Metronomic Temozolomide in Heavily Pretreated Patients With Recurrent Isocitrate Dehydrogenase Wild-type Glioblastoma: A Large Real-Life Mono-Institutional Study

被引:2
作者
Bosio, A. [1 ,2 ]
Cerretti, G. [1 ]
Padovan, M. [1 ,3 ]
Caccese, M. [1 ]
Denaro, L. [4 ]
Chioffi, F. [5 ]
Della Puppa, A. [6 ]
Aldegheri, V. [7 ]
Guarneri, V. [2 ,8 ]
Zagonel, V. [1 ]
Lombardi, G. [1 ]
机构
[1] Veneto Inst Oncol IOV IRCCS, Dept Oncol, Oncol 1, Padua, Italy
[2] Univ Padua, Dept Surg Oncol & Gastroenterol DiSCOG, Padua, Italy
[3] Univ Padua, Dept Surg Oncol & Gastroenterol, Clin & Expt Oncol & Immunol PhD Program, Padua, Italy
[4] Univ Padua, Dept Neurosci, Acad Neurosurg, Padua, Italy
[5] Azienda Osped Univ Padova, Neurosurg Unit, Padua, Italy
[6] Azienda Osped Univ Careggi, Neurosurg Unit, Florence, Italy
[7] Veneto Inst Oncol IOV IRCCS, Radiol Unit, Padua, Italy
[8] Ist Oncol Veneto IRCCS, Div Oncol 2, Padua, Italy
关键词
Chemotherapy; glioblastoma; IDH; metronomic temozolomide; PHASE-II TRIAL; LOW-DOSE TEMOZOLOMIDE; ADJUVANT TEMOZOLOMIDE; RADIOTHERAPY; METHYLATION; CONCOMITANT; BIOMARKER; EFFICACY;
D O I
10.1016/j.clon.2023.01.012
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Aims: Glioblastoma (GBM) is the most common primary malignant brain tumour in adults and frequently relapses. The aim of this study was to assess the efficacy and safety of metronomic temozolomide (TMZ) in the recurrent GBM population.Materials and methods: All patients treated at our centre between September 2013 and March 2021 were retrospectively reviewed. The main inclusion criteria were first-line therapy with the Stupp protocol, relapse after the first or subsequent line of therapy, treatment with a metronomic TMZ schedule (50 mg/m2 continuously) and histological diagnosis of isocitrate dehydrogenase wild-type GBM according to World Health Organization 2016 classification.Results: In total, 120 patients were enrolled. The median follow-up was 15.6 months, the median age was 59 years, Eastern Cooperative Oncology Group performance status (ECOG-PS) was 0-2 in 107 patients (89%). O6-methylguanine-DNA-methyltransferase (MGMT) was methylated in 66 of 105 (62%) evaluable patients. The median number of prior lines of treatment was 2 (range 1-7). Three (2%) patients showed a partial response; 48 (40%) had stable disease; 69 (57%) had progressive disease. The median overall survival from the start of metronomic TMZ was 5.4 months (95% confidence interval 4.3-6.4), whereas the median progression-free survival (PFS) was 2.6 months (95% confidence interval 2.3-2.8). At univariate analysis, MGMT methylated and unmethylated patients had a median PFS of 2.9 and 2.1 months (P = 0.001) and a median overall survival of 5.6 and 4.4 months (P = 0.03), respectively. At multivariate analysis, the absence of MGMT methylation (hazard ratio = 2.3, 95% confidence interval 1.3-3.9, P = 0.004) and ECOG-PS <= 2 (hazard ratio = 0.5, 95% confidence interval 0.3-0.9, P = 0.017) remained significantly associated with PFS, whereas ECOG-PS <= 2 (hazard ratio = 0.4, 95% confidence interval 0.3-07, P = 0.001) was the only factor associated with overall survival. The most common grade 3-4 toxicities were haematological (lymphopenia 10%, thrombocytopenia 3%).Conclusions: Rechallenge with metronomic TMZ is a well-tolerated option for recurrent GBM, even in pretreated patients. Patients with methylated MGMT disease and good ECOG-PS seem to benefit the most from this treatment.(c) 2023 The Author(s). Published by Elsevier Ltd on behalf of The Royal College of Radiologists. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
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收藏
页码:e319 / e327
页数:9
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