首页> 美国卫生研究院文献>Neuro-oncology Advances >ACT-09 RETROSPECTIVE INVESTIGATION ABOUT STATUS AND RESULT OF ADMINISTRATION OF BEVACIZUMAB FOR MALIGNANT GLIOMAS IN THE REAL WORLD
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ACT-09 RETROSPECTIVE INVESTIGATION ABOUT STATUS AND RESULT OF ADMINISTRATION OF BEVACIZUMAB FOR MALIGNANT GLIOMAS IN THE REAL WORLD

机译:ACT-09回顾性研究现实世界中恶性胶质瘤的贝伐单抗的管理状况和结果

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摘要

6 years have passed after approval of Bevacizumab for malignant gliomas in Japan, we analyzed the application and the results in our institution. Subjects were 56 patients who were histologically diagnosed as malignant gliomas. Bevacizumab was used in 41 patients among them. In 14 patients, Bevacizumab was introduced after initial therapy. The resection rates were below partial resection in 11 of the 14 patients. In 12 patients, administrations were finished and the average use was 7.6 times. The reason was PD in 6, and side effect in 4. Eight patients died, the average OS of those who died was 9.9 months, the average PFS after Bevacizumab was 5.4 months, and the average time from discontinuation to death was 2.1 months. In 27 patients used at the time of recurrence, the initial excision rate tended to be higher than in the former cases. In 22 patients the administrations were finished and the average use was 11.1 times. The reason was PD in 17, and side effect in 4. Twenty patients have died, the average OS of those who died was 22.3 months, the average PFS after Bevacizumab was 7.1 months, and the average time from discontinuation to death was 2.6 months. In 12 of 15 unused patients subtotal or total resections were achieved. From results, when it is difficult to control by surgery or TMZ, Bevacizumab is used in most patients, and considering the nature of tumor, it can be said that all patients will be considered for use sometime. However, PFS after introduction is not good and the prognosis after discontinuation is poor. It is necessary to conduct initial treatment that can delay introduction, to provide care that does not lead to discontinuation due to side effects, and to examine what treatment is possible at the time of exacerbation.
机译:在日本贝伐单抗用于恶性神经胶质瘤的批准已经过去了6年,我们分析了该机构的应用和结果。受试者为56例经组织学诊断为恶性神经胶质瘤的患者。其中41例患者使用了贝伐单抗。在14例患者中,初始治疗后引入了贝伐单抗。 14例患者中有11例的切除率低于部分切除率。 12例患者完成了给药,平均使用量是7.6倍。原因是PD发生在6位,副作用发生在4位。死亡8例,死亡者的平均OS为9.9个月,贝伐单抗治疗后的平均PFS为5.4个月,从停药到死亡的平均时间为2.1个月。在复发时使用的27例患者中,初始切除率往往高于以前的病例。在22例患者中,用药结束,平均使用量为11.1倍。原因是17例PD,4例副作用。死亡20例,死亡者的平均OS为22.3个月,贝伐单抗治疗后的平均PFS为7.1个月,从停药到死亡的平均时间为2.6个月。 15例未使用的患者中有12例全部或全部切除。从结果来看,当难以通过手术或TMZ进行控制时,贝伐单抗在大多数患者中使用,并且考虑到肿瘤的性质,可以说所有患者均会考虑使用。但是,引入后的PFS不好,停药后的预后很差。有必要进行可能延迟引入的初始治疗,以提供不会因副作用而导致停药的护理,并检查在恶化时可以采取何种治疗措施。

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