首页> 美国卫生研究院文献>Neuro-Oncology >AT-56TREATMENT OF LARGE LOW-GRADE OLIGODENDROGLIAL TUMORS WITH UPFRONT PROCARBAZINE LOMUSTINE AND VINCRISTINE CHEMOTHERAPY WITH LONG FOLLOW-UP: A RETROSPECTIVE COHORT STUDY WITH GROWTH KINETICS
【2h】

AT-56TREATMENT OF LARGE LOW-GRADE OLIGODENDROGLIAL TUMORS WITH UPFRONT PROCARBAZINE LOMUSTINE AND VINCRISTINE CHEMOTHERAPY WITH LONG FOLLOW-UP: A RETROSPECTIVE COHORT STUDY WITH GROWTH KINETICS

机译:普法卡巴嗪洛莫司汀和长春新碱长程随访对AT-56大低级少突胶质瘤的治疗:生长动力学的回顾性队列研究

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

PURPOSE: We treated patients with newly diagnosed and large low-grade oligodendroglial tumors with upfront procarbazine, lomustine (CCNU) and vincristine (PCV) in our institution in order to delay RT. We now report long term follow-up on a cohort of patients treated between 1998 and 2006. METHODS: Patients were treated with PCV in cycles of 6 weeks, for a maximum of 6 cycles. Central pathology review, genotyping on 1p/19q loss and immunohistochemistry on the IDH1 mutational status and MIB-1 labeling was performed. The response to treatment was defined according to the RANO criteria; in addition change over time of mean tumor diameters (growth kinetics) was calculated. RESULTS: Thirty-two patients were treated, 18 of which were diagnosed with 1p/19q co-deleted tumors. Median follow-up duration was 8 years. The median overall survival (OS) was 120 months and the median progression-free survival (PFS) was 46 months. Growth kinetics showed an ongoing decrease of the mean tumor diameter after completion of chemotherapy, during a median time of 35 months (range 5-136 months), but an increase of the mean tumor diameter did not herald progression as detected by RANO criteria. 1p/19q co-deletion was associated with a significant increase in OS (median OS 83 months versus not reached for codeleted tumors; p = 0.003)) and PFS (median PFS 35 months versus 67 months for codeleted tumors; p = 0.024). Patients with combined 1p/19q loss had a 10 year PFS of 34% and the radiotherapy in these patients was postponed for a median period of more than 6 years. CONCLUSION: This long-term follow-up study indicates that upfront PCV chemotherapy is associated with long PFS and OS and delays radiotherapy for a considerable period of time in patients with low-grade oligodendroglial tumors, in particular with combined 1p/19q loss.
机译:目的:我们在我们的机构中​​用前卡巴嗪,洛莫司汀(CCNU)和长春新碱(PCV)治疗了新诊断并患有大型低度少突胶质细胞瘤的患者,以延迟放疗。现在,我们报告了1998年至2006年间接受治疗的一组患者的长期随访。方法:对患者进行PCV治疗,周期为6周,最多6个周期。进行中央病理学检查,1p / 19q丢失的基因分型以及IDH1突变状态和MIB-1标记的免疫组化。根据RANO标准定义对治疗的反应;此外,还计算了平均肿瘤直径(生长动力学)随时间的变化。结果:治疗了32例患者,其中18例被诊断患有1p / 19q共缺失的肿瘤。中位随访时间为8年。中位总生存期(OS)为120个月,中位无进展生存期(PFS)为46个月。生长动力学显示,在完成化疗后,平均肿瘤直径在35个月(范围5-136个月)中持续下降,但是平均肿瘤直径的增加并未预示着RANO标准的进展。 1p / 19q共删除与OS(中位OS的83个月相比,未编码的肿瘤未达到; P = 0.003))和PFS(中位PFS 35个月而对已编码的肿瘤,67个月; P = 0.024)显着增加有关。合并1p / 19q损失的患者的10年PFS为34%,这些患者的放疗被推迟了6年以上。结论:这项长期的随访研究表明,对于低度少突胶质神经胶质瘤患者,特别是合并1p / 19q丢失的患者,前期PCV化疗与长PFS和OS相关,并在相当长的一段时间内延迟放疗。

著录项

相似文献

  • 外文文献
  • 中文文献
代理获取

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