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Newcastle disease virus enhances the growth-inhibiting and proapoptotic effects of temozolomide on glioblastoma cells in vitro and in vivo.纽卡斯尔病病毒增强替莫唑胺对体外和体内脑胶质瘤细胞的生长抑制和促凋亡作用。
Sci Rep. 2018 Jul 31;8(1):11470. doi: 10.1038/s41598-018-29929-y.
2
Impact of interim progression during the surgery-to-radiotherapy interval and its predictors in glioblastoma treated with temozolomide-based radiochemotherapy.替莫唑胺同步放化疗治疗胶质母细胞瘤时,手术至放疗间期疾病进展的影响及其预测因素
J Neurooncol. 2017 Aug;134(1):169-175. doi: 10.1007/s11060-017-2505-x. Epub 2017 May 25.
3
Temozolomide during radiotherapy of glioblastoma multiforme : Daily administration improves survival.替莫唑胺在多形性胶质母细胞瘤放疗期间:每日给药可提高生存率。
Strahlenther Onkol. 2017 Nov;193(11):890-896. doi: 10.1007/s00066-017-1110-4. Epub 2017 Feb 14.
4
Phase 1/2 trials of Temozolomide, Motexafin Gadolinium, and 60-Gy fractionated radiation for newly diagnosed supratentorial glioblastoma multiforme: final results of RTOG 0513.替莫唑胺、莫替沙芬钆与60Gy分割放疗用于新诊断幕上多形性胶质母细胞瘤的1/2期试验:RTOG 0513的最终结果
Int J Radiat Oncol Biol Phys. 2015 Apr 1;91(5):961-7. doi: 10.1016/j.ijrobp.2014.12.050.
5
Severe cholestatic hepatitis due to temozolomide: an adverse drug effect to keep in mind. Case report and review of literature.替莫唑胺所致严重胆汁淤积性肝炎:一种需谨记的药物不良反应。病例报告及文献综述
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Temozolomide versus procarbazine, lomustine, and vincristine in recurrent high-grade glioma.替莫唑胺对比洛莫司汀、司莫司汀和长春新碱治疗复发性高级别胶质瘤。
J Clin Oncol. 2010 Oct 20;28(30):4601-8. doi: 10.1200/JCO.2009.27.1932. Epub 2010 Sep 20.
7
Effects of radiotherapy with concomitant and adjuvant temozolomide versus radiotherapy alone on survival in glioblastoma in a randomised phase III study: 5-year analysis of the EORTC-NCIC trial.同步放化疗联合辅助替莫唑胺与单纯放疗对胶质母细胞瘤生存影响的随机III期研究:EORTC-NCIC试验的5年分析
Lancet Oncol. 2009 May;10(5):459-66. doi: 10.1016/S1470-2045(09)70025-7. Epub 2009 Mar 9.
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Risk analysis of severe myelotoxicity with temozolomide: the effects of clinical and genetic factors.替莫唑胺致严重骨髓抑制的风险分析:临床与遗传因素的影响。
Neuro Oncol. 2009 Dec;11(6):825-32. doi: 10.1215/15228517-2008-120.
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Phase 2 study of temozolomide and Caelyx in patients with recurrent glioblastoma multiforme.替莫唑胺与凯素(多柔比星脂质体)用于复发性多形性胶质母细胞瘤患者的II期研究。
Neuro Oncol. 2004 Jan;6(1):38-43. doi: 10.1215/S1152851703000188.
10
Temozolomide in patients with glioblastoma at second relapse after first line nitrosourea-procarbazine failure: a phase II study.替莫唑胺用于一线亚硝基脲-丙卡巴肼治疗失败后第二次复发的胶质母细胞瘤患者:一项II期研究。
Oncology. 2002;63(1):38-41. doi: 10.1159/000065718.

接受替莫唑胺方案治疗的患者的毒性反应及相关因素:12 年医院数据分析。

Toxicities and Associated Factors in Patients Receiving Temozolomide-Containing Regimens: A 12-Year Analysis of Hospital Data.

机构信息

Department of Pharmacy, Union Hospital, Tongji Medical College, Huazhong University of Science & Technology (HUST), Wuhan, People's Republic of China.

Hubei Province Clinical Research Center for Precision Medicine for Critical Illness, Wuhan, 430022, People's Republic of China.

出版信息

Drug Des Devel Ther. 2021 May 20;15:2151-2159. doi: 10.2147/DDDT.S305792. eCollection 2021.

DOI:10.2147/DDDT.S305792
PMID:34045849
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8146745/
Abstract

OBJECTIVE

Although temozolomide has been extensively used to treat various tumors, there is a lack of large-cohort studies on temozolomide's toxicity profile. The toxicity profiles and associated factors in patients treated with temozolomide-containing regimens were analyzed.

PATIENTS AND METHODS

Patients treated with temozolomide-containing regimens in the Affiliated Union Hospital of Huazhong University of Science and Technology from January 2008 to December 2019 were included. A retrospective analysis of the clinical data of patients treated with temozolomide-containing regimens was performed. Univariate chi-square test and multivariate logistic regression analysis were employed to identify factors associated with the occurrence of toxicities.

RESULTS

Among the 1057 patients received temozolomide-containing regimens, 922 patients were included in our analyses. Of the 922 patients, 484 patients (52.5%) experienced toxicities. Univariate analysis revealed that radiotherapy, chemotherapy cycle, chemotherapy regimen, and clinical stage were significantly associated with the toxicity during temozolomide treatment ( < 0.05). The chemotherapy regimen, chemotherapy cycle, and clinical stage were significantly associated with the overall occurrence of toxicities ( < 0.05). A chemotherapy regimen, chemotherapy cycle, and clinical stage were associated with the hematological system's toxicities, whereas gender, age, clinical diagnosis, and clinical stage were related to gastrointestinal toxicities ( < 0.05). Clinical diagnosis, chemotherapy regimen, and age were associated with liver toxicity ( < 0.05).

CONCLUSION

Toxicities are common among patients receiving temozolomide-containing regimens. Clinicians should be aware of factors associated with toxicities to minimize the impact of the toxicity.

摘要

目的

替莫唑胺已广泛用于治疗各种肿瘤,但关于其毒性谱的大样本研究较少。本研究旨在分析接受替莫唑胺方案治疗患者的毒性谱及相关因素。

方法

回顾性分析 2008 年 1 月至 2019 年 12 月在华中科技大学同济医学院附属协和医院接受替莫唑胺方案治疗的患者的临床资料,采用单因素 χ2 检验和多因素 logistic 回归分析方法,筛选与毒性发生相关的因素。

结果

共纳入 1057 例接受替莫唑胺方案治疗的患者,其中 922 例纳入本研究。922 例患者中,484 例(52.5%)出现毒性反应。单因素分析显示,放疗、化疗周期、化疗方案和临床分期与替莫唑胺治疗期间的毒性显著相关(<0.05)。化疗方案、化疗周期和临床分期与毒性的总发生率显著相关(<0.05)。化疗方案、化疗周期和临床分期与血液系统毒性相关,而性别、年龄、临床诊断和临床分期与胃肠道毒性相关(<0.05)。临床诊断、化疗方案和年龄与肝毒性相关(<0.05)。

结论

接受替莫唑胺方案治疗的患者常见毒性反应,临床医生应了解与毒性相关的因素,以尽量减少毒性的影响。