy or combined chemo-radiotherapy. We analyzed the experience of 4 research groups which used ChlVPP, with or without radiotherapy, as standard chemotherapy for Hodgkin's disease.

PATIENTS AND METHODS

Patients with Hodgkin's disease were treated with ChlVPP chemotherapy: days 1-14: chlorambucil: 6 mg/m2/day, procarbazine: 100 mg/m2/day, prednisone or prednisolone: 40 mg/day; Days 1, 8: vinblastine: 6 mg/m2/day. The use of radiotherapy varied across research groups, with many, but not all, patients receiving radiotherapy.

RESULTS

A total of 960 patients were treated. 60% were male, 25% were aged 50+, 59% had nodular sclerosis histology. Failure-free survival (time to first occurrence of progression, relapse after response or death from any cause) at 5 years by stage was: Stage I/IIA (231 patients), 75%; I/IIB (152 patients), 62%; IIIA (180 patients), 67%; IIIB/IV (397 patients), 51%. Adverse prognostic factors for all patients included age 50+ and 'B' symptoms. Patients aged 50+ of all stages did especially poorly on ChlVPP therapy. The 34 stage IIIB/IV patients with lymphocyte depleted histology also did poorly.

CONCLUSIONS

These results compare favorably with other reported series. ChlVPP is an appropriate alternative to other chemotherapy regimens for some Hodgkin's disease patients, often with a reduced toxicity profile. Other chemotherapy may be preferred in patients greater than 50 years of age.

摘要

背景

联合化疗或放化疗联合是晚期霍奇金病患者以及根治性放疗失败患者的首选治疗方法。越来越多的,特别是在欧洲,具有不良预后特征的早期疾病患者也主要接受化疗或放化疗联合治疗。我们分析了4个研究组使用ChlVPP(含或不含放疗)作为霍奇金病标准化疗方案的经验。

患者与方法

霍奇金病患者接受ChlVPP化疗:第1 - 14天:苯丁酸氮芥:6 mg/m²/天,丙卡巴肼:100 mg/m²/天,泼尼松或泼尼松龙:40 mg/天;第1、8天:长春花碱:6 mg/m²/天。各研究组放疗的使用情况不同,许多(但并非所有)患者接受了放疗。

结果

共治疗960例患者。60%为男性,25%年龄在50岁以上,59%为结节硬化组织学类型。按分期计算的5年无失败生存率(至首次出现病情进展、缓解后复发或任何原因死亡的时间)为:Ⅰ/ⅡA期(231例患者),75%;Ⅰ/ⅡB期(152例患者),62%;ⅢA期(180例患者),67%;ⅢB/Ⅳ期(397例患者),51%。所有患者的不良预后因素包括年龄50岁以上和“B”症状。所有分期中年龄50岁以上患者接受ChlVPP治疗的效果特别差。34例ⅢB/Ⅳ期淋巴细胞消减组织学类型的患者效果也较差。

结论

这些结果与其他报道的系列研究结果相比具有优势。对于一些霍奇金病患者,ChlVPP是其他化疗方案的合适替代方案,其毒性通常较低。50岁以上患者可能更适合其他化疗方案。

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