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新诊断的多形性胶质母细胞瘤埃及患者同步放化疗后延长辅助替莫唑胺治疗的疗效与安全性

The efficacy and safety of extended adjuvant temozolomide following concurrent radio-chemotherapy among Egyptian patients with newly diagnosed glioblastoma multiforme.

作者信息

Attia Alia M, Eltybe Hanan A, Sedik Mayada F, Hefni Ahmed Mubarak, Abdelgawad Marwa I, Farrag Ashraf, Essa Abdelhakeem A, El-Barody Mohamed M, Attia Noha M

机构信息

Radiation Oncology Department, South Egypt Cancer Institute, Assiut University Assiut 71515, Egypt.

Department of Medical Oncology and Hematological Malignancies, South Egypt Cancer Institute, Assiut University Assiut 71111, Egypt.

出版信息

Am J Cancer Res. 2022 Jan 15;12(1):355-370. eCollection 2022.

Abstract

Although concurrent radio-chemotherapy and adjuvant temozolomide (TMZ) treatment for 6 cycles has been established as a standard of care for newly diagnosed glioblastoma multiforme (GBM) patients, the recommended duration of adjuvant TMZ remains a matter of debate. Hereby, we aimed to report for the first time our experience from Upper Egypt through comparing survival and toxicity profile between two treatment modalities of adjuvant TMZ (> six cycles versus six cycles) and delineating factors of prognostic significance in Egyptian patients with newly diagnosed GBM treated by radiation therapy with concomitant and adjuvant TMZ. Between June 2016 and February 2018, the medical records of 121 patients were eligible to be retrospectively reviewed to extract the study relevant data. All patients received concurrent radio-chemotherapy, followed by TMZ for 6 cycles in 29 patients (Group 1) and for >6 cycles in 26 patients (Group 2). Patients in Group 1 had a median PFS of 15 months (95% CI: 10.215-19.785), while those in Group 2 had a median PFS of 18 months (95% CI: 16.611-19.389). After a median follow up duration of 20 months (range: 12-41), the median OS was 18 months (95% CI: 13.420-22.580) in Group 1 and 22 months (95% CI: 18.777-25.223) in Group 2. There was no statistically significant correlation between the number of chemotherapy cycles and PFS (=0.513) or OS (=0.867). The extent of surgical resection was the only independent prognostic factor for both PFS (=0.015) and OS (=0.028) by multivariate analysis. Three grade ≥3 hematologic toxicity were encountered in 3 patients. One in the six-cycle group (neutropenia), and two in the extended cycles group (one had neutropenia and the other one developed thrombocytopenia). No statistically significant difference in the toxicity profile between both groups. The results of our study suggest that extended TMZ therapy is safe and tolerable, however it did not significantly improve PFS or OS as compared to the standard six-cycle course. Larger randomized studies are required to shed more light on this issue.

摘要

尽管同步放化疗及辅助替莫唑胺(TMZ)治疗6个周期已被确立为新诊断多形性胶质母细胞瘤(GBM)患者的标准治疗方案,但辅助TMZ的推荐疗程仍存在争议。在此,我们旨在首次报告来自上埃及地区的经验,通过比较辅助TMZ两种治疗模式(>6个周期与6个周期)的生存情况和毒性特征,并确定在接受放疗联合辅助TMZ治疗的埃及新诊断GBM患者中具有预后意义的因素。2016年6月至2018年2月期间,对121例患者的病历进行回顾性审查以提取研究相关数据。所有患者均接受同步放化疗,随后29例患者(第1组)接受TMZ治疗6个周期,26例患者(第2组)接受TMZ治疗>6个周期。第1组患者的中位无进展生存期(PFS)为15个月(95%CI:10.215 - 19.785),而第2组患者的中位PFS为18个月(95%CI:16.611 - 19.389)。在中位随访20个月(范围:12 - 41个月)后,第1组的中位总生存期(OS)为18个月(95%CI:13.420 - 22.580),第2组为22个月(95%CI:18.777 - 25.223)。化疗周期数与PFS(=0.513)或OS(=0.867)之间无统计学显著相关性。多因素分析显示,手术切除范围是PFS(=0.015)和OS(=0.028)的唯一独立预后因素。3例患者出现3级及以上血液学毒性。6周期组1例(中性粒细胞减少),延长周期组2例(1例中性粒细胞减少,另1例血小板减少)。两组之间毒性特征无统计学显著差异。我们的研究结果表明,延长TMZ治疗是安全且可耐受的,然而与标准的6周期疗程相比,它并未显著改善PFS或OS。需要更大规模的随机研究来进一步阐明这一问题。

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