...
首页> 外文期刊>Brazilian Journal of Medical and Biological Research >A third generation regimen VACOP-B with or without adjuvant radiotherapy for aggressive localized non-Hodgkin's lymphoma: report from the Italian Non-Hodgkin's Lymphoma Co-operative Study Group
【24h】

A third generation regimen VACOP-B with or without adjuvant radiotherapy for aggressive localized non-Hodgkin's lymphoma: report from the Italian Non-Hodgkin's Lymphoma Co-operative Study Group

机译:第三代方案VACOP-B伴或不伴辅助放疗,用于侵袭性局灶性非霍奇金淋巴瘤:意大利非霍奇金淋巴瘤合作研究小组的报告

获取原文
           

摘要

The objective of this multicenter prospective study was to determine the clinical efficacy and toxicity of a polychemotherapeutic third generation regimen, VACOP-B, with or without radiotherapy as front-line therapy in aggressive localized non-Hodgkin's lymphoma. Ninety-three adult patients (47 males and 46 females, median age 45 years) with aggressive localized non-Hodgkin's lymphoma, 43 in stage I and 50 in stage II (non-bulky), were included in the study. Stage I patients received VACOP-B for 6 weeks plus involved field radiotherapy and stage II patients received 12 weeks VACOP-B plus involved field radiotherapy on residual masses. Eighty-six (92.5%) achieved complete remission and 4 (4.3%) partial remission. Three patients (3.2%) were primarily resistant. Ten-year probability of survival, progression-free survival and disease-free survival were 87.3, 79.9 and 83.9%, respectively. Eighty-four patients are surviving at a median observation time of 57 months (range: 6-126). Statistical analysis showed no difference between stages I and II in terms of response, ten-year probability of survival, progression-free survival or disease-free survival. Side effects and toxicity were negligible and were similar in the two patient groups. The results of this prospective study suggest that 6 weeks of VACOP-B treatment plus radiotherapy may be the therapy of choice in stage I aggressive non-Hodgkin's lymphoma. Twelve weeks of VACOP-B treatment with or without radiotherapy was shown to be effective and feasible for stage II. These observations need to be confirmed by a phase III study comparing first and third generation protocols in stage I-II aggressive non-Hodgkin's lymphoma.
机译:这项多中心前瞻性研究的目的是确定在有局限性非霍奇金淋巴瘤中采用或不采用放疗作为一线治疗的多药治疗第三代方案VACOP-B的临床疗效和毒性。该研究纳入了93例侵袭性局灶性非霍奇金淋巴瘤的成年患者(男47例,女46例,中位年龄为45岁),I期为43例,II期为50例(非大块)。 I期患者接受VACOP-B治疗6周,并进行了野外放疗; II期患者接受了12周VACOP-B治疗,并进行了野外放疗。百分之八十六(92.5%)的学生获得了完全缓解,部分(4%)(4.3%)获得了缓解。三名患者(3.2%)主要耐药。十年生存率,无进展生存率和无疾病生存率分别为87.3%,79.9和83.9%。 84名患者的中位观察时间为57个月(范围:6-126)。统计分析表明,I,II期在反应,十年生存率,无进展生存期或无疾病生存率方面无差异。副作用和毒性可忽略不计,在两个患者组中相似。这项前瞻性研究的结果表明,VACOP-B治疗加放射治疗6周可能是I期侵袭性非霍奇金淋巴瘤的首选治疗方法。十二周的VACOP-B治疗(有或没有放疗)被证明对II期有效且可行。这些观察结果需要通过一项III期研究来证实,该研究比较了I-II期侵袭性非霍奇金淋巴瘤的第一代和第三代方案。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号